key: cord-294700-pb5k21da
authors: Dulek, Daniel E; Fuhlbrigge, Robert C; Tribble, Alison C; Connelly, James A; Loi, Michele M; El Chebib, Hassan; Chandrakasan, Shanmuganathan; Otto, William R; Diorio, Caroline; Keim, Garrett; Walkovich, Kelly; Jaggi, Preeti; Girotto, Jennifer E; Yarbrough, April; Behrens, Edward M; Cron, Randy Q; Bassiri, Hamid
title: Multidisciplinary Guidance Regarding the Use of Immunomodulatory Therapies for Acute COVID-19 in Pediatric Patients
date: 2020-08-18
journal: J Pediatric Infect Dis Soc
DOI: 10.1093/jpids/piaa098
sha: 
doc_id: 294700
cord_uid: pb5k21da

BACKGROUND: Immune-mediated lung injury and systemic hyperinflammation are characteristic of severe and critical coronavirus disease 2019 (COVID-19) in adults. Although the majority of SARS-CoV-2 infections in pediatric populations result in minimal or mild COVID-19 in the acute phase of infection, a small subset of children develop severe and even critical disease in this phase with concomitant inflammation that may benefit from immunomodulation. Therefore, guidance is needed regarding immunomodulatory therapies in the setting of acute pediatric COVID-19. This document does not provide guidance regarding the recently emergent multisystem inflammatory syndrome in children (MIS-C). METHODS: A multidisciplinary panel of pediatric subspecialty physicians and pharmacists with expertise in infectious diseases, rheumatology, hematology/oncology, and critical care medicine was convened. Guidance statements were developed based on best available evidence and expert opinion. RESULTS: The panel devised a framework for considering the use of immunomodulatory therapy based on an assessment of clinical disease severity and degree of multi-organ involvement combined with evidence of hyperinflammation. Additionally, the known rationale for consideration of each immunomodulatory approach and the associated risks and benefits was summarized. CONCLUSIONS: Immunomodulatory therapy is not recommended for the majority of pediatric patients, who typically develop mild or moderate COVID-19. For children with severe or critical illness, the use of immunomodulatory agents may be beneficial. The risks and benefits of such therapies are variable and should be evaluated on a case-by-case basis with input from appropriate specialty services. When available, the panel strongly favors immunomodulatory agent use within the context of clinical trials. The framework presented herein offers an approach to decision-making regarding immunomodulatory therapy for severe or critical pediatric COVID-19 and is informed by currently available data, while awaiting results of placebo-controlled randomized clinical trials.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a recently emergent human pathogen that causes a variety of disease manifestations termed Coronavirus Disease 2019 . The spectrum of COVID-19 ranges from asymptomatic infections to severe and critical illness with multi-organ involvement that can prove fatal [1] . In adults, the most common disease presentation involves respiratory disease that either resolves or evolves into progressive pulmonary involvement and acute respiratory distress syndrome (ARDS); in adult patients with progressive disease, extrapulmonary manifestations and evidence of multi-organ involvement is common. While severe and critical COVID-19 is substantially more prevalent in adults, a small proportion of children also develop progressive respiratory disease and concomitant multi-organ dysfunction with high morbidity, but fatalities are rarely reported [2] [3] [4] [5] . Comorbid conditions for this presentation of severe and critical COVID-19 in adults include obesity, diabetes, and underlying cardiac disease [6, 7] however, such risk factors are currently not well defined in children [3, 5, 8] .

Initial descriptions of COVID-19 presentations and outcomes indicate a substantial inflammatory component to severe disease [9] [10] [11] . Inflammatory phenotypes include significant pulmonary inflammation accompanied by prolonged fevers [12] and/or a biphasic illness course characterized by initial improvement followed by rapid occurrence of respiratory failure and pulmonary inflammation [10, 13] . In addition, COVID-19-associated cardiac injury is an independent risk factor for mortality, suggesting that inflammation beyond lung parenchyma contributes to poor outcomes [14, 15] . Further, severe COVID-19 is associated with more significant lymphopenia, systemically elevated pro-inflammatory cytokine levels, and impaired CD4+ T cell IFN-γ expression compared to moderate COVID-19 [11] .

These early reports of hyperinflammation are reminiscent of the cytokine storm features described in the setting of prior emergent respiratory virus infections including SARS (2002), Middle East Respiratory Syndrome (MERS), H5N1 avian influenza, and 2009 H1N1 pandemic influenza [16, 17] . In each of these viral infections, significant pulmonary and systemic inflammation was identified and, in some cases, linked to poor outcomes and mortality (SARS [18] [19] [20] [21] ; avian influenza [22, 23] ;

2009 H1N1 [24] [25] [26] ; MERS [27] [28] [29] ). Since the initial SARS outbreak in 2002, several developments have changed the paradigm for treatment of hyperinflammation. First, detailed mechanistic knowledge of the genetics and immunopathology of macrophage activation syndrome (MAS) and hemophagocytic lymphohistiocytosis (HLH) have led to targeted treatments for cytokine storm syndrome (CSS) [30] . In addition, new immunomodulators targeting specific cytokines, cytokine receptors, and immune pathways have been developed and studied in a wide variety of other A c c e p t e d M a n u s c r i p t 5 inflammatory and autoimmune diseases [31, 32] . Finally, the advent of chimeric antigen receptor (CAR) T cell therapy for leukemia/lymphoma and resultant cytokine release syndrome (CRS) has provided a specific example of cytokine-targeted therapy leading to rapid clinical improvement in the setting of marked and hyperacute inflammation [33] .

Symptoms of severe COVID-19 in children as currently reported fall into two categories. In a small subset of pediatric patients, severe lung disease occurs and appears to mimic severe adult COVID-19 with respiratory failure, ARDS, and associated multi-organ failure [5] . In other pediatric patients, an emerging inflammatory disease has recently been described [34] [35] [36] This latter presentation has been variably called PIMS-TS [37] , PMIS [38] , and MIS-C [39] and manifests as acute onset of fever with multisystem involvement, frequently including hypotension and cardiac dysfunction in the absence of respiratory symptoms. Some reported cases mimic severe Kawasaki disease or Toxic Shock syndrome phenotypes. MIS-C appears to be associated with prior exposure to SARS-CoV-2. Although immune modulation with corticosteroids and intravenous immunoglobulin (IVIG) is used in severe cases of MIS-C [36] , given the very limited information about the mechanisms of this disease process, in this document we do not provide specific guidance for treatment of this syndrome.

Anecdotal reports of immunomodulator use in the setting of COVID-19 have been widespread [40] [41] [42] [43] [44] . While numerous trials of immunomodulatory therapies for COVID-19 in adults are being launched, few clinical trials for immunomodulatory therapy in pediatric patients with COVID-19 are currently enrolling or planned. Therefore, we undertook a comprehensive review of the current state of literature regarding immunomodulatory therapy in COVID-19. The goal for this document is to provide pediatric practitioners a framework for interpreting currently available data and a rationale for considering immunomodulatory therapy in the care of pediatric acute COVID -19 patients. In the sections below, cytokine storm, CSS, and hyperinflammation are used interchangeably to refer to the pulmonary and systemic inflammation that accompanies severe and critical COVID-19. This review does not represent a final or definitive guideline for diagnosis or treatment, but a review of current knowledge, and we emphasize the importance of enrollment in clinical trials for COVID-19 immunomodulatory therapy when available.

A c c e p t e d M a n u s c r i p t 6

A multidisciplinary panel of pediatric subspecialty physicians and pharmacists with expertise in infectious diseases, rheumatology, hematology/oncology, and critical care medicine was convened.

We relied on the guidance approach recently published addressing antiviral use in children with COVID-19 [45] . Guidance statements were developed based on best available evidence and expert opinion. Given the lack of currently available randomized controlled trials for the therapies considered in this document and the overall limited nature of the data, a systematic review was not performed, nor was evidence formally evaluated using Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) or other methodology.

As previously described [45] , we used the following definitions and similarly assert the importance of "first do no harm" in the consideration of proposed immunomodulatory therapies with yet unknown efficacy in the setting of COVID-19. Statements using the term "suggest" indicate the panel's view that currently available evidence is weighted towards risk or benefit from a proposed therapy.

Guidance statements of "consider" reflect uncertainty by the panel with regard to risk or benefit of a proposed therapy.

The panel considered three major questions related to immunomodulatory therapy for children with COVID-19:

1. Are immunomodulatory agents indicated in children with COVID-19?

2. What criteria define the pediatric population in whom immunomodulatory therapy may be considered?

3. What agents, if any, are preferred if immunomodulatory therapy is considered for children with COVID-19?

In addressing these questions, we utilize the definitions of severe and critical COVID-19 previously published (Table 1 ) [45] . We provide background information for several categories of immunomodulatory therapies that have been proposed for potential use in caring for severely or critically ill COVID-19 patients. These categories include IL-1 inhibitors, IL-6 inhibitors, glucocorticoids, convalescent plasma, Janus kinase inhibitors, intravenous immunoglobulin (IVIG), and interferons. Within each section we provide a guidance statement followed by rationale and an A c c e p t e d M a n u s c r i p t 7 evidence summary. In vitro and animal model data is reviewed in selected sections, though we do not significantly address SARS-CoV-2 animal models given a current lack of such published data. In addition, we provide information regarding potential adverse events and practical guidance regarding dosing within each section. A summary of key guidance statements is provided in Table 2 .

Guidance statement:

We emphasize that the vast majority of children with COVID- 19 

The aforementioned antiviral guidance document provided key rationale for consideration of therapies beyond supportive care in children with COVID-19 [45] . Multiple studies and experience in a variety of settings have demonstrated that the majority of children with COVID-19 recover without immunomodulatory interventions and do not develop severe manifestations. Given the lack of available results from randomized-controlled trials of immunomodulatory therapy in children with COVID-19, the risk-benefit ratio for most pediatric patients points toward supportive care as the key management strategy. However, a subset of pediatric patients develops severe or critical illness with acute COVID-19 [5] . It is therefore possible that immunomodulation is a key part of treatment strategy for such patients.

Guidance statement:

We suggest that immunomodulatory therapy only be used for pediatric patients in the setting of confirmed critical COVID-19 (SARS-CoV-2 RT-PCR positive) with evidence of hyperinflammation (Table   4 ). In addition, pediatric COVID-19 patients with hyperinflammation whose pace of illness progression suggests imminent progression to critical COVID- 19 Based on currently available data, very few pediatric patients with COVID-19 will become severely or critically ill [2] [3] [4] 46] . Therefore, for the majority of pediatric COVID-19 patients the risks of immunomodulatory therapy outweigh potential benefits. However, in pediatric patients with critical COVID-19 (defined previously; Table 1 , [45] ), or who are rapidly progressing towards this category, the potential benefits of immunomodulatory therapy may offset the potential risks. In addition, given the potential risks of immunomodulatory therapy, consideration of this therapy in the setting of severe or critical acute COVID-19 should be reserved for patients with RT-PCR-confirmed infection. We are aware that there may be a subset of patients for whom there is a high suspicion of acute COVID-19 despite negative RT-PCR testing. Given the difficulties in determining disease etiology and defining benefits of immunomodulatory therapy, we do not provide specific guidance for this scenario. In the evidence summary below, we review the current data on immunopathology in severe and critical COVID-19 and discuss potential clinical and laboratory criteria on which to base the decision to use immunotherapy.

