Progressive loss of conserved spike protein neutralizing antibody sites in Omicron sublineages is balanced by preserved T cell immunity.
CP: Immunology
SARS-CoV-2
T cell immunity
epitope conservedness
immune escape
neutralizing antibodies
Journal
Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691
Informations de publication
Date de publication:
29 08 2023
29 08 2023
Historique:
received:
17
03
2023
revised:
27
03
2023
accepted:
13
07
2023
medline:
4
9
2023
pubmed:
1
8
2023
entrez:
1
8
2023
Statut:
ppublish
Résumé
Evolution of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant has led to the emergence of sublineages with different patterns of neutralizing antibody evasion. We report that Omicron BA.4/BA.5 breakthrough infection of individuals immunized with SARS-CoV-2 wild-type-strain-based mRNA vaccines results in a boost of Omicron BA.4.6, BF.7, BQ.1.1, and BA.2.75 neutralization but does not efficiently boost BA.2.75.2, XBB, or XBB.1.5 neutralization. In silico analyses showed that the Omicron spike glycoprotein lost most neutralizing B cell epitopes, especially in sublineages BA.2.75.2, XBB, and XBB.1.5. In contrast, T cell epitopes are conserved across variants including XBB.1.5. T cell responses of mRNA-vaccinated, SARS-CoV-2-naive individuals against the wild-type strain, Omicron BA.1, and BA.4/BA.5 were comparable, suggesting that T cell immunity against recent sublineages including XBB.1.5 may remain largely unaffected. While some Omicron sublineages effectively evade B cell immunity, spike-protein-specific T cell immunity, due to the nature of polymorphic cell-mediated immune responses, may continue to contribute to prevention/limitation of severe COVID-19 manifestation.
Identifiants
pubmed: 37527039
pii: S2211-1247(23)00899-9
doi: 10.1016/j.celrep.2023.112888
pii:
doi:
Substances chimiques
spike protein, SARS-CoV-2
0
Spike Glycoprotein, Coronavirus
0
Antibodies, Neutralizing
0
Antibodies, Viral
0
Banques de données
ClinicalTrials.gov
['NCT05004181', 'NCT04955626']
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
112888Informations de copyright
Copyright © 2023 BioNTech SE. Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests U.S. and O.T. are management board members and employees at BioNTech SE. A.M., B.G.L., J.Q., M.B., A.T., J. Gordon, J. Grosser, I.V., and O.O. are employees at BioNTech SE. A.P. and H.D. are employees at BioNTech US. Y.F. and K.B. are employees of InstaDeep, Ltd. K.G., N.K., S.H., and S.C. are employees at the University Hospital, Goethe University Frankfurt. U.S., O.T., A.P., and A.M. are inventors on patents and patent applications related to RNA technology and COVID-19 vaccines. U.S., O.T., A.M., B.G.L., J.Q., M.B., A.T. A.P., H.D., J. Gordon, J. Grosser, I.V., and O.O. have securities from BioNTech SE. S.C. has received an honorarium for serving on a clinical advisory board for BioNTech SE.