Evaluation of Cellular and Serological Responses to Acute SARS-CoV-2 Infection Demonstrates the Functional Importance of the Receptor-Binding Domain.


Journal

Journal of immunology (Baltimore, Md. : 1950)
ISSN: 1550-6606
Titre abrégé: J Immunol
Pays: United States
ID NLM: 2985117R

Informations de publication

Date de publication:
01 06 2021
Historique:
received: 18 12 2020
accepted: 18 03 2021
pubmed: 7 5 2021
medline: 8 6 2021
entrez: 6 5 2021
Statut: ppublish

Résumé

The factors that control the development of an effective immune response to the recently emerged SARS-CoV-2 virus are poorly understood. In this study, we provide a cross-sectional analysis of the dynamics of B cell responses to SARS-CoV-2 infection in hospitalized COVID-19 patients. We observe changes in B cell subsets consistent with a robust humoral immune response, including significant expansion of plasmablasts and activated receptor-binding domain (RBD)-specific memory B cell populations. We observe elevated titers of Abs to SARS-CoV-2 RBD, full-length Spike, and nucleoprotein over the course of infection, with higher levels of RBD-specific IgG correlating with increased serum neutralization. Depletion of RBD-specific Abs from serum removed a major portion of neutralizing activity in most individuals. Some donors did retain significant residual neutralization activity, suggesting a potential Ab subset targeting non-RBD epitopes. Taken together, these findings are instructive for future vaccine design and mAb strategies.

Identifiants

pubmed: 33952616
pii: jimmunol.2001420
doi: 10.4049/jimmunol.2001420
pmc: PMC8482837
mid: NIHMS1685839
doi:

Substances chimiques

Nucleocapsid Proteins 0
Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0

Types de publication

Evaluation Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2605-2613

Subventions

Organisme : NIAID NIH HHS
ID : U01 AI150747
Pays : United States
Organisme : NIH HHS
ID : P51 OD011132
Pays : United States
Organisme : NIA NIH HHS
ID : R00 AG049092
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI057266
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI148684
Pays : United States
Organisme : NIAID NIH HHS
ID : R24 AI120942
Pays : United States

Informations de copyright

Copyright © 2021 by The American Association of Immunologists, Inc.

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Auteurs

Grace Mantus (G)

Centers for Childhood Infections and Vaccines, Children's Healthcare of Atlanta and Emory University, Department of Pediatrics, Atlanta, GA.
Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.

Lindsay E Nyhoff (LE)

Centers for Childhood Infections and Vaccines, Children's Healthcare of Atlanta and Emory University, Department of Pediatrics, Atlanta, GA.
Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.

Robert C Kauffman (RC)

Centers for Childhood Infections and Vaccines, Children's Healthcare of Atlanta and Emory University, Department of Pediatrics, Atlanta, GA.
Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.

Venkata Viswanadh Edara (VV)

Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
Division of Infectious Diseases, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
Yerkes National Primate Research Center, Atlanta, GA.

Lilin Lai (L)

Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
Division of Infectious Diseases, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
Yerkes National Primate Research Center, Atlanta, GA.

Katharine Floyd (K)

Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
Division of Infectious Diseases, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.
Yerkes National Primate Research Center, Atlanta, GA.

Pei-Yong Shi (PY)

Department of Microbiology and Immunology, Institute for Human Infection and Immunity, World Reference Center for Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, TX.

Vineet D Menachery (VD)

Department of Biochemistry and Molecular Biology, The University of Texas Medical Branch, Galveston, TX.

Srilatha Edupuganti (S)

Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine Decatur, Atlanta, GA; and.

Erin M Scherer (EM)

Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine Decatur, Atlanta, GA; and.

Ariel Kay (A)

Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine Decatur, Atlanta, GA; and.

Nina McNair (N)

Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine Decatur, Atlanta, GA; and.

Evan J Anderson (EJ)

Centers for Childhood Infections and Vaccines, Children's Healthcare of Atlanta and Emory University, Department of Pediatrics, Atlanta, GA.

Nadine Rouphael (N)

Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine Decatur, Atlanta, GA; and.

Rafi Ahmed (R)

Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.

Mehul S Suthar (MS)

Centers for Childhood Infections and Vaccines, Children's Healthcare of Atlanta and Emory University, Department of Pediatrics, Atlanta, GA.
Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.
Division of Infectious Diseases, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA.

Jens Wrammert (J)

Centers for Childhood Infections and Vaccines, Children's Healthcare of Atlanta and Emory University, Department of Pediatrics, Atlanta, GA; jwramme@emory.edu.
Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA.

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