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Nucleocapsid-specific antibody function is associated with therapeutic benefit from Covid-19 Convalescent plasma therapy

Authors :
Massachusetts Institute of Technology. Department of Biological Engineering
Herman, Jonathan D
Wang, Chuangqi
Burke, John Stephen
Zur, Yonatan
Compere, Hacheming
Kang, Jaewon
Macvicar, Ryan
Taylor, Sabian
Shin, Sally
Frank, Ian
Siegel, Don
Tebas, Pablo
Choi, Grace H
Shaw, Pamela A
Yoon, Hyunah
Pirofski, Liise-anne
Julg, Boris D
Bar, Katharine J
Lauffenburger, Douglas
Alter, Galit
Massachusetts Institute of Technology. Department of Biological Engineering
Herman, Jonathan D
Wang, Chuangqi
Burke, John Stephen
Zur, Yonatan
Compere, Hacheming
Kang, Jaewon
Macvicar, Ryan
Taylor, Sabian
Shin, Sally
Frank, Ian
Siegel, Don
Tebas, Pablo
Choi, Grace H
Shaw, Pamela A
Yoon, Hyunah
Pirofski, Liise-anne
Julg, Boris D
Bar, Katharine J
Lauffenburger, Douglas
Alter, Galit
Source :
Elsevier
Publication Year :
2023

Abstract

Coronavirus disease 2019 (COVID-19) convalescent plasma (CCP), a passive polyclonal antibody therapeutic agent, has had mixed clinical results. Although antibody neutralization is the predominant approach to benchmarking CCP efficacy, CCP may also influence the evolution of the endogenous antibody response. Using systems serology to comprehensively profile severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) functional antibodies of hospitalized people with COVID-19 enrolled in a randomized controlled trial of CCP (ClinicalTrials.gov: NCT04397757), we find that the clinical benefits of CCP are associated with a shift toward reduced inflammatory Spike (S) responses and enhanced nucleocapsid (N) humoral responses. We find that CCP has the greatest clinical benefit in participants with low pre-existing anti-SARS-CoV-2 antibody function and that CCP-induced immunomodulatory Fc glycan profiles and N immunodominant profiles persist for at least 2 months. We highlight a potential mechanism of action of CCP associated with durable immunomodulation, outline optimal patient characteristics for CCP treatment, and provide guidance for development of a different class of COVID-19 hyperinflammation-targeting antibody therapeutic agents.

Details

Database :
OAIster
Journal :
Elsevier
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1370256082
Document Type :
Electronic Resource