key: cord-0970170-lh6e2wga
authors: Eriksson, Oskar; Hultström, Michael; Persson, Barbro; Lipcsey, Miklos; Ekdahl, Kristina Nilsson; Nilsson, Bo; Frithiof, Robert
title: Mannose-Binding Lectin is Associated with Thrombosis and Coagulopathy in Critically Ill COVID-19 Patients
date: 2020-09-01
journal: Thromb Haemost
DOI: 10.1055/s-0040-1715835
sha: b335119d09101f5879d6b1977105d2d3334fd6e4
doc_id: 970170
cord_uid: lh6e2wga

The ongoing COVID-19 pandemic has caused significant morbidity and mortality worldwide, as well as profound effects on society. COVID-19 patients have an increased risk of thromboembolic (TE) complications, which develop despite pharmacological thromboprophylaxis. The mechanism behind COVID-19-associated coagulopathy remains unclear. Mannose-binding lectin (MBL), a pattern recognition molecule that initiates the lectin pathway of complement activation, has been suggested as a potential amplifier of blood coagulation during thromboinflammation. Here we describe data from a cohort of critically ill COVID-19 patients ( n = 65) treated at a tertiary hospital center intensive care unit (ICU). A subset of patients had strongly elevated MBL plasma levels, and activity upon ICU admission, and patients who developed symptomatic TE (14%) had significantly higher MBL levels than patients without TE. MBL was strongly correlated to plasma D-dimer levels, a marker of COVID-19 coagulopathy, but showed no relationship to degree of inflammation or other organ dysfunction. In conclusion, we have identified complement activation through the MBL pathway as a novel amplification mechanism that contributes to pathological thrombosis in critically ill COVID-19 patients. Pharmacological targeting of the MBL pathway could be a novel treatment option for thrombosis in COVID-19. Laboratory testing of MBL levels could be of value for identifying COVID-19 patients at risk for TE events.

a plasma-based branch of the innate immune system, has been suggested to be involved in COVID-19 pathogenesis by exacerbating systemic inflammation and tissue damage and by amplifying the prothrombotic state. 4 Specifically, mannosebinding lectin (MBL), a pattern recognition molecule that initiates the lectin pathway of complement activation, binds to coronaviruses 5 and has been proposed to participate in the host defense during COVID-19 infection. 6 To clarify the role of MBL in COVID-19 we measured plasma MBL levels and activity in a cohort of critically ill COVID-19 patients and investigated its relation to clinical outcome. A prospective single-center observational study was performed at the intensive care unit (ICU) of a tertiary hospital in Uppsala, Sweden (ClinicalTrials ID: NCT04316884). The study was approved by the Swedish National Ethical Review Agency (EPM; No. 2020-01623). Informed consent was obtained in patients with no thrombosis, p ¼ 0.028). Results are expressed as medians and interquartile ranges (IQRs). p-Values were calculated using the Mann-Whitney U test. from the patient, or next of kin if the patient was unable give consent. The Declaration of Helsinki and its subsequent revisions were followed. All patients > 18 years of age with confirmed or suspected COVID-19 admitted to the ICU between March 13 and April 30, 2020, were screened for inclusion. Informed consents were given by 70 out of 71 screened patients. Two patients were excluded due to negative polymerase chain reaction for severe acute respiratory syndrome coronavirus 2. For two patients no initial blood sample was available. One patient was transferred from the ICU at another hospital and thus excluded. The remaining 65 patients were enrolled in the study.

Blood was sampled in ethylenediaminetetraacetic acid tubes, and plasma stored at -70°C until analysis. Plasma MBL levels at day 1 at the ICU (on average COVID-19 day 10) were measured by an in-house enzyme-linked immunosorbent assay (ELISA), and were significantly higher than in healthy controls (►Fig. 1A). Activity of the MBL pathway was assessed by a functional ELISA using mannan as activator and MBL binding capacity and complement C3 deposition as readouts. 7 This assay measures the functional MBL concentration in plasma and its capacity to activate complement, and confirmed elevated MBL activity and MBL-dependent C3 deposition in the patient group (►Fig. 1B).

Plasma Patients with TE had significantly higher MBL levels compared with patients without TE, and MBL activity and MBLdependent C3 deposition showed the same relationship. Of the nine TEs, two were arterial thrombosis (stroke or myocardial infarction) and seven were pulmonary embolisms (PEs), in agreement with observations that PE is a frequent complication in COVID-19 patients. 8, 9 Interestingly, patients who developed PE all had MBL levels above the 95th percentile in controls (►Fig. 1C, D).

We next investigated the relationship between MBL levels and laboratory markers of coagulation activity, measured on the day of ICU admission (►Table 1). MBL displayed a strong correlation with plasma D-dimer levels, corroborating the clinical association with TE. MBL was also significantly correlated to activated partial thromboplastin time, but not with prothrombin time or prothrombin fragment 1 þ 2. Interestingly, MBL appeared to specifically associate with biochemical markers of coagulation. No relationship Abbreviations: aB-pO 2 /FiO 2 , arterial blood gas oxygen tension ratio to percentage of inspired oxygen; APPT, activated partial thromboplastin test; CRP, Creactive protein; ELISA, enzyme-linked immunosorbent assay; F 1 þ 2, fragment 1 þ 2; INR, international normalized ratio; IQR, interquartile range; MBL, mannose-binding lectin; NHS, normal human serum; NT-proBNP, N-terminal fragment of probrain natriuretic peptide; P-, plasma; PT prothrombin time. Note: Correlations were assessed by calculating Spearman's rank correlation coefficient (Spearman's r). Clinical chemistry test results were collected from the patients' clinical records, except C3, C3d, and C1q, which were measured by in-house methods, and prothrombin F 1 þ 2, which was measured by a commercial ELISA (Enzygnost F 1 þ 2, Siemens Healthcare).

