Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity.

COVID-19 RBD SARS-CoV-2 escape neutralizing antibodies spike variants

Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
12 Mar 2021
Historique:
pubmed: 24 2 2021
medline: 24 2 2021
entrez: 23 2 2021
Statut: epublish

Résumé

Vaccination elicits immune responses capable of potently neutralizing SARS-CoV-2. However, ongoing surveillance has revealed the emergence of variants harboring mutations in spike, the main target of neutralizing antibodies. To understand the impact of these variants, we evaluated the neutralization potency of 99 individuals that received one or two doses of either BNT162b2 or mRNA-1273 vaccines against pseudoviruses representing 10 globally circulating strains of SARS-CoV-2. Five of the 10 pseudoviruses, harboring receptor-binding domain mutations, including K417N/T, E484K, and N501Y, were highly resistant to neutralization. Crossneutralization of B.1.351 variants was comparable to SARS-CoV and bat-derived WIV1-CoV, suggesting that a relatively small number of mutations can mediate potent escape from vaccine responses. While the clinical impact of neutralization resistance remains uncertain, these results highlight the potential for variants to escape from neutralizing humoral immunity and emphasize the need to develop broadly protective interventions against the evolving pandemic.

Identifiants

pubmed: 33619506
doi: 10.1101/2021.02.14.21251704
pmc: PMC7899476
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIAID NIH HHS
ID : T32 AI007245
Pays : United States

Commentaires et corrections

Type : UpdateIn
Type : UpdateIn

Déclaration de conflit d'intérêts

DECLARATIONS OF INTEREST The authors declare no competing interests.

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Auteurs

Wilfredo F Garcia-Beltran (WF)

These authors contributed equally.
Department of Pathology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Department of Pathology, Brigham and Women's Hospital, Boston, MA, 02115, USA.

Evan C Lam (EC)

These authors contributed equally.
Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA, 02139, USA.

Kerri St Denis (K)

These authors contributed equally.
Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA, 02139, USA.

Adam D Nitido (AD)

Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA, 02139, USA.

Zeidy H Garcia (ZH)

Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA, 02139, USA.

Blake M Hauser (BM)

Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA, 02139, USA.

Jared Feldman (J)

Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA, 02139, USA.

Maia N Pavlovic (MN)

Vaccine and Immunotherapy Center, Massachusetts General Hospital, Boston, MA, 02129, USA.

David J Gregory (DJ)

Vaccine and Immunotherapy Center, Massachusetts General Hospital, Boston, MA, 02129, USA.
Pedriatric Infectious Disease, Massachusetts General Hospital for Children, Boston, MA 02114, USA.

Mark C Poznansky (MC)

Vaccine and Immunotherapy Center, Massachusetts General Hospital, Boston, MA, 02129, USA.
Department of Medicine, Massachusetts General Hospital, Boston, MA, 02114, USA.

Alex Sigal (A)

Africa Health Research Institute, Durban, 4001, South Africa.
School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban, 4041 South Africa.
Max Planck Institute for Infection Biology, Berlin, 10117, Germany.

Aaron G Schmidt (AG)

Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA, 02139, USA.

A John Iafrate (AJ)

Department of Pathology, Massachusetts General Hospital, Boston, MA, 02114, USA.

Vivek Naranbhai (V)

Department of Medicine, Massachusetts General Hospital, Boston, MA, 02114, USA.
Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Center for the AIDS Programme of Research in South Africa, Durban, 4001, South Africa.

Alejandro B Balazs (AB)

Ragon Institute of MGH, MIT, and Harvard, Cambridge, MA, 02139, USA.

Classifications MeSH