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Peer-reviewed Lead author Corresponding author International journal
Jul 30, 2021

Correlates of Neutralizing/SARS-CoV-2-S1-binding Antibody Response with Adverse Effects and Immune Kinetics in BNT162b2-Vaccinated Individuals.

medRxiv : the preprint server for health sciences
  • Kenji Maeda
  • Masayuki Amano
  • Yukari Uemura
  • Kiyoto Tsuchiya
  • Tomoko Matsushima
  • Kenta Noda
  • Yosuke Shimizu
  • Asuka Fujiwara
  • Yuki Takamatsu
  • Yasuko Ichikawa
  • Hidehiro Nishimura
  • Mari Kinoshita
  • Shota Matsumoto
  • Hiroyuki Gatanaga
  • Kazuhisa Yoshimura
  • Shin-Ichi Oka
  • Ayako Mikami
  • Wataru Sugiura
  • Toshiyuki Sato
  • Tomokazu Yoshida
  • Shinya Shimada
  • Hiroaki Mitsuya
  • Display all

Volume
11
Number
1
First page
22848
Last page
22848
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1101/2021.07.27.21261237

While mRNA vaccines against SARS-CoV-2 are exceedingly effective in preventing symptomatic infection, their immune response features remain to be clarified. In the present prospective study, 225 healthy individuals in Japan, who received two BNT162b2 doses, were enrolled. Correlates of BNT162b2-elicited SARS-CoV-2-neutralizing activity (50% neutralization titer: NT50; assessed using infectious virions) with various determinants were examined and the potency of sera against variants of concerns was determined. Significant rise in NT50s was seen in sera on day 28 post-1st dose. A moderate inverse correlation was seen between NT50s and ages, but no correlation seen between NT50s and adverse effects. NT50s and SARS-CoV-2-S1-binding-IgG levels on day 28 post-1st dose and pain scores following the 2nd dose were greater in women than in men. The average half-life of NT50s was ~ 68 days, and 23.6% (49 out of 208 individuals) failed to show detectable neutralizing activity on day 150. While sera from elite-responders (NT50s > 1,500: the top 4% among the participants) potently to moderately blocked all variants of concerns examined, some sera with low NT50s failed to block the B.1.351-beta strain. Since BNT162b2-elicited immunity against SARS-CoV-2 is short, an additional vaccine or other protective measures are needed.

Link information
DOI
https://doi.org/10.1101/2021.07.27.21261237
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/34373860
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8351777
ID information
  • DOI : 10.1101/2021.07.27.21261237
  • Pubmed ID : 34373860
  • Pubmed Central ID : PMC8351777

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