key: cord-026811-6bdzut3d
authors: Jha, Ashish K.; Kumar, Ravikant; Goenka, Mahesh K.; Dayal, Vishwa M.
title: Emerging Treatment and Prevention Strategies against COVID-19: A Brief Update
date: 2020-05-16
journal: nan
DOI: 10.1055/s-0040-1712547
sha: 
doc_id: 26811
cord_uid: 6bdzut3d

Patients with novel coronavirus disease 2019 (COVID-19) are at significantly increased risk for mortality and morbidity. Current management remains supportive care, ranging from symptomatic outpatient management to full–intensive care support, including intravenous fluids, invasive, and non-invasive oxygen supplementation. In patients with septic shock, treatment with antibiotics and vasopressors are recommended to keep mean arterial pressure (MAP) ≥ 65 mm Hg and lactate < 2 mmol/L. Because of the lack of effectiveness and possible adverse effects, routine corticosteroids should be avoided unless they are indicated for another reason (exacerbation of asthma or chronic obstructive pulmonary disease [COPD], and septic shock in whom fluids and vasopressors do not restore hemodynamic stability). There is currently no sufficient evidence of efficacy of hydroxychloroquine/chloroquine, remdesivir, and other antivirals in the treatment or prevention of COVID-19. Limited evidence shows that COVID-19 convalescent plasma can be used as a treatment of COVID-19 without the occurrence of severe adverse events. Drug regulatory agencies granted an emergency-use authorization of chloroquine/hydroxychloroquine and remdesivir to treat patients when a clinical trial is not available or participation is not feasible. Chloroquine and hydroxychloroquine are associated with QT interval prolongation and life-threatening cardiac arrhythmia in patients with pre-existing cardiovascular disease. Guidelines are issued for use of convalescent plasma in patients with serious or immediately life-threatening COVID-19. Data from several ongoing randomized controlled trials will provide further evidence regarding the safety and efficacy of these drugs for the treatment of COVID-19.

The current novel coronavirus disease 2019 (COVID- 19) pandemic, caused by a novel severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2), is a rapidly spreading viral disease. Patients with COVID-19 are at significantly increased risk for mortality and morbidity. Since the first report of SARS-CoV-2 infection, it has spread to more than 210 countries around the world (2,726,776 active cases and 191,087 death [till April 24, 2020]). To date, India has recorded 23,502 active cases and 722 death (till April 24, 2020). There is currently no specific treatment of COVID-19. Current management remains supportive care, ranging from symptomatic outpatient management to full intensive care support, including intravenous fluids, invasive and noninvasive oxygen supplementation, and antibiotics. 1 The objective of this paper is to briefly review the literature and update the concept of prevention and treatment of COVID-19. We have highlighted here the potential therapeutic role of remdesivir, chloroquine/ hydroxychloroquine (HCQ), lopinavir/ritonavir, and convalescent plasma in patients with SARS-CoV-2 infection.

In the absence of a proven therapy for SARS-CoV 2, the cornerstone of therapy for patients with COVID-19 remains supportive care. to suppress the inflammatory response which may lead to acute lung injury and ARDS. In a retrospective study (n = 201), treatment with methylprednisolone was associated with a decreased risk of death (46% with steroids vs. 62% without). 2 However, the authors noted that confounding bias may exist in this observational study. Because of the lack of effectiveness and possible adverse effects, routine corticosteroids should be avoided unless they are indicated for another reason (exacerbation of asthma or COPD and septic shock in whom fluids and vasopressors do not restore hemodynamic stability). 1,3

Remdesivir is a nucleotide analogue prodrug that inhibits viral RNA polymerases. It has broad-spectrum activity against RNA viruses such as coronaviridae (e.g., SARS-CoV and Middle East respiratory syndrome coronavirus [MERS-CoV]) and filoviruses (e.g., Ebola). It has shown prophylactic and therapeutic efficacy in nonclinical models of these coronaviruses; however, there are currently only very limited data on the use of remdesivir in patients with COVID-19. In a recent multicentric study, patients with confirmed SARS-CoV-2 infection (n = 53) who had an oxygen saturation of 94% or less with or without receiving oxygen support were enrolled. Besides supportive care, patients received remdesivir, consisting of 200 mg administered intravenously on day 1, followed by 100 mg daily up to 10 days. During a median follow-up of 18 days, 68% had an improvement in oxygen-support class, including 57% patients receiving mechanical ventilation. However, interpretation of the result of this study is limited by the lack of a randomized control group, small sample size, exclusion of serious cases (creatinine clearance <30 mL/min and >five-time elevation of serum aminotransferase), variable duration of remdesivir administration, noncollection of viral load data, adverse effects, and short-term follow-up. 4 A total of 60% patients reported adverse events during follow-up. The result of a study (SIMPLE trial; unpublished) demonstrated that patients receiving a 10-day course of remdesivir achieved similar clinical improvement compared with those taking a 5-day treatment course on Day 14. The European Medicines Agency (EMA) has published recommendations on compassionate use of remdesivir for COVID-19. 5 Data from several ongoing randomized controlled trials will provide further evidence regarding the safety and efficacy of remdesivir for COVID-19.

