Effects of potent neutralizing antibodies from convalescent plasma in patients hospitalized for severe SARS-CoV-2 infection
-
Published:2021-05-27
Issue:1
Volume:12
Page:
-
ISSN:2041-1723
-
Container-title:Nature Communications
-
language:en
-
Short-container-title:Nat Commun
Author:
Gharbharan Arvind, Jordans Carlijn C. E., GeurtsvanKessel CorineORCID, den Hollander Jan G., Karim Faiz, Mollema Femke P. N., Stalenhoef – Schukken Janneke E.ORCID, Dofferhoff Anthonius, Ludwig Inge, Koster Adrianus, Hassing Robert-Jan, Bos Jeannet C., van Pottelberge Geert R., Vlasveld Imro N., Ammerlaan Heidi S. M., van Leeuwen – Segarceanu Elena M., Miedema Jelle, van der Eerden Menno, Schrama Thijs J.ORCID, Papageorgiou Grigorios, te Boekhorst Peter, Swaneveld Francis H., Mueller Yvonne M.ORCID, Schreurs Marco W. J., van Kampen Jeroen J. A., Rockx BarryORCID, Okba Nisreen M. A.ORCID, Katsikis Peter D.ORCID, Koopmans Marion P. G.ORCID, Haagmans Bart L.ORCID, Rokx CasperORCID, Rijnders Bart J. A.
Abstract
AbstractIn a randomized clinical trial of 86 hospitalized COVID-19 patients comparing standard care to treatment with 300mL convalescent plasma containing high titers of neutralizing SARS-CoV-2 antibodies, no overall clinical benefit was observed. Using a comprehensive translational approach, we unravel the virological and immunological responses following treatment to disentangle which COVID-19 patients may benefit and should be the focus of future studies. Convalescent plasma is safe, does not improve survival, has no effect on the disease course, nor does plasma enhance viral clearance in the respiratory tract, influence SARS-CoV-2 antibody development or serum proinflammatory cytokines levels. Here, we show that the vast majority of patients already had potent neutralizing SARS-CoV-2 antibodies at hospital admission and with comparable titers to carefully selected plasma donors. This resulted in the decision to terminate the trial prematurely. Treatment with convalescent plasma should be studied early in the disease course or at least preceding autologous humoral response development.
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry
Reference56 articles.
1. RECOVERY Collaborative Group. Dexamethasone in hospitalized patients with Covid-19. N Engl J Med. 384, 693–704 (2021). 2. Beigel, J. H. et al. Remdesivir for the treatment of Covid-19 — final report. N. Engl. J. Med. https://doi.org/10.1056/NEJMoa2007764 (2020). 3. Pan, H. et al. Repurposed antiviral drugs for COVID-19 — interim WHO SOLIDARITY trial results. WHO Solidarity Trial Consortium. N Engl J Med. 384, 497–511 (2021). 4. Study assessing the safety, tolerability, pharmacokinetics, and immunogenicity of repeated subcutaneous doses of anti-spike (S) SARS-CoV-2 monoclonal antibodies (REGN10933+REGN10987) in adult volunteers as related to COVID-19, https://clinicaltrials.gov/ct2/show/study/NCT04519437?term=Regeneron+Pharmaceuticals&cond=%22Coronavirus+Infections%22&draw=2&rank=2#wrapper (accessed 20 October 2020). 5. Safety, tolerability, and efficacy of anti-spike (S) SARS-CoV-2 monoclonal antibodies for the treatment of ambulatory adult patients with COVID-19, https://clinicaltrials.gov/ct2/show/NCT04425629?term=Regeneron+Pharmaceuticals&cond=%22Coronavirus+Infections%22&draw=2&rank=3 (accessed 20 October 2020).
Cited by
138 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|