Adult patients severely affected by COVID-19 demonstrate a variety of overlapping phenotypes of severity including features of ARDS, hypercoagulability, hyperinflammation/CSS, and multi-organ failure [9] [10] [11] . Currently published cohorts indicate that a very large percentage of COVID-19 affected children do well after infection with SARS-CoV-2. Despite these overall reassuring findings in children, reports have emerged that a small subset of pediatric patients are severely affected by COVID-19 with a presentation/severity similar to that seen in adult patients [3, 5, 8, 47] .

The clinical and laboratory presentation of patients with severe acute SARS-CoV-2 infection has revealed similarities and differences with CSS. CSS is associated with dysregulated, inappropriate, and unbalanced immune responses that include enhanced production of proinflammatory cytokines (Table 3 ). CSS is driven by excessive activation of both innate (monocytes, macrophages, neutrophils, NK cells) and adaptive immune cells (T-cells) and overproduction of pro-inflammatory cytokines that produce a recognizable clinical and laboratory pattern of tissue pathology. In general, CSS is associated with evidence of aberrant systemic inflammation including elevated ferritin, low fibrinogen, cytopenias, hemophagocytosis, and variable occurrence of coagulopathy, NK cell dysfunction, and pulmonary, liver, spleen and/or CNS involvement [30] . Current reports of severely and critically ill COVID-19 patients indicate that aberrant and dysregulated inflammation contributes to morbidity and mortality in these patients.

A c c e p t e d M a n u s c r i p t 9 However, parsing out contributions from ARDS, cytokine storm, secondary infections, and coagulopathy/hypercoagulability in the laboratory findings associated with severe/critical COVID-19 remains difficult. In addition, there is likely to be distinct pathophysiology between severe/critical COVID-19 with CSS compared to other categories of CSS. Therefore, we emphasize caution in the application of diagnostic criteria used in other CSS to the assessment of CSS in the setting of COVID-

Current information regarding immunopathogenesis of CSS in acute COVID-19 derives primarily from adult data. We have summarized much of this data below within each specific immunotherapeutic section. Briefly, a subset of patients progress to severe lung injury and death.

Autopsy studies demonstrate exudative diffuse alveolar damage with significant capillary congestion and microthrombi [48] and an association with venous thromboembolism in non-pulmonary sites [49] . Laboratory evidence of markedly elevated inflammation including elevated ferritin, CRP, and ESR values is also noted in severe/critical COVID-19 cases [50] . Further, many patients critically ill with COVID-19 demonstrate evidence of coagulopathy including significantly elevated D-dimer [51] .

Cytokine profiling of patient samples has been performed in adult and pediatric patients.

Elevation in other cytokines/chemokines associated with hyperinflammation states, including CXCL-9

(MIG), CXCL-10 (IP-10), CCL-7 (MCP-3), and IL-1Ra have also been shown [52] . Single cell immune profiling demonstrates an inflammatory signature that includes significant inflammatory gene expression with classical monocytes [53] . Furthermore, several early studies have suggested a link between impaired innate interferon expression and development of excessive inflammation in COVID-19 patients [54] [55] [56] [57] . Based on this data, several cohorts reporting use of immunomodulation in COVID-19 have been recently published [42, [58] [59] [60] [61] . These manuscripts and related reports are reviewed in specific sections below.

The panel recommends that use of immunomodulatory therapy for the treatment COVID-19 related hyperinflammation/ cytokine storm should be conducted in the context of a clinical trial, if available. In the absence of such opportunity, and recognizing that definitive evidence is lacking, consideration for use of immunomodulatory agents in cases of SARS-CoV-2 infection with clinical and biochemical evidence of cytokine storm physiology (e.g., features of secondary HLH) should be limited to patients with clear evidence of critical COVID-19 disease and risk for multi-organ failure. In this restricted scenario, an experimental approach using immunotherapy has theoretical potential for benefit and is supported by increasing evidence, as detailed below. We propose several key categories of clinical information to consider regarding the use of immunomodulatory therapy for pediatric COVID-19 patients (Table 4 ). These include clinical and laboratory illness features and A c c e p t e d M a n u s c r i p t 10 take into account the pace of illness progression, evidence of organ injury/impending organ failure, and evidence of hyperinflammation. Importantly, given the current state of knowledge and lack of available clinical trial results, we are not able to provide specific cutoffs or laboratory results that indicate a definite need for immunomodulatory therapy.

Although current literature has identified proposed laboratory findings demonstrating hyperinflammation as indicators of risk for severe/critical COVID-19, these are not validated and individual values should be assessed in the context of the patient's overall status. No single feature or laboratory value is known to be sufficient to recommend immunotherapy. However, it is anticipated that timely recognition and intervention could improve outcomes, such that trends toward worsening disease and the cadence of change should be considered. Despite the overlap with CSS and noted elevations in inflammatory markers and pro-inflammatory cytokines, diagnostic criteria for familial HLH (fHLH), MAS, and CRS should not be necessarily be used to identify COVID-19 patients who may benefit from immune suppression or immune modulation, as these definitions are likely to differ for SARS-CoV-2 infections, just as they do between the different CSS categories.

Consideration for use of experimental therapies should entail discussion between the patient's primary team and appropriate consulting teams with experience in the use of immunomodulatory drug treatment in the setting of infection including infectious diseases, rheumatology, and/or hematology/oncology, critical care, and with involvement of pharmacists.

Further, use of these therapies should be performed only with appropriate counseling and consenting of patients and families for off-label use of immune modulatory medications according to each individual institution's policies.

Guidance statement:

There are no immunomodulators with proven efficacy for the treatment of COVID-19 in pediatric patients as of 24 July 2020. Therefore, no guidance can be provided to support the use of one immunomodulatory therapy over another. 

As outlined in topic-specific sections below, there are no randomized, controlled trials evaluating the use of immunomodulatory therapies in pediatric COVID-19 patients. Numerous cohort studies have recently been published though many of these are limited by absence or inadequacy of a rigorous comparator group. A few randomized controlled trials have recently been published. However, none of these provides comparison between immunomodulatory agents. Therefore, the current state of evidence does not allow for selection of one immunomodulatory therapy over another. As with the decision to use or not use an immunomodulator in a pediatric COVID-19 patient, the choice of which immunomodulatory therapy to use should be driven by an individualized weighing of potential risks and potential benefits. In addition, though superseded by evidence of efficacy and adverse effects, relative drug availability and cost may play a role in immunomodulatory therapy choice. For each immunomodulatory therapy addressed below, we provide rationale, evidence summary, potential risks, and practical considerations to assist in these individualized patient care decisions. The order of discussion of immunomodulatory therapies below does not reflect any preference for one category over another.

Guidance statement:

given to clinical trial enrollment if available.

The effects of IL-6 can be inhibited by blocking binding to the IL-6 receptor using monoclonal antibodies such as tocilizumab, siltuximab, and sarilumab. Notably, these are each being tested for use in COVID-19 in over a dozen clinical trials that are currently recruiting patients. Given that the pediatric experience with IL-6 inhibition has mostly been with use of tocilizumab, the panel would favor use of this agent, should this therapeutic modality be considered, although other agents may also be considered in select situations (e.g. anaphylaxis with tocilizumab or drug shortages).

A c c e p t e d M a n u s c r i p t 12 Tocilizumab is FDA approved (albeit not for this indication), and dosing data are extrapolated from that used in CSS following CAR T cell or blinatumomab therapy.

Mechanism and current uses: IL-6 is a pleiotropic cytokine produced by a number of nonhematopoietic cells and cells of myeloid origin during infections and in response to tissue injury. IL-6 binds its receptor (IL-6R) and initiates a JAK/STAT-mediated signaling pathway, which results in transcription of numerous genes [62] . Increased IL-6 levels are observed in a number of viral infections, and in animal models elevated IL-6 levels favor the persistence of some of these viruses [63] [64] [65] [66] . Tocilizumab is currently FDA approved for the treatment of CAR T cell-induced CRS in both children and adults, rheumatoid arthritis and giant cell arteritis in adults, as well as polyarticular and systemic juvenile idiopathic arthritis in children [67] .

In vitro and animal data: A number of prior in vitro studies demonstrated that infection of airway epithelial cells or macrophages [68, 69] with either SARS or MERS coronaviruses could elicit production of IL-6 and TNF-; similar results were also observed with purified coronavirus spike (S) or nucleocapsid (N) proteins [70, 71] . In an animal model, primary infection with SARS is associated with an IL-6 gene signature and an associated self-sustaining acute phase response [72] .

Human data: Several studies have examined the cytokine response to SARS-CoV-2; these have demonstrated the presence of mild to moderately elevated IL-6 in serum or plasma of adult and pediatric COVID-19 patients [11, 17, 73] . Moreover, the levels of IL-6 transcript and protein appear to correlate with the severity of COVID-19 and mortality in adults [50, 73, 74] . A proportion of pediatric COVID-19 patients were also shown to possess similarly elevated IL-6 levels [75] . While blinded and randomized clinical trial data are still needed, several recently published cohort studies have indicated mixed evidence for benefit for tocilizumab in adult COVID-19 patients. In a single center cohort study of adult COVID-19 patients requiring mechanical ventilation, treatment with tocilizumab was associated with decreased mortality with a hazard ratio (HR) for death of 0.55 (95% CI 0.33-0.9) after adjusting for disease severity at tocilizumab initiation [76] . Similarly, in an Italian multicenter retrospective cohort study of 544 severe COVID-19 adult patients, tocilizumab treatment was associated with decreased risk of mechanical ventilation or death (adjusted HR 0.61; 95% CI 0.4-0.92) [77] . These results are supported by several smaller cohorts [42, 61, [78] [79] [80] [81] [82] A c c e p t e d M a n u s c r i p t 13 Potential Risks:

While it is generally recommended that tocilizumab not be initiated in patients with neutropenia or thrombocytopenia or in those with elevations of alanine aminotransferase or aspartate aminotransferase, in practice many patients with severe or life-threatening systemic inflammatory response syndrome (SIRS) experience cytopenias or elevated transaminases due to multi-system organ dysfunction or the use of concurrent medications. Therefore, it may be reasonable to cautiously initiate tocilizumab therapy in such patients with close monitoring.

Additionally, tocilizumab therapy may increase risk of bacterial and mycobacterial infections (especially the reactivation of M. tuberculosis), viral reactivation (especially hepatitis B), and invasive fungal disease [67] . Notably most of these reports are from adults (e.g. those with rheumatoid arthritis) who have received chronic IL-6 inhibition and, therefore, risk for children on shorter courses of tocilizumab may not be as significant. Interestingly, the above cited studies have shown an increase in superinfection in patients treated with tocilizumab though without clear impact on outcomes [76, 77] . Other adverse events such as pneumatosis intestinalis and intestinal perforation [83] , hepatic injury and liver failure [84] , hypertriglyceridemia and pancreatitis [85] have also been reported.