Boldfaced values indicate statistically significant correlations (p-Value < 0.05).

COVID-19 and coagulation: bleeding and thrombotic manifestations of SARS-CoV-2 infection

COVID-19-related severe hypercoagulability in patients admitted to intensive care unit for acute respiratory failure

Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study

Complement activation in patients with COVID-19: a novel therapeutic target

Mannose-binding lectin in severe acute respiratory syndrome coronavirus infection

Highly pathogenic coronavirus N protein aggravates lung injury by MASP-2-mediated complement over-activation

Sodium polyanethole sulfonate as an inhibitor of activation of complement function in blood culture systems

Confirmation of the high cumulative incidence of thrombotic complications in critically ill ICU patients with COVID-19: an updated analysis

Pulmonary embolism or pulmonary thrombosis in COVID-19? Is the recommendation to use high-dose heparin for thromboprophylaxis justified?

Mannose binding lectin acute phase activity in patients with severe infection

Acute-phase responsiveness of mannose-binding lectin in community-acquired pneumonia is highly dependent upon MBL2 genotypes

Mannosebinding lectin does not act as an acute-phase reactant in adults with community-acquired pneumococcal pneumonia

Interpretation of serological complement biomarkers in disease

The human platelet as an innate immune cell: interactions between activated platelets and the complement system

A journey through the lectin pathway of complement-MBL and beyond

The lectin complement pathway serine proteases (MASPs) represent a possible crossroad between the coagulation and complement systems in thromboinflammation

Effects of MASP-1 of the complement system on activation of coagulation factors and plasma clot formation

Human mannose-binding lectin inhibitor prevents myocardial injury and arterial thrombogenesis in a novel animal model

Targeting mannose-binding lectin confers long-lasting protection with a surprisingly wide therapeutic window in cerebral ischemia

Plasma levels of mannosebinding lectin and future risk of venous thromboembolism

Clinical promise of nextgeneration complement therapeutics

The technical expertise of Sliva Abdalla is greatly appreciated. The authors thank the study nurses Elin Söderberg and Joanna Wessbergh, and the biobank research assistants Philip Karlsson and Erik Danielsson.

was found between MBL and markers of cardiac (N-terminal fragment of probrain natriuretic peptide) or respiratory function (pO 2 /FiO 2 ratio), nor with markers of inflammation (C-reactive protein, interleukin-6, or ferritin), in line with observations that MBL is not a typical acute phase reactant. [10] [11] [12] MBL showed a significant correlation with total complement factor C3 levels, but not with the activation product C3d (measured as C3d/C3 ratio), a measure of activity of the alternative pathway of complement, nor with C1q, the initiator of the classical pathway. 13 Total C3 levels, C3d/C3 ratio, or C1q were not related to thrombotic events (p ¼ 0.75, 0.57, and 0.28, respectively), indicating a specific association between MBL and thrombosis.Our observations do not prove a causal role for MBL in thrombosis. Nonetheless, preclinical data implicate MBL as a key prothrombotic factor. MBL circulates in complex with the serine proteases mannose-associated serine protease (MASP)-1 and MASP-2, which activate the complement cascade upon MBL target binding. 14 The MASPs intriguingly display coagulation factor-like substrate specificities 15 and are activated during blood clotting. 16 MASP-1 promotes clot formation by multiple mechanisms, including direct activation of factor XIII (FXIII) that cross-links fibrin. 17 In addition, pharmacological or genetic targeting of the MBL pathway in mice provides protection from thrombosis, 18, 19 and MBL has been associated with thrombosis in epidemiological studies. 20 The standard choice for thromboprophylaxis in COVID-19 patients is low-molecular-weight heparin (LMWH), which preferentially targets FXa. Here, MBL-associated MASPs could act as a LMWH bypass mechanism to directly promote fibrin formation, and indeed, all the TE events in our study occurred despite thromboprophylaxis. As therapeutics targeting the MBL pathway are currently in clinical trials, 21 this could be an alternative strategy for antithrombotic treatment in COVID-19.A limitation of our study is that we did not assess the relationship between MBL and thrombosis in critically ill patients without COVID-19. Nonetheless, our data indicate a role for the MBL branch of the complement system in COVID-19-associated coagulopathy and we propose that measurement of plasma MBL could be of value to identify COVID-19 patients at high risk of thrombosis.

All authors participated in conception and design of the study. O.E. performed MBL activity assay, analyzed data, and prepared the manuscript. Thereafter, all authors had access to the data and participated in data collection and interpretation. All authors contributed to manuscript revision and gave approval of the final version. 

None declared.