Heterologous SARS-CoV-2 spike protein booster elicits durable and broad antibody responses against the receptor-binding domain.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
15 03 2023
Historique:
received: 30 08 2022
accepted: 03 03 2023
entrez: 16 3 2023
pubmed: 17 3 2023
medline: 21 3 2023
Statut: epublish

Résumé

The immunogenicity of mRNA vaccines has not been well studied when compared to different vaccine modalities in the context of additional boosters. Here we show that longitudinal analysis reveals more sustained SARS-CoV-2 spike receptor-binding domain (RBD)-binding IgG titers with the breadth to antigenically distinct variants by the S-268019-b spike protein booster compared to the BNT162b2 mRNA homologous booster. The durability and breadth of RBD-angiotensin-converting enzyme 2 (ACE2) binding inhibitory antibodies are pronounced in the group without systemic adverse events (AEs) after the S-268019-b booster, leading to the elevated neutralizing activities against Omicron BA.1 and BA.5 variants in the stratified group. In contrast, BNT162b2 homologous booster elicited antibodies to spike N-terminal domain in proportion to the AE scores. High-dimensional immune profiling identifies early CD16

Identifiants

pubmed: 36922492
doi: 10.1038/s41467-023-37128-1
pii: 10.1038/s41467-023-37128-1
pmc: PMC10016167
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
BNT162 Vaccine 0
Immunoglobulin G 0
S-268019-b COVID-19 vaccine 0
Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0
COVID-19 Vaccines 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1451

Informations de copyright

© 2023. The Author(s).

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Auteurs

Tomohiro Takano (T)

Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.

Takashi Sato (T)

Tokyo Shinagawa Hospital, Tokyo, 140-8522, Japan.

Ryutaro Kotaki (R)

Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.

Saya Moriyama (S)

Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.

Shuetsu Fukushi (S)

Department of Virology I, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.

Masahiro Shinoda (M)

Tokyo Shinagawa Hospital, Tokyo, 140-8522, Japan.

Kiyomi Kabasawa (K)

Tokyo Shinagawa Hospital, Tokyo, 140-8522, Japan.

Nagashige Shimada (N)

Tokyo Shinagawa Hospital, Tokyo, 140-8522, Japan.

Mio Kousaka (M)

Tokyo Shinagawa Hospital, Tokyo, 140-8522, Japan.

Yu Adachi (Y)

Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.

Taishi Onodera (T)

Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.

Kazutaka Terahara (K)

Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.

Masanori Isogawa (M)

Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.

Takayuki Matsumura (T)

Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan. matt@niid.go.jp.

Masaharu Shinkai (M)

Tokyo Shinagawa Hospital, Tokyo, 140-8522, Japan. shinkai050169@gmail.com.

Yoshimasa Takahashi (Y)

Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan. ytakahas@niid.go.jp.

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Classifications MeSH