Note that dosing for tocilizumab in pediatric populations is largely based on use for rheumatologic indications and in CAR T cell-associated CRS [28, 32] . The suggested intravenous (iv) dosing is 12mg/kg for patients with a total body weight less than 30kg and 8mg/kg for those 30kg and above, with a maximum dose of 800mg. Monitoring for anaphylaxis should be performed and, if noted, should be treated using standard local protocols. Additionally, periodic laboratory (e.g. complete blood counts (CBCs), hepatic and pancreatic function testing, etc.) and clinical exam monitoring is suggested. Of note, while tocilizumab does not directly affect the P450 cytochrome system, elevated levels of IL-6 can inhibit these enzymes, and thus drugs that are metabolized by this system may also require monitoring. The half-life of tocilizumab is concentration dependent and is estimated to be up to 2 weeks in high-dose therapy (as suggested for use in COVID-19 hyperinflammation) of adult patients receiving chronic therapy at 8mg/kg every 4 weeks. Most adult studies of COVID-19-associated hyperinflammation use a single dose with some studies providing two doses separated by 12-24 hours if there is lack of response to the first dose. Finally, since tocilizumab blocks the IL-6 receptor, following IL-6 levels is not useful for monitoring and is not recommended.

A c c e p t e d M a n u s c r i p t 14

Guidance statement:

given to clinical trial enrollment if available. If IL-1 inhibition is used as a treatment modality for pediatric COVID-19 patients, we suggest the use of anakinra based on its safety profile and favorable pharmacokinetics.

Available data from the prior SARS and MERS outbreaks and early data from the current SARS-CoV-2 pandemic suggest that IL-1β may play a role in SARS-CoV-2-related immunopathology.

Evidence that inhibition of IL-1-signaling may safely improve outcomes in COVID-19 [58] [59] [60] 86] . 

Mechanism and current uses: IL-1α and IL-1β are two of the 11 members (including IL-18 and IL-33) of the IL-1 cytokine family and play a critical role in a wide variety of pro-inflammatory states. IL-1β is the major biologically active and secreted form in the setting of infection and other inflammation, but IL-1α is likely released by dying endothelial cells. IL-1β exerts its effects through binding to its specific receptor subunit IL-1R1 followed by co-receptor recruitment. Biological effects of IL-1β include recruitment of endothelial adhesion molecule expression and inflammatory cell recruitment, upregulation of prostaglandins and nitric oxide, and metalloproteinase production. Systemically, IL-1β contributes to hypotension, fever, neutrophilia, and other acute phase responses. Importantly, IL-1β contributes to CD4+ Th17 differentiation by contributing to key aspects of transcriptional activation [88] . IL-1 can also act upstream to increase IL-6 expression [89] .

Several targeted therapies inhibit IL-1β signaling including anakinra, a recombinant form of IL-1 receptor antagonist (IL1-Ra) which mimics native IL-1Ra and prevents binding of IL-1α and IL-1β A c c e p t e d M a n u s c r i p t 15 to IL-1R1 and thereby prevent IL-1-mediated immune effects [90] . Another IL-1 targeting drug, rilonacept, binds and neutralizes both IL-1α and IL-1β. In addition, a monoclonal antibody, canakinumab, binds IL-1β and prevent its interaction with IL-1R1 [91] . Anakinra is FDA approved for adults with rheumatoid arthritis who have failed one or more disease modifying antirheumatic drug (DMARD) and for the treatment of Neonatal Onset Multisystem Inflammatory Disease (NOMID).

Randomized controlled trials of each of the medications have demonstrated their safety with infections occurring infrequently when used in these settings [92] [93] [94] [95] [96] [97] [98] .

Anakinra has been best studied in terms of treating other CSS, including macrophage activation syndrome and secondary hemophagocytic lymphohistiocytosis. It is a recombinant human protein with over 7,000 patient-years of favorable safety data. Anakinra has a short half-life of 4-6 hours, can be given intravenously or subcutaneously, and works quickly. Anakinra also has a wide therapeutic window (effective with minimal adverse effects reported from 1-48 mg/kg/day, including use in patients with sepsis). Retrospective analysis of a large randomized clinical trial demonstrated that anakinra improved survival in sepsis patients with features of CSS (hepatobiliary dysfunction and disseminated coagulopathy) from 35% (placebo) to 65% [99] . An early case series of pediatric rheumatic disease patients with refractory CSS reported resolution in 12 out of 12 patients treated with anakinra [100] . More recently, a retrospective report of 44 children with rheumatologic, oncologic, and infectious etiologies of CSS reported 73% survival rate for those who received anakinra at any point during their hospitalization [101] . Further, anakinra has also been touted to effectively treat CSS in children requiring intensive care [102] .

Importantly, for interpreting results and studies summarized below, measurement of IL-1β

in peripheral blood compartments such as plasma and serum may not accurately reflect its biological activity in a variety of disease states. This is likely due in part to its short half-life and tight regulation of IL-1β's activity in human immune responses via soluble-IL-1 receptors and IL-1Ra, among other regulators [103] .

In vitro and animal data: Several SARS proteins (E protein, Protein 3a, and ORF8b) are shown in in vitro studies to activate the NLRP3 inflammasome. Protein 3A and E protein each activate the NLRP3 inflammasome in LPS-primed mouse bone marrow derived macrophages and African green monkey kidney-derived vero cells, respectively [104] [105] [106] [107] .

A c c e p t e d M a n u s c r i p t 16 Human data: An association between IL-1β and SARS-associated immunopathology was made predominantly through measurement of serum/plasma IL-1β levels in SARS-CoV-1 infected patients.

In general, these studies are limited by a lack of control groups and/or measurement of IL-1β at few or inconsistent time points post-infection [19, [108] [109] [110] . Immunohistochemistry of lung sections from autopsy specimens of four SARS patients did demonstrate elevated IL-1β expression in SARSinfected cells [111] .

Following several small case series [58, 60] , two retrospective cohort studies have shown potential benefit for anakinra in the context of severe COVID-19. Adult COVID-19 patients with moderate to severe ARDS and evidence of hyperinflammation (CRP ≥100mg/L or ferritin ≥900ng/mL) were treated with either iv or subcutaneous anakinra [112] . Comparison between the 29 subjects in the high dose iv anakinra treatment group and historical controls indicated improved survival in the treatment group at 21 days post treatment initiation (90%, anakinra; 50% standard, p=0.09) though mechanical ventilation free survival differences were not statistically significant. No differences in bacteremia rates or frequency of hepatic transaminase elevation were noted [112] . In a separate study in France, 52 adult patients with severe COVID-19 treated with subcutaneous anakinra were compared to 44 historical controls [86] . Anakinra-treated subjects had significant decreased frequency of the primary composite outcome of death or intensive care unit admission for mechanical ventilation (25% versus 73%) with difference remaining significant on multivariate analysis (HR 0.22; 95% CI 0.1-0.49). Thus, anakinra appears to be safe and may provide mortality benefit in the treatment of adult COVID-19 patients. Randomized clinical trials are needed to validate these findings.

Adverse effects of anakinra are difficult to distinguish versus effects of the disease processes being treated but include hematologic suppression, infections, hypersensitivity reactions, and malignancies. Those most commonly reported in pediatric studies include increased liver enzymes, which are usually self-limiting, but a few cases of acute liver failure have been reported. In addition, severe injection site reactions and cytopenias have been reported [113, 114] . Importantly for the discussion of high versus standard dose anakinra below, high dose anakinra was associated with increased risk of serious bacterial infection in a pooled analysis of studies enrolling adults with RA [115] . Though the majority of studies of anakinra have been performed using subcutaneous (SC) dosing route, iv administration is evolving as an option for the treatment of critically ill patients [99, 116, 117] . The potential utility of iv anakinra in COVID-19 patients is highlighted by the above cited study in which low dose SC anakinra (100 mg twice daily in adult patients) did not produce either significant clinical or laboratory changes in a small subset of COVID-19 patients while the 5 mg/kg IV over 1 hour administered every 12 hours was associated with sustained clinical benefit [112] .

Despite these encouraging results, stability data for iv anakinra are incomplete and caution is warranted in the use of iv anakinra.

As noted above, measurement of IL-1 levels in peripheral blood is difficult and therefore not recommended during anakinra administration. For toxicity, close monitoring of AST and ALT should be performed as these can become elevated on anakinra therapy. In general, hepatic transaminase elevation resolves with discontinuation or lowering of dose. CBC with differential should be monitored to evaluate for anakinra-induced leukopenia and/or thrombocytopenia. Though increased infections are a reported risk with the use of anakinra, anakinra has a low rate of secondary infection risk and a long record of safety in clinical practice [115, 118, 119] . In the use of anakinra in COVID-19, tuberculosis screening is not needed to initiate therapy because of clinical urgency for therapy initiation.

Guidance statement:

Given their pleiotropic effects, glucocorticoids are used in a variety of inflammatory conditions and settings. As such, it is difficult to definitively support or discourage the use of glucocorticoids in all situations. Therefore, we have provided guidance for specific situations in the following section.

Given the concerns over immune dysregulation associated with COVID-19, glucocorticoids have been proposed and used as a potential treatment modality [120] [121] [122] . Glucocorticoids regulate the immune system in a broad and multimodal manner and block multiple signaling pathways that propagate inflammatory signals [123, 124] . During the early phase of the immune response, glucocorticoid-glucocorticoid receptor complexes attenuate the signaling of Toll-like receptors, inhibit the production of numerous pro-inflammatory cytokines [125] , and dampen cytokine signaling [126] . Glucocorticoids also have a potent effect on cellular immunity, especially T cell A c c e p t e d M a n u s c r i p t 18 signaling and activation [127] . Overall, glucocorticoids are one potential therapeutic option for the treatment of COVID-19, but benefits offered by glucocorticoids in attenuating immune dysregulation must be balanced with their inhibitory effect on the immune response needed to control viral replication as well as the risk of opportunistic infections and associated side-effects. Glucocorticoids, however, are available readily and at low cost.

Given the numerous clinical uses for glucocorticoids and mechanisms by which they impact the immune system, we have limited this evidence summary to address prior data from SARS, and currently available data from COVID-19.

Data regarding the efficacy of glucocorticoids in the treatment of SARS are difficult to interpret. Glucocorticoids were frequently used as part of many treatment protocols, each with different dosing regimens and varied times of treatment initiation; thus most studies did not contain placebo arms [128] [129] [130] [131] [132] [133] [134] [135] [136] [137] . A systematic review of the treatment effects of multiple therapeutic modalities for SARS, including glucocorticoids, revealed that 13/15 studies examining the effect of steroids were inconclusive [138] . No studies showed clear benefit, and 2 studies showed possible harm. Ultimately, the authors concluded that "it is difficult to make a clear recommendation about whether [glucocorticoids] should be used to treat SARS-associated lung injury in any stage of illness, particularly as the drug is immunosuppressive and may delay viral clearance if given before viral replication is controlled" [138] .