The antimalarial and anti-inflammatory agents, chloroquine and HCQ, appear to block viral entry into cells by inhibiting glycosylation of host receptors, proteolytic processing, and endosomal acidification. These agents also have immunomodulatory effects through attenuation of cytokine production and inhibition of autophagy and lysosomal activity in host cells. 6, 7 Both drugs have in vitro activity against SARS-CoV-2, with HCQ having relatively higher potency. Early results obtained from more than 100 patients enrolled in studies conducted in the China showed the superiority of chloroquine compared with the controls in terms of reduction of exacerbation of pneumonia, duration of symptoms, and delay of viral clearance, all in the absence of severe side effects. 8 A recent open-label study of 36 patients reported improved virologic clearance with HCQ (n = 36) compared with the controls (n = 20). Addition of azithromycin to HCQ in six patients resulted in superior viral clearance (100%) compared with HCQ monotherapy (57%). 9 An uncontrolled observational study in a cohort of COVID-19 inpatients (n = 80) treated with a combination of HCQ and azithromycin showed a rapid fall of nasopharyngeal viral load (93% at day 8). 2 In a randomized parallel-group trial, COVID-19 patients (n = 31) were assigned to receive an additional 5-day HCQ (400 mg/d) treatment. Clinical recovery time was significantly shortened in the HCQ treatment group. Improvement in pneumonia was more in the HCQ treatment group (80.6%) compared with the controls (54.8%). However, the patients had mild disease. 10 In a prospective study (n = 30), patients were randomized to HCQ (400 mg/day for 5 days) plus standard of care and standard care alone groups. Virologic clearance was similar in both the groups. 11 A study of 11 patients with COVID-19 reported persistence of SARS-CoV-2 in the nasopharyngeal swab in 8 of 10 patients receiving HCQ. In a randomized, double-blinded, phase-IIb clinical trial (CloroCOVID-19 Study), preliminary findings suggest that the higher chloroquine dosage is associated with higher rate of QTc prolongation and mortality. Studies of chloroquine prophylaxis in health care workers (NCT04303507) and HCQ for postexposure prophylaxis after high-risk exposures (NCT04308668) are planned or enrolling. 12 Some studies show no benefit at all, while others show a benefit of taking HCQ/chloroquine. Some of the aforementioned clinical studies showed HCQ/chloroquine as promising agents for the treatment of mild-to-severe COVID-19. However, these trials have been criticized for their limitations, including small sample size, nonuniform study design, absence of control arm, and enrolment of less severe cases. 2, 9, 10, 13 Results from other clinical studies could not replicate these positive findings. 11, 12, 14 Therefore, there is currently no strong evidence of efficacy of HCQ or chloroquine in the treatment or prevention of COVID-19. Chinese and Italian guidelines recommend early use of HCQ or chloroquine for the treatment of COVID-19 on case-to-case basis; however, this is based on weak evidence. The Food and Drug Administration (FDA) and EMA has granted an emergency-use authorization for chloroquine and HCQ to treat patients when a clinical trial is not available or participation is not feasible. 5, 15 Indian Council of Medical Research (ICMR) recommends the use of HCQ for prophylaxis of SARS CoV-2 infection in high-risk cases. QT-prolongation and life-threatening cardiac arrhythmia is major concern in patients receiving HCQ with or without azithromycin, especially in patients with preexisting cardiovascular disease.

Lopinavir/ritonavir demonstrated in vitro activity against other corona viruses via inhibition of 3-chymotrypsin-like protease. Results of a few small case series showed clinical benefit of using with lopinavir/ritonavir in patients with COVID-19. However, an open-label randomized trial at a single hospital concluded that lopinavir/ritonavir recipients and those receiving standard care did not differ significantly in time to clinical improvement (median, 16 days), duration of intensive care unit stay, and duration of mechanical ventilation/oxygen supplementation. 16 At present, there is insufficient evidence to recommend the use of lopinavir/ritonavir for treatment of COVID-19.

