2020
DOI: 10.1016/j.imbio.2020.152001
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Endothelial injury and thrombotic microangiopathy in COVID-19: Treatment with the lectin-pathway inhibitor narsoplimab

Abstract: Highlights Narsoplimab down-modulates SARS-CoV-2-induced activation of the lectin pathway and endothelial cell damage. Narsoplimab can reduce the thrombotic risk of Covid-19 patients. All patients treated with narsoplimab improved and survived without any drug-related adverse events.

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Cited by 131 publications
(150 citation statements)
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“…BK virus and human herpesvirus 6, might be potential causative factors of TA-TMA [29,30]. A relative ADAMTS13 deficiency [31], increased circulating endothelial cell (CEC) counts and serum levels of IL-6 and IL-8 [32] are observed in COVID-19, reminiscent the findings in TMA. Urokinase plasminogen activator receptor (uPAR) is bound on the endothelium and released into the blood stream as a soluble counterpart, named suPAR, in the setting of inflammation and endothelial damage [33].…”
Section: Endothelial Dysfunction and Thrombotic Microangiopathymentioning
confidence: 93%
See 1 more Smart Citation
“…BK virus and human herpesvirus 6, might be potential causative factors of TA-TMA [29,30]. A relative ADAMTS13 deficiency [31], increased circulating endothelial cell (CEC) counts and serum levels of IL-6 and IL-8 [32] are observed in COVID-19, reminiscent the findings in TMA. Urokinase plasminogen activator receptor (uPAR) is bound on the endothelium and released into the blood stream as a soluble counterpart, named suPAR, in the setting of inflammation and endothelial damage [33].…”
Section: Endothelial Dysfunction and Thrombotic Microangiopathymentioning
confidence: 93%
“…Patients with severe COVID-19 treated with narsoplimab (anti-MASP-2 antibody) under compassionate use displayed rapid and sustained reduction in markers of endothelial damage (CECs, IL-6, IL-8, CRP and LDH levels). All patients treated with narsoplimab recovered and the agents is being evaluated further in patients with severe COVID-19 [32]. As mentioned above, the laboratory and autopsy findings in COVID-19 reminiscent of one seen in TMA, which is also highly associated with pathogenic complement activation [25].…”
Section: Complement Activation In Covid-19mentioning
confidence: 99%
“…In addition, a clinical trial (ChiCTR2000029765) of tocilizumab for the treatment of COVID-19 is currently underway. Other monoclonal antibodies specific for proinflammatory cytokines also show prospects for treating COVID-19, which include Canakinumab, a monoclonal antibody targeting IL-1b (56); Eculizumab, C5-targeting monoclonal antibody (57); Narsoplimab, a monoclonal antibody against mannose-binding protein-associated serine protease 2 (58); and Dupilumab, a monoclonal antibody of the immunoglobulin G4 subclass (59).…”
Section: Monoclonal Antibodies Specific For Inflammatory Cytokinesmentioning
confidence: 99%
“…In contrast, Holter et al (125) did not find much difference in MBL concentrations in plasma between COVID-19 patients and controls although a transient increase of its level (at days 3-5 after hospital admission) was noted. It should be however stressed that narsoplimab, specifically targeting MASP-2, has recently been demonstrated to be a promising therapeutic agent, reducing detrimental effects of complement activation and giving no adverse reactions itself (126).…”
Section: Possible Associations Of Complement Activation Via the Lectimentioning
confidence: 99%