Peer-reviewed data evaluating the impact of steroids on COVID-19 treatment outcomes is limited, and comparative data is lacking. Glucocorticoids have been used frequently in critically ill patients [13, 139, 140] . One retrospective cohort study of 201 adult patients with COVID-19 identified risk factors for the development of ARDS and death from ARDS [141] . Sixty-two patients received methylprednisolone, but there were limited data on the dose and timing of initiation of therapy. For those patients with ARDS, treatment with methylprednisolone reduced the risk of death (hazard ratio, 0.38; 95% confidence interval, 0.20-0.72). However, these data should be interpreted with caution due to small sample size and risk of bias.

An additional retrospective cohort study performed in a multicenter health system in Michigan showed potential benefit of early methylprednisolone initiation (median time to initiation of 2 days post admission, IQR 1-3 days) compared to a standard of care cohort with later corticosteroid initiation (median time to initiation of 5 days with IQR of 3-7 days). In this study, early A c c e p t e d M a n u s c r i p t 19 corticosteroid initiation was associated with decreased occurrence of escalation of care to ICU, mechanical ventilation, or death (adjusted OR 0.41; 95% CI 0.22-0.77) [142] .

Recently, data from the RECOVERY Trial, a randomized clinical trial evaluating the impact of treatment with dexamethasone in adults infected with SARS-CoV-2, were published [143] . A total of 6,425 adults were enrolled, and 2,104 patients received 6 mg of dexamethasone daily for up to 10 days. For the primary outcome of 28-day mortality, receipt of dexamethasone was associated with a significant decrease in mortality for those patients receiving invasive mechanical ventilation (29% versus 41%, rate ratio 0.64, 95% confidence interval 0.51 to 0.81) or for those patients who received supplemental oxygen but not mechanical ventilation (23% versus 26%, rate ratio 0.82, 95% confidence interval 0.72 to 0.94). Receipt of dexamethasone was also associated with lower risk of progression to invasive mechanical ventilation, and patients in the dexamethasone group had a shorter duration of hospitalization. There was no difference in 28-day mortality, however, for patients who were not receiving any respiratory support at the time of randomization. Conversely, there was a slight trend towards worse outcomes in those receiving no respiratory support (mortality 18% vs 14%). At time of writing, the pediatric portion of the RECOVERY trial is still enrolling patients.

Similarly, results from a large (140 received glucocorticoids vs. 1,666 who did not) noncontrolled retrospective cohort comparison reported decreased mortality or mechanical ventilation (odds ratio 0.23; 95% CI, 0.08-0.70) in those with high CRP values (20 mg/dL or higher) receiving glucocorticoids within 48 hours of hospital admission [144] . However, mortality or mechanical ventilation was increased in those receiving glucocorticoids if the CRP was less than 10 mg/dL (odds ratio, 2.64; 95% CI, 1.39-5.03).

Finally, it is worth noting that some centers are reporting their experience with a combined tocilizumab plus corticosteroid strategy for severe/critical COVID-19 patients [145, 146] . Current evidence is too limited to determine whether this strategy is truly safe, effective, and/or applicable to pediatric COVID-19 patients.

Thus, there is evolving evidence to support benefit of corticosteroid treatment for critically ill adult patients with COVID-19. The degree to which findings from these studies are applicable to children with severe or critical COVID-19 is not clear at this point. Despite this uncertainty, glucocorticoid therapy could be considered in select clinical scenarios based on individualized riskbenefit assessment. Scenario-specific guidance follows. We have not provided specific dosing A c c e p t e d M a n u s c r i p t 20 recommendations beyond the below guidance statements due to the lack of COVID-19 specific evidence for dosing at present.

Guidance Statement:

Glucocorticoid therapy is not currently indicated for outpatients or hospitalized patients with mild or moderate COVID-19.

Based on currently available data, most SARS-CoV-2 infected children, even those with mild or moderate disease, will recover with supportive care. Based on SARS and MERS studies in which glucocorticoid recipients had delayed viral clearance [137, 147] , administration of glucocorticoids may attenuate the immune response needed to clear viral infection. In addition, no evidence exists that glucocorticoid therapy prevents progression from mild/moderate to severe COVID-19.

Therefore, the panel recommends against the use of glucocorticoids in children without symptoms or who have only mild or moderate disease.

Glucocorticoid therapy may be considered for pediatric patients with critical COVID-19 with preference for use in the setting of clinical trials, if available.

As described above with regard to IL-6 and IL-1 inhibition, current evidence suggests that excessive Diagnosis with COVID-19 does not preclude use of steroids when they are otherwise indicated (for example, in asthma or catecholamine-refractory shock).

Glucocorticoid therapy offers benefit in the treatment of many pediatric conditions such as asthma exacerbation or flares in inflammatory bowel disease [148, 149] . In the critical care setting, there is limited pediatric data surrounding the efficacy of glucocorticoids in septic shock, with published studies containing small numbers of children [150] [151] [152] . A recent meta-analysis evaluating the efficacy of glucocorticoids in sepsis included 42 published RCTs of which 3 enrolled only children and 1 enrolled both adults and children [153] . Pooled analysis showed that use of glucocorticoids may decrease both short-term and long-term mortality, though any effect is likely small. A recent Cochrane review included 61 RCTs, though only 8 trials included children [154] . The authors found a small reduction in 28-day mortality in the pooled analysis, though there was significant heterogeneity across trials.

There is no high-quality pediatric data to support the routine use of glucocorticoid therapy for the treatment of sepsis without shock or shock that is responsive to fluid resuscitation or vasopressors. However, if a child with COVID-19 develops circulatory shock and remains hypotensive despite fluid resuscitation and titration of vasoactive drugs, use of glucocorticoids can be considered for treatment of critical-illness related corticosteroid insufficiency. This condition is characterized by dysregulated systemic inflammation resulting from inadequate glucocorticoid-mediated antiinflammatory activity relative to the severity of the patient's critical illness [155] . Hydrocortisone is the synthetic form of cortisol, and there is significant experience with its use in the treatment of circulatory shock. Published dosing regimens in this setting are based dosing ranges for the use of hydrocortisone in pediatric adrenal insufficiency [152, 156] . Prior guidelines for critically ill adults with COVID-19 have also addressed this topic [157, 158] .

Short-term use of glucocorticoids is associated with significant adverse effects, including hypertension and fluid retention, hyperglycemia, adrenal suppression, gastritis and gastrointestinal bleeding, posterior reversible encephalopathy syndrome [159] , and psychosis [160, 161] . We recommend routine screening for electrolyte abnormalities, hyperglycemia and hypertension in hospitalized children receiving steroids. These studies are often part of routine care. After the 2003 SARS pandemic, there were reports of avascular necrosis after treatment with glucocorticoids [162- A c c e p t e d M a n u s c r i p t 22 166 ]. In symptomatic patients, or those at increased risk of avascular necrosis, screening with plain radiographs or MRI should be considered.

Glucocorticoid therapy is also associated with immunosuppression and potentially increases the risk of secondary infection. In one recent meta-analysis of the use of glucocorticoids as adjunctive treatment for influenza, adults treated with glucocorticoids had increased odds of hospital-acquired infection, though the overall quality of evidence was low [167] . In addition, several reports of adult COVID-19 patients indicate risk for invasive pulmonary aspergillosis [168, 169] .

Whether this risk is similarly present in children with COVID-19 remains unclear. Regardless, monitoring for secondary infection should occur for all patients receiving glucocorticoids.

Monitoring for drug-drug interactions is essential with glucocorticoid use. Glucocorticoids are metabolized through cytochrome P450, 3A4, one of the more common hepatic isoenzymes. If this isoenzyme is inhibited by another agent (e.g. macrolide, protease inhibitor), significantly increased glucocorticoid exposure can result. Alternatively, glucocorticoid exposure can also be significantly reduced by an inducer of CYP 3A4 such as rifampin requiring increased dosing to obtain the same effect [170] .

Guidance statement:

While there exists a theoretical rationale for the use of JAK inhibitors in severe COVID-19, the exact clinical impact of these drugs is difficult to predict, and it is unclear whether treatment with these agents would prove beneficial or harmful. Additionally, there are very little data supporting safety or efficacy in the use of JAK inhibitors for management of COVID-19. Moreover, data from use in other settings suggests the potential for impaired viral clearance as evidenced by herpesvirus reactivations on JAK inhibitor therapy [171] . Therefore, currently, we recommend against the use of these drugs for children with COVID-19 outside of clinical trials. Mechanism and current uses: The Janus kinases (JAKs) are a family of four tyrosine kinases (JAK1, JAK2, JAK3, and TYK2) that serve as intracellular signal transducers [172] . Following the binding of cytokines to types 1 and 2 cytokine receptors on the cell surface, JAKs initiate a cascade of intracellular signaling that leads to activation or suppression of gene transcription. More than 50 cytokines signal via the JAK/STAT pathway to coordinate hematopoiesis, induce inflammation and control the immune response [172] . Cytokine receptor subunits bind specific JAKs, although some bind more than one. Complete receptors are thus associated with a pair of JAKs, and individual cytokines signal through a variety of JAK combinations.

Given the key role played by JAKs in hematopoiesis and immune signaling, these enzymes are an important target for pharmacologic inhibition. Several oral small molecule JAK inhibitors have been recently developed, and these drugs have efficacy in treating a number of neoplastic and inflammatory conditions [173] . Emerging pediatric uses for these drugs include treatment of juvenile idiopathic arthritis [174] , psoriasis [175] , interferonopathies [175] , and graft versus host disease [176, 177] . In addition to the above conditions, JAK inhibitors are also increasingly studied in the setting of CSS such as HLH and MAS [178] [179] [180] [181] . In a small open-label series of five adults with secondary HLH, ruxolitinib initiation was temporally associated with improvement in cytopenias and declines in both ferritin and soluble-IL-2 receptor (sIL2R) [178] .

In vitro and animal data: Data summarizing key cytokines and pathways relevant for JAK inhibitors are discussed in other sections.

Human data: A few small studies have evaluated the utility of JAK inhibitor therapy for COVID-19 in adults have recently been published. A single-blinded, randomized controlled trial of 43 adults with severe COVID-19 showed that ruxolitinib did not significantly enhance clinical improvement compared to placebo [182] . Ruxolitinib-treated patients in this study did show more rapid radiographic and more rapid recovery from lymphopenia as well as decrease in peripheral blood cytokine expression.