Convalescent plasma from patients who have recovered from viral infections has been used as a treatment in previous virus outbreaks including SARS and Ebola virus. Convalescent plasma or immunoglobulins were used in patients with SARS whose condition continued to deteriorate despite treatment with intravenous corticosteroids. A systematic review and exploratory meta-analysis from 32 studies of SARS coronavirus infection and severe influenza showed a statistically significant reduction in the pooled odds of mortality following treatment with convalescent plasma compared with placebo (odds ratio = 0.25; 95% confidence interval [CI]:0.14-0.45; I[2] = 0%). Study showed consistent evidence for a reduction in mortality, especially when convalescent plasma is administered early after symptom onset. No serious adverse events were seen. However, studies were commonly of low or very low quality, lacked control groups, and at moderate or high risk of bias. 17 Luke et al identified eight studies involving 1,703 patients with Spanish influenza pneumonia treated with influenza-convalescent human blood products infusion, which showed a pooled absolute reduction of 21% (p < 0·001) in the overall crude case-fatality rate. Mortality rate was lower in patients who received early treatment (after <4 days of complications) compared with late treatment group (after >4 days of complications; 26 vs. 50% [pooled risk difference = 41% (CI: 29-54%)]). 18 Convalescent plasma has also been tried in treatment of COVID-19. A few small preliminary case series showed clinical improvement after treatment with convalescent plasma; however, these studies had many limitations. 19, 20 Limited evidence shows that convalescent plasma can be used as a treatment of COVID-19 without the occurrence of severe adverse events. 19 Convalescent plasma that contains antibodies to SARS-CoV-2 might suppress viremia. The patient usually develops a primary immune response by days 10 to 14, which is followed by virus clearance. Therefore, logically, it should be more effective to transfuse the convalescent plasma at the early course of disease. Studies showed lower mortality rate in whom convalescent plasma is administered early after symptom onset. 17, 18 The FDA has issued guidance for use of COVID-19 convalescent plasma in patients with serious COVID-19. About 3 to 4 weeks after a person recovers, blood can be drawn to look for the antibodies. The approach involves giving COVID-19 patients an infusion of antibody-rich plasma (single dose of 200 mL) from people who have recovered from an infection with SARS-CoV-2.

The rapidly expanding knowledge regarding SARS-CoV-2 virology provides a significant number of potential drug targets. Potential mechanisms of action of antiviral agents are (1) virus-based therapy, like monoclonal antibodies or antiviral peptides, targeting the various steps of viral machinery-like spike glycoprotein, viral enzyme inhibitors, and viral nucleic acid synthesis inhibitors, and (2) host-based therapies to potentiate the interferon response, affect host signalling pathways, or host factors utilized by SARS-CoV-2 for replication. 21 The World health Organization (WHO) has started an international multicentric clinical trial ("Solidarity"). This trial comprises of four treatment groups (remdesivir, chloroquine/hydroxychloroquine, lopinavir with ritonavir, and lopinavir with ritonavir plus interferon β-1a) against standard of care, to assess their relative effectiveness against COVID-19. 1 Several therapies are currently being investigated globally, including nitazoxanide, stem cell therapy, intravenous immunoglobulin, interleukin-6 receptor antagonist (e.g., tocilizumab, sarilumab, and siltuximab), Bacille Calmette-Guerin (BCG) vaccine, angiotensin-II receptor antagonists, and other antivirals (e.g., oseltamivir, danoprevir, darunavir, ganciclovir, favipiravir, baloxavir marboxil, umifenovir, sofosbuvir, ribavirin, and interferon alfa/β).

The most effective long-term strategy for prevention of future outbreaks of this virus would be the development of a vaccine providing protective active immunity. As of April 8, 2020, the global COVID-19 vaccine research and development landscape included 115 vaccine candidates. Out of 78 confirmed active projects, 73 are currently at preclinical stages. 22 A few vaccine candidates have moved into clinical trial phase, including mRNA-1273 (Moderna), Ad5-nCoV (CanSino Biologicals), INO-4800 (Inovio), LV-SMENP-DC, and pathogen-specific aAPC (Shenzhen Geno-Immune Medical Institute). Unfortunately, a vaccine is unlikely to be ready for use before the end of 2020 or 2021 at the earliest.

WHO and Centers for Disease Control and Prevention guidance emphasizes the role of supportive care based on severity of illness, ranging from symptomatic treatment for mild disease to evidence-based ventilator management for ARDS, and early recognition and treatment of bacterial infections and sepsis in critically ill patients. Use of routine systematic corticosteroids should be avoided for the treatment of COVID-19. There is currently no strong evidence of efficacy of HCQ/chloroquine and remdesivir or other antivirals in the treatment or prevention of COVID-19. The FDA and EMA has granted an emergency-use authorization for chloroquine/ HCQ to treat patients when a clinical trial is not available or participation is not feasible. The ICMR recommends the use of HCQ for prophylaxis of SARS-CoV-2 infection in high-risk cases. The EMA recommends use of remdesivir for COVID-19 on a compassionate basis. Guidelines are issued for use of convalescent plasma in patients with serious or immediately life-threatening COVID-19. Data from several ongoing randomized controlled trials will provide further evidence regarding the safety and efficacy of these drugs for COVID-19.

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Compassionate use of remdesivir for patients with severe COVID-19

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None declared.