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Antibodies from convalescent plasma promote SARS-CoV-2 clearance in individuals with and without endogenous antibody response
Maddalena Marconato, … , Markus G. Manz, Alexandra Trkola
Maddalena Marconato, … , Markus G. Manz, Alexandra Trkola
Published April 28, 2022
Citation Information: J Clin Invest. 2022;132(12):e158190. https://doi.org/10.1172/JCI158190.
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Clinical Research and Public Health

Antibodies from convalescent plasma promote SARS-CoV-2 clearance in individuals with and without endogenous antibody response

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Abstract

BACKGROUND Neutralizing antibodies are considered a key correlate of protection by current SARS-CoV-2 vaccines. The manner in which human infections respond to therapeutic SARS-CoV-2 antibodies, including convalescent plasma therapy, remains to be fully elucidated.METHODS We conducted a proof-of-principle study of convalescent plasma therapy based on a phase I trial in 30 hospitalized COVID-19 patients with a median interval between onset of symptoms and first transfusion of 9 days (IQR, 7–11.8 days). Comprehensive longitudinal monitoring of the virological, serological, and disease status of recipients allowed deciphering of parameters on which plasma therapy efficacy depends.RESULTS In this trial, convalescent plasma therapy was safe as evidenced by the absence of transfusion-related adverse events and low mortality (3.3%). Treatment with highly neutralizing plasma was significantly associated with faster virus clearance, as demonstrated by Kaplan-Meier analysis (P = 0.034) and confirmed in a parametric survival model including viral load and comorbidity (adjusted hazard ratio, 3.0; 95% CI, 1.1–8.1; P = 0.026). The onset of endogenous neutralization affected viral clearance, but even after adjustment for their pretransfusion endogenous neutralization status, recipients benefitted from plasma therapy with high neutralizing antibodies (hazard ratio, 3.5; 95% CI, 1.1–11; P = 0.034).CONCLUSION Our data demonstrate a clear impact of exogenous antibody therapy on the rapid clearance of viremia before and after onset of the endogenous neutralizing response, and point beyond antibody-based interventions to critical laboratory parameters for improved evaluation of current and future SARS-CoV-2 therapies.TRIAL REGISTRATION ClinicalTrials.gov NCT04869072.FUNDING This study was funded via an Innovation Pool project by the University Hospital Zurich; the Swiss Red Cross Glückskette Corona Funding; Pandemiefonds of the UZH Foundation; and the Clinical Research Priority Program “Comprehensive Genomic Pathogen Detection” of the University of Zurich.

Authors

Maddalena Marconato, Irene A. Abela, Anthony Hauser, Magdalena Schwarzmüller, Rheliana Katzensteiner, Dominique L. Braun, Selina Epp, Annette Audigé, Jacqueline Weber, Peter Rusert, Eméry Schindler, Chloé Pasin, Emily West, Jürg Böni, Verena Kufner, Michael Huber, Maryam Zaheri, Stefan Schmutz, Beat M. Frey, Roger D. Kouyos, Huldrych F. Günthard, Markus G. Manz, Alexandra Trkola

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Figure 4

Spike-specific binding and neutralizing antibodies in convalescent donor plasma are linked with rapid viral clearance.

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Spike-specific binding and neutralizing antibodies in convalescent donor...
(A) Impact of convalescent donor plasma antibody parameters on the time to viral clearance in recipients (n = 30) was assessed by multivariable parametric survival models. Hazard ratios for individual antibody reactivities adjusted for the presence of comorbidity and the baseline viral load (NPS) are shown. Significant results are marked in red. Low and high binding activity for each individual binding antibody parameter measured in the Elecsys S test (total RBD) and for the ABCORA test parameters is stratified by the respective median binding reactivity. Low and high neutralization activity of transfused convalescent donor plasma is stratified by an NT50 of 250. (B) Forest plot depicting hazard ratios of univariable (black) and multivariable (red) models of time to viral clearance including total S1 (sum of ABCORA IgG, IgA, and IgM reactivity with S1) stratified by the median binding reactivity. Multivariable analyses are corrected for baseline viral load (NPS) and the presence of comorbidity.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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