In a small cohort study, fifteen adult patients hospitalized with COVID-19 (with 9 requiring ICU care and 4 requiring mechanical ventilation) received baracitinib treatment [183] . Twelve of the fifteen patients survived though no comparator group was provided in this analysis. Finally, in a multicenter study from Italy, 113 baracitinib-treated patients with moderate COVID-19 were compared to 79 historical controls that did not receive baracitinib [184] . ICU admission and mortality A c c e p t e d M a n u s c r i p t 24 at 2 weeks post-enrollment was decreased in the baracitinib versus control groups (ICU: 0.88% vs.

17.9%, p=0.02; Mortality: 0% vs. 6.4%, p=0.01).

Thus, clinical evidence is lacking to strongly support the use of JAK inhibitors for COVID-19 patients at this point. However, large prospective studies assessing both efficacy and adverse effects are needed prior to consideration for use of these medications in children.

When studied for treatment of rheumatoid arthritis, JAK inhibitors have been shown to have a similar increased risk of infection compared to placebo as with biologic agents (e.g. adalimumab).

However, increased risk of primary or reactivation of herpes simplex and varicella zoster virus infections has been specifically noted for JAK inhibitors [185, 186] . These agents have also been associated with anemia, lymphopenia or neutropenia (and thrombocytopenia in patients with myelofibrosis treated with ruxolitinib), and with elevated cholesterol and abnormal liver function tests [187] . These effects are generally mild but occasionally require drug dosage decrease, and in cases of moderate to severe lymphopenia or neutropenia, discontinuation of the drug. Indeed, a two-patient case series recently reported demonstrated adverse effects of ruxolitinib therapy for COVID-19, including anemia, thrombocytopenia, soft tissue infection, and herpes labialis [188] .

Of note, baracitinib has a black box warning for potential increased risk of thrombosis which merits close attention in light of high reported incidence of thromboembolism in hospitalized COVID-19 patients [189, 190] .

Finally, several JAK inhibitor agents (fedratinib, ruxolitinib and tofacitinib, specifically) are considered strong substrates of CYP3A4, and therefore put patients at risk for multiple clinically relevant drug interactions including with -azole antifungals [191] . Of particular interest, care providers should use extreme caution in patient receiving potent CYP3A4 inhibitors (-azole antifungals) and potent inducers of 3A4 (phenobarbital and phenytoin) as this combination will likely cause subtherapeutic response or increase risks for adverse event with even single dose therapy. [192] . While the passive transfer of polyclonal antibodies via convalescent plasma may be of benefit, no SARS-CoV-2-specific monoclonal antibody therapies have yet been clinically tested.

With respect to coronaviruses, use of CP was trialed in MERS and more extensively in SARS [193] [194] [195] . While the SARS case series suggested possible benefit from CP for patients (especially those treated before day 14 of illness), the true efficacy of this approach remains difficult to ascertain due to lack of control groups, study biases, and use of concomitant therapeutics, all of which confound the interpretations; nonetheless, two meta-analyses of the published case series did not reveal significant harm [138, 196] . With respect to SARS-CoV-2, plasma collected from patients in the convalescent phase of infection has been used as an empirical treatment in small numbers of patients with severe COVID-19 disease, with some laboratory improvements and disease mitigation observed [197] [198] [199] [200] [201] . A small randomized controlled trial has also been conducted, although, was stopped early due to challenges with enrollment [202] .

Human data: Two studies demonstrate that while the patterns of development of IgM and IgG can differ among different individuals, nearly all COVID-19 patients eventually do develop appreciable antibody titers [203, 204] . These and other studies collectively show that the titers of SARS-CoV-2specific antibodies appear to be stable over the few ensuing weeks and that the majority of the neutralizing antibodies are directed against the spike protein, and specifically the portions of this protein that are responsible for the binding of virus to the ACE2 receptor. As such, these studies A c c e p t e d M a n u s c r i p t 26 suggest that the CP of many COVID-19 patients may contain sufficient quantities of neutralizing antibodies for therapeutic utility.

There have been several case reports and series examining passive transfer of CP to COVIDafflicted adult patients with moderate to critical disease [197-201, 205, 206] . Not all of these case series reported the titers of SARS-CoV-2 antibodies in the transferred plasma. Most of these case series reported that subsequent to CP, most patients displayed stabilization or improvement of disease, as evidenced by resolution of fever, decreases in C-reactive protein and inflammatory cytokine levels, and improved radiographic findings; in some cases these improvements resulted in the extubation of mechanically ventilated patients and weaning from ECMO support. However, in one case series, in which patients were treated with CP at a median time of 21.5 days from detection of SARS-CoV-2, 5 of 6 patients eventually died [206] , even though the virus could no longer be detected. While the numbers of patients reported to have been treated with CP to date are too small to draw any definitive conclusions, similarly to the use of CP in SARS-CoV-1 [193] , these reports do suggest that if CP is to be effective, it may need to be used earlier in the course of disease. The largest case series to date, including 5000 hospitalized adults at several centers across the United States, demonstrated only 36 severe adverse events, with only 2 of these severe adverse events judged to be definitively related to the infusion of convalescent plasma (Joyner et al JCI). This study was not designed to evaluate the efficacy of convalescent plasma.

As of July 2020, a single randomized controlled trial has evaluated convalescent plasma for SARS-CoV-2 [202] . This trial enrolled 103 patients with severe or life-threatening COVID-19 but was discontinued early due to poor accrual and thus was not powered sufficiently to answer questions of efficacy. There was no clinically significant difference found in the primary measure of time to clinical improvement. Similarly, no significant difference was identified in 28-day mortality or time to discharge. However, convalescent plasma infusion was associated with a statistically significant negative conversion rate of viral RT-PCR at 72 hours post infusion.

There is a single case report of the use of convalescent plasma for a pediatric patient [207] . Potential Risks: There are a number of potential risks associated with the use of convalescent plasma therapy, including those that may result from the transfer of immunoglobulins, and those that may ensue from transfusion of human blood products. As noted above, current reports indicate that CP-infusion is generally safe. Therefore, we focus below on immunoglobulin-dependent risks including ADE and exacerbation of deleterious immune responses, as well as the potential for inhibiting the development of effective humoral immunity.

ADE is a phenomenon in which complement pre-existing (or transferred) virus-specific antibodies could increase the entry of virus into cells expressing Fc receptors; ADE has been demonstrated to occur in a variety of viruses in vitro and in animal studies, and postulated to occur with coronaviruses [208] . ADE is believed to occur with sub-neutralizing or non-neutralizing antibodies and higher viral titers. Notably, ADE has not been demonstrated in the passive transfer of convalescent plasma in patients infected with SARS-CoV-1 and MERS. Yet, the risk of ADE still remains a concern since some patients who have recovered from mild COVID-19 may have delayed development of significant titers of neutralizing antibody titers against SARS-CoV-2, and since not all current convalescent plasma protocols mandate the use of cutoffs for neutralizing antibody titers [192, 209] . In addition to ADE, transfer of virus-specific antibodies may also exacerbate the inflammatory response and lead to further lung injury; this was demonstrated in vitro and in a SARS-CoV-1 macaque infection model [210] . Another theoretical concern is that use of exogenous immunoglobulins may inhibit endogenous development of adequate titers of high affinity antibodies that could protect the patient from re-challenge with the same virus, as has been demonstrated with respiratory syncytial virus [211, 212] .

In addition to the antibody-mediated concerns, there are risks associated with transfer of human blood products. These include transmission of infectious pathogens (SARS-CoV-2 and other viruses, as well as parasites such as Babesia spp. or Trypanosoma cruzi), and transfusion-related reactions including anaphylaxis, hemolysis, or transfusion-related acute lung injury (TRALI) or transfusion related acute cardiac overload (TACO) [213] . While passive immunotherapy protocols all include measures to minimize the possibility of such harm, some cannot be predicted or prevented, thus necessitating close monitoring in the days to weeks following therapy. 

We do not currently recommend use of IVIG for treatment of acute COVID-19 in pediatric patients with the exception of specific clinical scenarios in which IVIG is typically used. Importantly, our recommendations do not apply to the use of IVIG in the treatment of MIS-C.

Studies to suggest a benefit for IVIG treatment in COVID-19 are not available. Therefore, IVIG is not indicated in the majority of pediatric cases. A recent study, however, has shown that lots available from the USA and other parts of the world may variably contain antibodies to SARS-CoV-2.

Whether these are neutralizing antibodies or are clinically insignificant is difficult to discern at this time and future clinical trials are needed to prove any potential benefit for their use in patients with COVID-19 [214] . Mechanism and current uses: Immunoglobulin (IG) for intravenous (IV) administration, commonly referred to as IVIG, although licensed in the US as IGIV, contains pooled immunoglobulin G (IgG) from the plasma of thousands of blood donors and contains more than 95% unmodified IgG, and various amounts of IgA depending on the formulation. IVIG is an immunomodulating agent that produces effects on many components of the innate and adaptive immune system including the following: inhibition of complement activation, saturation of Fc receptors on macrophages [215] and suppression of inflammatory mediators [216] . Specific humoral effects include inhibition of B-cell differentiation, induction of B-cell apoptosis, down-regulation of specific auto-reactive B-cells, and overall inhibition of antibody production. IVIG also induces the expansion of regulatory T cells (Tregs) and downregulates the expansion of Th17 cells [217] .

Currently, the FDA has approved the use of IVIG in different clinical conditions: replacement of IgG in primary and secondary immunodeficiency disorders; prevention of coronary aneurysms in Kawasaki disease; chronic inflammatory demyelinating polyneuropathies and multifocal motor neuropathy to improve neuromuscular disability; and to improve platelet counts in immunemediated thrombocytopenia [218] .IVIG has also been used as an adjunct treatment in HLH along with other specific anti-cytokine therapy [102, 219] .

In vitro and animal data: Assessment of the role of IVIG in SARS, MERS, or COVID-19 has not been evaluated through in vitro or animal model studies.

Human data: In the SARS-CoV-1 outbreak, thrombocytopenia was reported to occur in up to 55% of patients and was identified as a significant risk factor for mortality. The etiology of this thrombocytopenia was likely multifactorial, but may have been immune complex mediated [220] .

While no data is available regarding IVIG use in the setting of SARS-CoV-1 or MERS infection, several other viral infections (e.g., HIV, hepatitis C, parvovirus B19 and Zika virus) may be associated with secondary ITP and IVIG has been used as therapy in these settings. Among 5 patients with severe thrombocytopenia with Zika virus who received IVIG, the median platelet count increase was 112 ×10 9 /L, in contrast to the median increase of 8.5 ×10 9 /L in the 4 patients who received platelet transfusions [221] .

Since severe thrombocytopenia may be associated with increased mortality in COVID-19 disease [12, 222] , there may be a role for IVIG in treatment regimens for pediatric COVID-19 patients with thrombocytopenia. However, a causal relationship between thrombocytopenia and COVID-19-A c c e p t e d M a n u s c r i p t 30 associated mortality is not established and the mechanisms for COVID-associated thrombocytopenia are not known. Therefore, benefit of IVIG in the care of pediatric COVID-19 patients is not defined.

