Anti-spike protein antibody titer at the time of breakthrough infection of SARS-CoV-2 omicron.


Journal

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy
ISSN: 1437-7780
Titre abrégé: J Infect Chemother
Pays: Netherlands
ID NLM: 9608375

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 03 02 2022
revised: 02 03 2022
accepted: 23 03 2022
pubmed: 11 4 2022
medline: 14 5 2022
entrez: 10 4 2022
Statut: ppublish

Résumé

By December 2021, about 80% of people over the age of 12 had been vaccinated in Japan, and almost all people were vaccinated with the mRNA vaccine. We investigated here the anti-spike protein antibody titer at the time of breakthrough infection of SARS-CoV-2 omicron. A total of 32 SARS-CoV2 omicron breakthrough infection was included in the study. The median antibody titer at breakthrough infection was 776 AU/mL overall, of which the median antibody titer of BNT162b2 vaccinated was 633 AU/mL and that of mRNA-1273 vaccinated was 9416 AU/mL. This result suggests that low levels of antibody titers 6 months after vaccination do not provide sufficient antibodies to prevent the omicron variant breakthrough infection, which may occur with a higher anti-spike antibody titer after vaccination with mRNA-1273. However, antibody titers in some patients were comparable to those immediately after the second vaccination with either mRNA vaccine.

Identifiants

pubmed: 35397976
pii: S1341-321X(22)00100-3
doi: 10.1016/j.jiac.2022.03.021
pmc: PMC8971116
pii:
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0
RNA, Viral 0
Vaccines, Synthetic 0
mRNA Vaccines 0
BNT162 Vaccine N38TVC63NU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1015-1017

Informations de copyright

Copyright © 2022 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

Références

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pubmed: 34995482
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pubmed: 34320281
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pubmed: 34901897
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pubmed: 34165323
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pubmed: 34385356
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pubmed: 35063123
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pubmed: 35062724
Nat Med. 2021 Jul;27(7):1205-1211
pubmed: 34002089
Emerg Microbes Infect. 2022 Dec;11(1):1-5
pubmed: 34890524

Auteurs

Eisuke Adachi (E)

Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of the Institute of Medical Science, The University of Tokyo, Tokyo, Japan. Electronic address: eadachi-ims@umin.ac.jp.

Etsuko Nagai (E)

Department of Laboratory Medicine, IMSUT Hospital of the Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

Makoto Saito (M)

Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Tokyo, Japan.

Masamichi Isobe (M)

Department of Hematology/Oncology IMSUT Hospital of the Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

Takaaki Konuma (T)

Division of Hematopoietic Disease Control, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Tokyo, Japan.

Michiko Koga (M)

Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Tokyo, Japan.

Takeya Tsutsumi (T)

Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Tokyo, Japan.

Yasuhito Nannya (Y)

Department of Hematology/Oncology IMSUT Hospital of the Institute of Medical Science, The University of Tokyo, Tokyo, Japan; Division of Hematopoietic Disease Control, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Tokyo, Japan.

Hiroshi Yotsuyanagi (H)

Department of Infectious Diseases and Applied Immunology, IMSUT Hospital of the Institute of Medical Science, The University of Tokyo, Tokyo, Japan; Division of Infectious Diseases, Advanced Clinical Research Center, Institute of Medical Science, University of Tokyo, Tokyo, Japan.

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Classifications MeSH