Plasma and memory antibody responses to Gamma SARS-CoV-2 provide limited cross-protection to other variants
Author(s) -
Marianna Agudelo,
Frauke Muecksch,
Dennis Schaefer-Babajew,
Alice Cho,
Justin DaSilva,
Eva Bednarski,
Víctor Ramos,
Thiago Y. Oliveira,
Melissa Cipolla,
Anna Gazumyan,
Shuai Zong,
Danielle A. S. Rodrigues,
Guilherme S. Lira,
Luciana Conde,
Renato Santana Aguiar,
Orlando C. Ferreira,
Amílcar Tanuri,
Katia C. Affonso,
Rafael Mello Galliez,
Terezinha Marta Pereira Pinto Castiñeiras,
Juliana EchevarriaLima,
Marcelo T. Bozza,
André M. Vale,
Paul D. Bieniasz,
Théodora Hatziioannou,
Michel C. Nussenzweig
Publication year - 2022
Publication title -
the journal of experimental medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 8.483
H-Index - 448
eISSN - 1540-9538
pISSN - 0022-1007
DOI - 10.1084/jem.20220367
Subject(s) - antibody , virology , neutralization , monoclonal antibody , neutralizing antibody , epitope , vaccination , covid-19 , immunology , biology , beta (programming language) , medicine , disease , pathology , computer science , infectious disease (medical specialty) , programming language
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to be a global problem in part because of the emergence of variants of concern that evade neutralization by antibodies elicited by prior infection or vaccination. Here we report on human neutralizing antibody and memory responses to the Gamma variant in a cohort of hospitalized individuals. Plasma from infected individuals potently neutralized viruses pseudotyped with Gamma SARS-CoV-2 spike protein, but neutralizing activity against Wuhan-Hu-1-1, Beta, Delta, or Omicron was significantly lower. Monoclonal antibodies from memory B cells also neutralized Gamma and Beta pseudoviruses more effectively than Wuhan-Hu-1. 69% and 34% of Gamma-neutralizing antibodies failed to neutralize Delta or Wuhan-Hu-1. Although Class 1 and 2 antibodies dominate the response to Wuhan-Hu-1 or Beta, 54% of antibodies elicited by Gamma infection recognized Class 3 epitopes. The results have implications for variant-specific vaccines and infections, suggesting that exposure to variants generally provides more limited protection to other variants.
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