Given the nature of the product and its source, immediate hypersensitivity and infusion related reactions such as headaches, flushing of the face, malaise, chest tightness, fever, chills, myalgia, dyspnea, nausea, vomiting, diarrhea, change in blood pressure, and tachycardia may occur and may be more likely in IgA-deficient patients who are receiving products that contain IgA [218] .

Most of these reactions can be managed or resolved by appropriate premedication regimens and slowing rates of infusion. Renal injury may be more likely in those with preexisting renal disease, volume depletion, sepsis and concomitant nephrotoxic drug usage, and may also be specific to the IVIG product used. Other specific considerations should include thromboembolism and volume considerations with administration of IVIG, especially in patients with underlying cardiac disease.

Dosing recommendations for IVIG vary by indication. Therefore, we do not provide extensive dosing guidance here. In pediatric patients with macrophage activation syndrome-related CSS an IVIG dose of 2 g/kg has been used [223] . A recent publication reported IVIG dosing of 0.3-0.5 mg/kg x5 days in a case series of COVID-19 patients [224] . There are three types of interferons: type I, type II and type III. Type I IFN includes IFN- and -, Type II interferon is IFN- and Type III includes IFN-. While type I interferon is produced by all cell types, plasmacytoid dendritic cells, fibroblasts, and monocytes are among the main sources [225] . Type I IFN secretion is induced by any cell type upon encountering viral signatures. In addition, type I IFNs enhances the clearance of virally infected cells by cytotoxic CD8 T cells by increasing the expression of MHC class I. Other effects that further enhance antiviral responses include the activation of dendritic cells, macrophages and NK cells, and the induction of the production of chemokines such as CXCL9, -10, and -11 [225] . Unlike the ubiquitously expressed IFN- receptor, the IFN- receptor is expressed in epithelial cells and a subset of immune cells, including neutrophils [226, 227] . Based on its receptor expression, it is thought that type III IFN responses have critical roles in epithelial and mucosal antiviral immunity [226, 227] . When used in patients, IFN- due to limited expression of its receptor in the immune compartment results in less systemic side effects than type I IFN therapy [228] .

Type I IFN has been extensively used in the management of Hepatitis B and C infections. Due to side effects, modest efficacy, and the advent of effective antivirals, the use of IFN- has decreased in the management of hepatitis B [229, 230] . Additionally, IFN- has also shown clinical efficacy similar to Type 1 IFN in the management of hepatitis C [228] .

In vitro and animal data: In vitro studies have shown IFN- and - have antiviral activity. However, IFN- has a more potent coronavirus suppression activity than IFN-α *11 -13] . Studies in murine models have shown that IFN- in combination with antivirals improves pulmonary function but does not reduce viral replication or severe lung pathology [14] . Similar reduction in mortality was also noted in non-human primates treated with IFN-β1b following MERS-CoV infection [15] .

Though there are no corresponding coronavirus murine model studies with IFN-, murine models of influenza A virus (IAV) infection showed promising results. IFN-λ treatment resulted in enhanced epithelial barrier function and suppressed initial viral spread without activating the systemic effects seen with IFN-α therapy *16, 17+. Importantly, while IFN-λ treatment of IAV-infected mice lowered the viral load and protected from disease, treatment with IFN-α decreased the viral load but exacerbated disease [16] .

Human data: It was recently suggested that one component of SARS-CoV-2-related immunopathology is insufficient robust type I, II or III IFN response [54] [55] [56] [57] 231] . This finding along with the known antiviral properties of both type I and type III IFN form the basis of its use in SARS-A c c e p t e d M a n u s c r i p t 32 CoV-2 [232] . Currently, there is only one published clinical trial of IFN therapy in COVID-19 [233] . In this multicenter, open-label randomized study in Hong Kong, 41 control subjects received lopinavirritonavir and 86 adult subjects received intervention therapy with lopinavir-ritonavir as well as oral ribavirin and subcutaneous IFN-β1b. Subjects were comparable with regard to clinical and laboratory characteristics and underwent treatment initiation a median of 5 days after symptom onset.

Subjects in the group receiving the addition of ribavirin and IFN-β1b to lopinavir-ritonavir had shorter time to complete symptom resolution and shorter time to negative nasopharyngeal swab compared to the control group. Further studies of interferon-β are ongoing, including with administration via inhalation which may decrease systemic side effects (NCT04385095).

Therapy with Type I or Type III IFN is associated with a variety of common adverse effects including fatigue, anorexia, nausea, diarrhea, alopecia, fever, rigors, headache, and myalgia [228, 234] . Additionally, neuropsychiatric events including depression are reported [235] . Finally, neutropenia and anemia are also reported.

Additionally, there is theoretical risk for worsening disease with the use of interferon therapy. As morbidity due to COVID-19 appears to be due in large part to hyperinflammation, potential exists for interferon therapy to result in enhanced inflammation and thereby lead to worsening of the CSS [120] . Further, there is a concern that Type I and III IFNs may impair successful antibacterial immune responses and thereby contribute to increased susceptibility to secondary bacterial infections [236, 237] .

As we do not suggest use of interferon therapy in pediatric COVID-19 patients, potential dosing and other considerations are not provided.

In addition to the above described immunomodulatory therapies, a number of other agents and immune pathways are being evaluated for treatment of COVID-19. These include immunosuppressive medications traditionally used in the setting of solid organ or hematopoietic cell transplantation, such as tacrolimus (NCT04341038), sirolimus (NCT04341675, NCT04371640), and CTLA4-Fc fusion molecules. The anti-IFN-γ antibody, emapalumab, has recently been demonstrated to have efficacy in the treatment of pediatric primary HLH [238] and is also being evaluated in the treatment of COVID-19 (NCT04324021).

A c c e p t e d M a n u s c r i p t 33

Current data demonstrate that the vast majority of pediatric patients with acute COVID-19 recover from their initial illness without significant morbidity or mortality. However, a subset of pediatric patients progresses to severe or critical acute COVID-19 and may benefit from the use of immunomodulatory therapies that are currently being evaluated in adult COVID-19 patients. Given the paucity of randomized controlled trials of immunomodulatory therapies for COVID-19 in pediatric patients, we have provided the above guidance to support pediatric subspecialists caring for severely and critically ill pediatric COVID-19 patients. Randomized controlled trials of immunomodulatory therapies for pediatric acute COVID-19 are needed.

A c c e p t e d M a n u s c r i p t 34 M a n u s c r i p t M a n u s c r i p t M a n u s c r i p t

Early Transmission Dynamics in Wuhan, China, of Novel Coronavirus-Infected Pneumonia

Detection of Covid-19 in Children in Early

Coronavirus Disease 2019 in Children -United States

Co-infection and Other Clinical Characteristics of COVID-19 in Children

Characteristics and Outcomes of Children With Coronavirus Disease 2019 (COVID-19) Infection Admitted to US and Canadian Pediatric Intensive Care Units

Severe Outcomes Among Patients with Coronavirus Disease 2019 (COVID-19) -United States

Comorbidity and its impact on 1590 patients with Covid-19 in China: A Nationwide Analysis

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection in Children and Adolescents: A Systematic Review

A Novel Coronavirus from Patients with Pneumonia in China

Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China

Clinical and immunological features of severe and moderate coronavirus disease 2019

Clinical characteristics of refractory COVID-19 pneumonia in Wuhan, China

Clinical Characteristics of 138 Hospitalized Patients With 2019 Novel Coronavirus-Infected Pneumonia in Wuhan, China

Association of Cardiac Injury With Mortality in Hospitalized Patients With COVID-19 in

Cardiac Involvement in a Patient With Coronavirus Disease 2019 (COVID-19)

Into the eye of the cytokine storm

Pathogenic human coronavirus infections: causes and consequences of cytokine storm and immunopathology

An interferon-gamma-related cytokine storm in SARS patients

Analysis of serum cytokines in patients with severe acute respiratory syndrome

Lung pathology of fatal severe acute respiratory syndrome

Multiple organ infection and the pathogenesis of SARS

Fatal outcome of human influenza A (H5N1) is associated with high viral load and hypercytokinemia

Profiles of acute cytokine and antibody responses in patients infected with avian influenza A H7N9

Role of host immune response and viral load in the differential outcome of pandemic H1N1 (2009) influenza virus infection in Indian patients

Cytokine response patterns in severe pandemic 2009 H1N1 and seasonal influenza among hospitalized adults

Whole-Exome Sequencing Reveals Mutations in Genes Linked to Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome in Fatal Cases of H1N1 Influenza

An Acute Immune Response to Middle East Respiratory Syndrome Coronavirus Replication Contributes to Viral Pathogenicity

Clinical course and outcomes of critically ill patients with Middle East respiratory syndrome coronavirus infection

Immunohistochemical, and Ultrastructural Findings of a Fatal Case of Middle East Respiratory Syndrome Coronavirus Infection in the United Arab Emirates

Macrophage activation syndrome in the era of biologic therapy

A banner year for immunotherapy and targeted therapy

Future Prospects of Biologic Therapies for Immunologic Diseases

Cytokine Release Syndrome with Chimeric Antigen Receptor T Cell Therapy

An outbreak of severe Kawasaki-like disease at the Italian epicentre of the SARS-CoV-2 epidemic: an observational cohort study

COVID-19 and Kawasaki Disease: Novel Virus and Novel Case

Hyperinflammatory shock in children during COVID-19 pandemic

Rapid risk assessment: Paediatric inflammatory multisystem syndrome and SARS-CoV-2 infection in children

COVID-19 Associated Pediatric Multi-System Inflammatory Syndrome

Multisystem Inflammatory Syndrome in Children (MIS-C) Associated with Coronavirus Disease 2019 (COVID-19)

First case of COVID-19 in a patient with multiple myeloma successfully treated with tocilizumab

Tocilizumab, an anti-IL6 receptor antibody, to treat Covid-19-related respiratory failure: a case report

Tocilizumab treatment in COVID-19: A single center experience

Rapid and Severe Covid-19 Pneumonia with Severe Acute Chest Syndrome in a Sickle Cell Patient Successfully Treated with Tocilizumab

Off-label Use of Tocilizumab in Patients with SARS-CoV-2 Infection

Multicenter initial guidance on use of antivirals for children with COVID-19/SARS-CoV-2

COVID-19 in children and adolescents in Europe: a multinational, multicentre cohort study

Clinical Manifestations and Outcomes of Critically Ill Children and Adolescents with COVID-19 in New York City

Post-mortem examination of COVID19 patients reveals diffuse alveolar damage with severe capillary congestion and variegated findings of lungs and other organs suggesting vascular dysfunction

Autopsy Findings and Venous Thromboembolism in Patients With COVID-19

Hematologic, biochemical and immune biomarker abnormalities associated with severe illness and mortality in coronavirus disease 2019 (COVID-19): a meta-analysis

COVID-19 and its implications for thrombosis and anticoagulation

Plasma IP-10 and MCP-3 levels are highly associated with disease severity and predict the progression of COVID-19

Immune cell profiling of COVID-19 patients in the recovery stage by single-cell sequencing

Impaired type I interferon activity and inflammatory responses in severe COVID-19 patients

