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Tytuł pozycji:

Effectiveness of the third dose of BNT162b2 vaccine on neutralizing Omicron variant in the Japanese population.

Tytuł:
Effectiveness of the third dose of BNT162b2 vaccine on neutralizing Omicron variant in the Japanese population.
Autorzy:
Kawasuji H; Department of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Morinaga Y; Department of Microbiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan; Clinical and Research Center for Infectious Diseases, Toyama University Hospital, Toyama, Japan. Electronic address: .
Tani H; Department of Microbiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan; Department of Virology, Toyama Institute of Health, Toyama, Japan.
Saga Y; Department of Microbiology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan; Department of Virology, Toyama Institute of Health, Toyama, Japan.
Kaneda M; Department of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Murai Y; Department of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Ueno A; Department of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Miyajima Y; Department of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Fukui Y; Department of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Nagaoka K; Department of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan; Clinical and Research Center for Infectious Diseases, Toyama University Hospital, Toyama, Japan.
Ono C; Laboratory of Virus Control, Center for Infectious Disease Education and Research (CiDER), Osaka University, Osaka, Japan; Laboratory of Virus Control, Research Institute for Microbial Diseases (RIMD), Osaka University, Osaka, Japan.
Matsuura Y; Laboratory of Virus Control, Center for Infectious Disease Education and Research (CiDER), Osaka University, Osaka, Japan; Laboratory of Virus Control, Research Institute for Microbial Diseases (RIMD), Osaka University, Osaka, Japan.
Niimi H; Clinical and Research Center for Infectious Diseases, Toyama University Hospital, Toyama, Japan; Department of Clinical Laboratory and Molecular Pathology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Yamamoto Y; Department of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan; Clinical and Research Center for Infectious Diseases, Toyama University Hospital, Toyama, Japan.
Źródło:
Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy [J Infect Chemother] 2022 Sep; Vol. 28 (9), pp. 1273-1278. Date of Electronic Publication: 2022 Jun 10.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Publication: 2014- : Amsterdam : Elsevier
Original Publication: Tokyo : New York : Published for the Society by Churchill Livingstone, c1995-
MeSH Terms:
Antibodies, Neutralizing*
Antibodies, Viral*
BNT162 Vaccine*/immunology
COVID-19*/prevention & control
Adult ; Aged ; Humans ; Japan ; Middle Aged ; SARS-CoV-2 ; Vaccines, Inactivated ; Young Adult
References:
Lancet. 2021 Dec 18;398(10318):2258-2276. (PMID: 34863358)
Cell. 2022 Feb 3;185(3):447-456.e11. (PMID: 35026151)
Cell. 2021 Jan 21;184(2):476-488.e11. (PMID: 33412089)
Nat Med. 2021 Jul;27(7):1178-1186. (PMID: 33953384)
N Engl J Med. 2021 Sep 23;385(13):1244-1246. (PMID: 34379917)
Microbiol Spectr. 2021 Dec 22;9(3):e0056121. (PMID: 34851162)
N Engl J Med. 2022 Mar 3;386(9):894-896. (PMID: 35081296)
Med (N Y). 2022 Apr 8;3(4):249-261.e4. (PMID: 35261995)
Virol J. 2021 Jan 12;18(1):16. (PMID: 33435994)
Science. 2022 Feb 11;375(6581):678-680. (PMID: 35040667)
N Engl J Med. 2021 Dec 9;385(24):e83. (PMID: 34614327)
Sci Rep. 2021 Aug 16;11(1):16535. (PMID: 34400739)
Nat Commun. 2022 Feb 14;13(1):864. (PMID: 35165284)
Lancet. 2021 Dec 4;398(10316):2093-2100. (PMID: 34756184)
N Engl J Med. 2022 Mar 17;386(11):1088-1091. (PMID: 35081298)
Clin Microbiol Infect. 2022 May;28(5):735.e1-735.e3. (PMID: 35143997)
Lancet. 2022 Jan 15;399(10321):234-236. (PMID: 34942101)
Microbiol Spectr. 2021 Dec 22;9(3):e0056021. (PMID: 34851163)
N Engl J Med. 2021 Oct 7;385(15):1393-1400. (PMID: 34525275)
Lancet Reg Health Eur. 2021 Nov;10:100208. (PMID: 34514454)
Cell. 2022 Feb 3;185(3):457-466.e4. (PMID: 34995482)
MMWR Morb Mortal Wkly Rep. 2021 Oct 01;70(39):1379-1384. (PMID: 34591835)
Clin Microbiol Infect. 2022 Feb;28(2):202-221. (PMID: 34715347)
Contributed Indexing:
Keywords: Anti-receptor binding domain antibody; BNT162b2; Booster; Neutralizing antibody; Omicron
Substance Nomenclature:
0 (Antibodies, Neutralizing)
0 (Antibodies, Viral)
0 (Vaccines, Inactivated)
N38TVC63NU (BNT162 Vaccine)
SCR Organism:
SARS-CoV-2 variants
Entry Date(s):
Date Created: 20220612 Date Completed: 20220706 Latest Revision: 20221024
Update Code:
20240105
PubMed Central ID:
PMC9186405
DOI:
10.1016/j.jiac.2022.05.009
PMID:
35691864
Czasopismo naukowe
Introduction: The vaccine against SARS-CoV-2 provides humoral immunity to fight COVID-19; however, the acquired immunity gradually declines. Booster vaccination restores reduced humoral immunity; however, its effect on newly emerging variants, such as the Omicron variant, is a concern. As the waves of COVID-19 cases and vaccine programs differ between countries, it is necessary to know the domestic effect of the booster.
Methods: Serum samples were obtained from healthcare workers (20-69 years old) in the Pfizer BNT162b2 vaccine program at the Toyama University Hospital 6 months after the second dose (6mA2D, n = 648) and 2 weeks after the third dose (2wA3D, n = 565). The anti-SARS-CoV-2 antibody level was measured, and neutralization against the wild-type and variants (Delta and Omicron) was evaluated using pseudotyped viruses. Data on booster-related events were collected using questionnaires.
Results: The median anti-SARS-CoV-2 antibody was >30.9-fold elevated after the booster (6mA2D, 710.0 U/mL [interquartile range (IQR): 443.0-1068.0 U/mL]; 2wA3D, 21927 U/mL [IQR: 15321.0->25000.0 U/mL]). Median neutralizing activity using 100-fold sera against wild-type-, Delta-, and Omicron-derived variants was elevated from 84.6%, 36.2%, and 31.2% at 6mA2D to >99.9%, 99.1%, and 94.6% at 2wA3D, respectively. The anti-SARS-CoV-2 antibody levels were significantly elevated in individuals with fever ≥37.5 °C, general fatigue, and myalgia, local swelling, and local hardness.
Conclusion: The booster effect, especially against the Omicron variant, was observed in the Japanese population. These findings contribute to the precise understanding of the efficacy and side effects of the booster and the promotion of vaccine campaigns.
(Copyright © 2022 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.)

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