Type I IFN immunoprofiling in COVID-19 patients

Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19

Dysregulated Type I Interferon and Inflammatory Monocyte-Macrophage Responses Cause Lethal Pneumonia in SARS-CoV-Infected Mice

Targeting the inflammatory cascade with anakinra in moderate to severe COVID-19 pneumonia: case series

Interleukin-1 blockade with high-dose anakinra in patients with COVID-19, acute respiratory distress syndrome, and hyperinflammation: a retrospective cohort study

Favorable Anakinra Responses in Severe Covid-19 Patients with Secondary Hemophagocytic Lymphohistiocytosis

Tocilizumab for the treatment of severe coronavirus disease 2019

Interleukin-6: A Masterplayer in the Cytokine Network

Impaired immune and acute-phase responses in interleukin-6-deficient mice

Late interleukin-6 escalates T follicular helper cell responses and controls a chronic viral infection

HBV replication is significantly reduced by IL-6

Interleukin-6 limits influenza-induced inflammation and protects against fatal lung pathology

Delayed induction of proinflammatory cytokines and suppression of innate antiviral response by the novel Middle East respiratory syndrome coronavirus: implications for pathogenesis and treatment

Active replication of Middle East respiratory syndrome coronavirus and aberrant induction of inflammatory cytokines and chemokines in human macrophages: implications for pathogenesis

Up-regulation of IL-6 and TNF-alpha induced by SARS-coronavirus spike protein in murine macrophages via NF-kappaB pathway

Nucleocapsid protein of SARS-CoV activates interleukin-6 expression through cellular transcription factor NF-kappaB

Lack of innate interferon responses during SARS coronavirus infection in a vaccination and reinfection ferret model

Detectable serum SARS-CoV-2 viral load (RNAaemia) is closely correlated with drastically elevated interleukin 6 (IL-6) level in critically ill COVID-19 patients

Clinical predictors of mortality due to COVID-19 based on an analysis of data of 150 patients from Wuhan, China

Characteristics of pediatric SARS-CoV-2 infection and potential evidence for persistent fecal viral shedding

Tocilizumab for treatment of mechanically ventilated patients with COVID-19

Tocilizumab in patients with severe COVID-19: a retrospective cohort study

Tocilizumab Treatment for Cytokine Release Syndrome in Hospitalized COVID-19 Patients: Survival and Clinical Outcomes

Pilot prospective open, single-arm multicentre study on offlabel use of tocilizumab in patients with severe COVID-19

Efficacy and safety of tocilizumab in severe COVID-19 patients: a single-centre retrospective cohort study

Effective treatment of severe COVID-19 patients with tocilizumab

Tocilizumab for the treatment of severe COVID-19 pneumonia with hyperinflammatory syndrome and acute respiratory failure: A single center study of 100 patients in

Pneumatosis Intestinalis and Intestinal Perforation in a

Transaminase Levels and Hepatic Events During Tocilizumab Treatment: Pooled Analysis of Long-Term Clinical Trial Safety Data in Rheumatoid Arthritis

Letter to the Editor: Acute hypertriglyceridemia in patients with COVID-19 receiving tocilizumab

Anakinra for severe forms of COVID-19: a cohort study

Canakinumab in a subgroup of patients with COVID-19

Critical regulation of early Th17 cell differentiation by interleukin-1 signaling

Interleukin (IL) 1beta induction of IL-6 is mediated by a novel phosphatidylinositol 3-kinase-dependent AKT/IkappaB kinase alpha pathway targeting activator protein-1

Anakinra Therapy for Non-cancer Inflammatory Diseases

Rilonacept and canakinumab

European Group Of Clinical I. Long-term safety and maintenance of clinical improvement following treatment with anakinra (recombinant human interleukin-1 receptor antagonist) in patients with rheumatoid arthritis: extension phase of a randomized, double-blind, placebo-controlled trial

A multicentre, double blind, randomised, placebo controlled trial of anakinra (Kineret), a recombinant interleukin 1 receptor antagonist, in patients with rheumatoid arthritis treated with background methotrexate

Randomized, double-blind, placebo-controlled trial of the efficacy and safety of rilonacept in the treatment of systemic juvenile idiopathic arthritis

Efficacy and safety of rilonacept

Trap) in patients with cryopyrin-associated periodic syndromes: results from two sequential placebo-controlled studies

Sustained remission of symptoms and improved health-related quality of life in patients with cryopyrin-associated periodic syndrome treated with canakinumab: results of a double-blind placebo-controlled randomized withdrawal study

Canakinumab for the Treatment of Autoinflammatory Recurrent Fever Syndromes

Two randomized trials of canakinumab in systemic juvenile idiopathic arthritis

Interleukin-1 Receptor Blockade Is Associated With Reduced Mortality in Sepsis Patients With Features of Macrophage Activation Syndrome: Reanalysis of a Prior Phase III Trial

Successful treatment of severe paediatric rheumatic disease-associated macrophage activation syndrome with interleukin-1 inhibition following conventional immunosuppressive therapy: case series with 12 patients

Benefit of Anakinra in Treating Pediatric Secondary Hemophagocytic Lymphohistiocytosis

Therapeutic role of anakinra, an interleukin-1 receptor antagonist, in the management of secondary hemophagocytic lymphohistiocytosis/sepsis/multiple organ dysfunction/macrophage activating syndrome in critically ill children*

Factors affecting the measurement of cytokines in biological fluids: implications for their clinical measurement

Severe Acute Respiratory Syndrome Coronavirus Viroporin 3a Activates the NLRP3 Inflammasome

Severe acute respiratory syndrome coronavirus E protein transports calcium ions and activates the NLRP3 inflammasome

Severe acute respiratory syndrome coronavirus ORF3a protein activates the NLRP3 inflammasome by promoting TRAF3-dependent ubiquitination of ASC

SARS-Coronavirus Open Reading Frame-8b triggers intracellular stress pathways and activates NLRP3 inflammasomes

Clinical characteristics and mechanism of liver injury in patients with severe acute respiratory syndrome

Plasma inflammatory cytokines and chemokines in severe acute respiratory syndrome

Inflammatory cytokine profile in children with severe acute respiratory syndrome

Expression of elevated levels of pro-inflammatory cytokines in SARS-CoV-infected ACE2+ cells in SARS patients: relation to the acute lung injury and pathogenesis of SARS

Interleukin-1 blockade with high-dose anakinra in patients with COVID-19, acute respiratory distress syndrome, and hyperinflammation: a retrospective cohort study

Predictors of Effectiveness of Anakinra in Systemic Juvenile Idiopathic Arthritis

Anakinra treatment in macrophage activation syndrome: a single center experience and systemic review of literature

Risk of serious infections during rituximab, abatacept and anakinra treatments for rheumatoid arthritis: meta-analyses of randomised placebocontrolled trials

Silencing the cytokine storm: the use of intravenous anakinra in haemophagocytic lymphohistiocytosis or macrophage activation syndrome

Continuous Intravenous Anakinra Infusion to Calm the Cytokine Storm in Macrophage Activation Syndrome

Long-term safety profile of anakinra in patients with severe cryopyrin-associated periodic syndromes

Long-term surveillance of biologic therapies in systemiconset juvenile idiopathic arthritis: data from the German BIKER registry

COVID-19: consider cytokine storm syndromes and immunosuppression

On the use of corticosteroids for 2019-nCoV pneumonia

Clinical evidence does not support corticosteroid treatment for 2019-nCoV lung injury

Immune regulation by glucocorticoids

How glucocorticoid receptors modulate the activity of other transcription factors: a scope beyond tethering

Glucocorticoid and cytokine crosstalk: Feedback, feedforward, and co-regulatory interactions determine repression or resistance

Glucocorticoid modulation of cytokine signaling

Glucocorticoids in T cell apoptosis and function

A Major Outbreak of Severe Acute Respiratory Syndrome in Hong Kong

Clinical features and short-term outcomes of 144 patients with SARS in the greater Toronto area

Acute respiratory distress syndrome in critically ill patients with severe acute respiratory syndrome

Clinical progression and viral load in a community outbreak of coronavirus-associated SARS pneumonia: a prospective study

Outcome of coronavirus-associated severe acute respiratory syndrome using a standard treatment protocol

Severe acute respiratory syndrome: report of treatment and outcome after a major outbreak

Corticosteroid treatment of severe acute respiratory syndrome in Hong Kong

High-dose pulse versus nonpulse corticosteroid regimens in severe acute respiratory syndrome

Treatment of severe acute respiratory syndrome with glucosteroids: the Guangzhou experience

Effects of early corticosteroid treatment on plasma SARSassociated Coronavirus RNA concentrations in adult patients

SARS: systematic review of treatment effects

Clinical features of patients infected with 2019 novel coronavirus in Wuhan

Cardiovascular Implications of Fatal Outcomes of Patients With Coronavirus Disease 2019 (COVID-19)

Risk Factors Associated With Acute Respiratory Distress Syndrome and Death in Patients With Coronavirus Disease

Early Short Course Corticosteroids in Hospitalized Patients with COVID-19

Dexamethasone in Hospitalized Patients with Covid-19 -Preliminary Report

Effect of systemic glucocorticoids on mortality or mechanical ventilation in patients with COVID-19

The Combination of Tocilizumab and Methylprednisolone Along With Initial Lung Recruitment Strategy in Coronavirus Disease 2019 Patients Requiring Mechanical Ventilation: A Series of 21 Consecutive Cases

Effectiveness of corticoid pulses in patients with cytokine storm syndrome induced by SARS-CoV-2 infection

Corticosteroid Therapy for Critically Ill Patients with Middle East Respiratory Syndrome

Corticosteroids for preventing relapse following acute exacerbations of asthma

Traditional corticosteroids for induction of remission in Crohn's disease

Evaluation of Early Corticosteroid Therapy in Management of Pediatric Septic Shock in Pediatric Intensive Care Patients: A Randomized Clinical Study

Low-dose hydrocortisone in pediatric septic shock: an exploratory study in a third world setting

Surviving Sepsis Campaign International Guidelines for the Management of Septic Shock and Sepsis-Associated Organ Dysfunction in Children

Corticosteroids in Sepsis: An Updated Systematic Review and Meta-Analysis

Corticosteroids for treating sepsis in children and adults

Guidelines for the Diagnosis and Management of Critical Illness-Related Corticosteroid Insufficiency (CIRCI) in Critically Ill Patients (Part I): Society of Critical Care Medicine (SCCM) and European Society of Intensive Care Medicine (ESICM) 2017

American Academy of Pediatrics Committee on D. Preparing for pediatric emergencies: drugs to consider

Surviving Sepsis Campaign: guidelines on the management of critically ill adults with Coronavirus Disease 2019 (COVID-19)

Clinical management of severe acute respiratory infection (SARI) when COVID-19 disease is suspected

Corticosteroid therapy and severity of vasogenic edema in posterior reversible encephalopathy syndrome

Steroid-Induced Psychosis in the Pediatric Population: A New Case and Review of the Literature

Factors Associated with Psychosis among Patients with Severe Acute Respiratory Syndrome: A Case-Control Study

Avascular necrosis of bone in severe acute respiratory syndrome

Avascular osteonecrosis after treatment of SARS: a 3-year longitudinal study

Steroid therapy and the risk of osteonecrosis in SARS patients: a dose-response meta-analysis

A 12-year follow-up study of combined treatment of post-severe acute respiratory syndrome patients with femoral head necrosis

Osteonecrosis in children with severe acute respiratory syndrome

Corticosteroids as Adjunctive Therapy in the Treatment of Influenza: An Updated Cochrane Systematic Review and Meta-analysis

COVID-19-associated invasive pulmonary aspergillosis

COVID-19 associated pulmonary aspergillosis

Adrenal insufficiency, be aware of drug interactions! Endocrinol Diabetes Metab Case Rep

A systematic review and meta-analysis of infection risk with small molecule JAK inhibitors in rheumatoid arthritis

The molecular details of cytokine signaling via the JAK/STAT pathway

Back to the future: oral targeted therapy for RA and other autoimmune diseases

Tofacitinib Treatment of Refractory Systemic Juvenile Idiopathic Arthritis

JAK Inhibitors in Rheumatology: Implications for Paediatric Syndromes?

Ruxolitinib treatment for steroid refractory acute and chronic graft vs host disease in children: Clinical and immunological results

Ruxolitinib as Salvage Therapy in Steroid-Refractory Acute Graft-versus-Host Disease in Pediatric Hematopoietic Stem Cell Transplant Patients

Ruxolitinib in adult patients with secondary haemophagocytic lymphohistiocytosis: an open-label, single-centre, pilot trial

Ruxolitinib for secondary hemophagocytic lymphohistiocytosis: First case report

Ruxolitinib for treatment of refractory hemophagocytic lymphohistiocytosis

Ruxolitinib for the treatment of lymphoma-associated hemophagocytic lymphohistiocytosis: A cautionary tale

Ruxolitinib in treatment of severe coronavirus disease 2019 (COVID-19): A multicenter, single-blind, randomized controlled trial

Use of Baricitinib in Patients with Moderate and Severe COVID-19

Beneficial impact of Baricitinib in COVID-19 moderate pneumonia; multicentre study

Herpes Zoster in Patients Receiving JAK Inhibitors For Ulcerative Colitis: Mechanism, Epidemiology, Management, and Prevention

Baricitinib for COVID-19: a suitable treatment? -Authors' reply

Efficacy and safety of tofacitinib in the treatment of rheumatoid arthritis: a systematic review and meta-analysis

Side effects of ruxolitinib in patients with SARS-CoV-2 infection: two case reports

Incidence of venous thromboembolism in hospitalized patients with COVID-19

OLUMIANT: Highlights of Prescribing Information

Critical Assessment of Pharmacokinetic Drug-Drug Interaction Potential of Tofacitinib, Baricitinib and Upadacitinib, the Three Approved Janus Kinase Inhibitors for Rheumatoid Arthritis Treatment

The convalescent sera option for containing COVID-19

Use of convalescent plasma therapy in SARS patients in Hong Kong

Retrospective comparison of convalescent plasma with continuing high-dose methylprednisolone treatment in SARS patients

Challenges of convalescent plasma infusion therapy in Middle East respiratory coronavirus infection: a single centre experience

The effectiveness of convalescent plasma and hyperimmune immunoglobulin for the treatment of severe acute respiratory infections of viral etiology: a systematic review and exploratory meta-analysis

Treatment of 5 Critically Ill Patients With COVID-19 With Convalescent Plasma

Treatment With Convalescent Plasma for Critically Ill Patients With SARS-CoV-2 Infection

Effectiveness of convalescent plasma therapy in severe COVID-19 patients

Use of Convalescent Plasma Therapy in Two COVID-19 Patients with Acute Respiratory Distress Syndrome in Korea

Treatment with convalescent plasma for COVID-19 patients in Wuhan

Effect of Convalescent Plasma Therapy on Time to Clinical Improvement in Patients With Severe and Life-threatening COVID-19: A Randomized Clinical Trial

Profile of IgG and IgM antibodies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)

Antibody responses to SARS-CoV-2 in patients with COVID-19

Anti-SARS-CoV-2 virus antibody levels in convalescent plasma of six donors who have recovered from COVID-19

Effect of Convalescent Plasma Therapy on Viral Shedding and Survival in COVID-19 Patients

First case of convalescent plasma transfusion in a child with COVID-19-associated severe aplastic anemia

Molecular Mechanism for Antibody-Dependent Enhancement of Coronavirus Entry

Administration FaD

Anti-spike IgG causes severe acute lung injury by skewing macrophage responses during acute SARS-CoV infection

Passively acquired antibodies suppress humoral but not cell-mediated immunity in mice immunized with live attenuated respiratory syncytial virus vaccines

Serum and nasal-wash immunoglobulin G and A antibody response of infants and children to respiratory syncytial virus F and G glycoproteins following primary infection

Deployment of convalescent plasma for the prevention and treatment of COVID-19

Currently available intravenous immunoglobulin contains antibodies reacting against severe acute respiratory syndrome coronavirus 2 antigens

Anti-inflammatory activity of IVIG mediated through the inhibitory Fc receptor

Preparations of intravenous immunoglobulins diminish the number and proinflammatory response of CD14+CD16++ monocytes in common variable immunodeficiency (CVID) patients

Intravenous gammaglobulin inhibits encephalitogenic potential of pathogenic T cells and interferes with their trafficking to the central nervous system, implicating sphingosine-1 phosphate receptor 1-mammalian target of rapamycin axis

Update on the use of immunoglobulin in human disease: A review of evidence

Interleukin 1 Receptor Antagonist Anakinra, Intravenous Immunoglobulin, and Corticosteroids in the Management of Critically Ill Adult Patients With Hemophagocytic Lymphohistiocytosis

Thrombocytopenia in patients with severe acute respiratory syndrome (review)

Incidence and Outcome of Severe and Nonsevere Thrombocytopenia Associated With Zika Virus Infection-Puerto Rico

Thrombocytopenia is associated with severe coronavirus disease 2019 (COVID-19) infections: A meta-analysis

Macrophage Activation Syndrome

High-Dose Intravenous Immunoglobulin as a Therapeutic Option for Deteriorating Patients With Coronavirus Disease

Type I interferons in infectious disease

Interferon-lambda orchestrates innate and adaptive mucosal immune responses

COVID-19 and emerging viral infections: The case for interferon lambda

A randomized phase 2b study of peginterferon lambda-1a for the treatment of chronic HCV infection

96weeks treatment of tenofovir alafenamide vs. tenofovir disoproxil fumarate for hepatitis B virus infection

Korean Association for the Study of the L. KASL clinical practice guidelines for management of chronic hepatitis B

Comparative replication and immune activation profiles of SARS-CoV-2 and SARS-CoV in human lungs: an ex vivo study with implications for the pathogenesis of COVID-19

Weak Induction of Interferon Expression by SARS-CoV-2 Supports Clinical Trials of Interferon Lambda to Treat Early COVID-19

Triple combination of interferon beta-1b, lopinavir-ritonavir, and ribavirin in the treatment of patients admitted to hospital with COVID-19: an open-label, randomised, phase 2 trial

Premature discontinuation of interferon plus ribavirin for adverse effects: a multicentre survey in 'real world' patients with chronic hepatitis C

Neuropsychiatric adverse effects of interferon-alpha: recognition and management

Lambda Interferon Restructures the Nasal Microbiome and Increases Susceptibility to Staphylococcus aureus Superinfection

Disease-promoting effects of type I interferons in viral, bacterial, and coinfections

Emapalumab in Children with Primary Hemophagocytic Lymphohistiocytosis

The authors would like to thank Drs. Jason Newland, Kathleen Chiotos, and Mari Nakamura and the Sharing Antimicrobial Reports for Pediatric Stewardship (SHARPS) collaborative for their support in developing this document

A c c e p t e d M a n u s c r i p t 35 A c c e p t e d M a n u s c r i p t Table 1 . Suggested COVID-19 illness severity categories (modified from [45] )

No new or increased supplemental oxygen requirement.

New or increase from baseline supplemental oxygen requirement without need for new or increase in baseline non-invasive/invasive mechanical ventilation.

New or increased requirement for invasive or non-invasive mechanical ventilation, sepsis, or multi-organ failure; OR rapidly worsening clinical trajectory that does not yet meet these criteria.Comments: Non-invasive mechanical ventilation includes high-flow nasal canula, continuous positive airway pressure (CPAP), or bilevel positive airway pressure (BiPAP).A c c e p t e d M a n u s c r i p t 48 We suggest that immunomodulatory therapy only be used for pediatric patients in the setting of confirmed critical COVID-19 (SARS-CoV-2 PCR positive) with evidence of hyperinflammation (Table 4 ). In addition, pediatric COVID-19 patients with hyperinflammation whose pace of illness progression suggests imminent progression to critical COVID-19 may be considered for immunomodulatory treatment. Use of immunomodulation for pediatric COVID-19 should be performed in consultation with specialists familiar with these medications. III. WHICH IMMUNOMODULATORY AGENTS SHOULD BE CONSIDERED?  There are no immunomodulators with proven efficacy for the treatment of COVID-19 in pediatric patients as of 24 July 2020. Therefore, no guidance can be provided to support the use of one immunomodulatory therapy over another.  If immunomodulators are used in the treatment of COVID-19, patients should be monitored for adverse effects. Note: The order of discussion of each category below does not denote an order of preference. A. IL-6 inhibition IL-6 inhibition may be considered in the care of pediatric patients with critical COVID-19 with priority given to clinical trial enrollment if available. B. IL-1 inhibition IL-1 inhibition may be considered in the care of pediatric patients with critical COVID-19 with priority given to clinical trial enrollment if available. If IL-1 inhibition is used as a treatment modality for pediatric COVID-19 patients, we suggest the use of anakinra based on its safety profile and favorable pharmacokinetics.

Given their pleiotropic effects, glucocorticoids are used in a variety of inflammatory conditions and settings. As such, it is difficult to definitively support or discourage the use of glucocorticoids in all situations. Therefore, we have provided guidance for specific situations in the following section.  Glucocorticoid therapy is not currently indicated for outpatients or hospitalized patients with mild or moderate COVID-19.  Glucocorticoid therapy may be considered for pediatric patients with critical COVID-19 with preference for use in the setting of clinical trials, if available.  Diagnosis with COVID-19 does not preclude use of steroids when they are otherwise indicated (for example, in asthma or catecholamine-refractory shock).  Elevated bilirubin, GGT, and/or transaminases Renal  Decreased creatinine clearance Abbreviations: BNP, brain natriuretic peptide; CRP, C-reactive protein; CSS, cytokine storm syndrome; PT, prothrombin time; PTT, partial thromboplastin time; GGT, gamma-glutamyl transferase