Neutralizing antibody responses against contemporary and future influenza A(H3N2) viruses in paradoxical clades elicited by repeated and single vaccinations

Author:

Zhang Ting1234,Han Yang23456,Huang Weijuan2,Wei Hejiang2,Zhao Yingze234,Shu Liumei7,Guo Yaxin234,Ye Beiwei234,Zhou Jianfang2,Liu Jun1234ORCID

Affiliation:

1. Collaborative Innovation Centre of Regenerative Medicine and Medical Bioresource Development and Application Co‐constructed by the Province and Ministry Guangxi Medical University Nanning China

2. National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), National Institute for Viral Disease Control and Prevention Chinese Center for Disease Control and Prevention Beijing China

3. NHC Key Laboratory of Biosafety, National Institute for Viral Disease Control and Prevention Chinese Center for Disease Control and Prevention Beijing China

4. Research Unit of Adaptive Evolution and Control of Emerging Viruses (2018RU009) Chinese Academy of Medical Sciences Beijing China

5. National Clinical Research Center for Ocular Diseases, Eye Hospital Wenzhou Medical University Wenzhou China

6. State Key Laboratory of Ophthalmology, Optometry and Visual Science, Eye Hospital Wenzhou Medical University Wenzhou China

7. Department of Health Care Beijing Daxing District Hospital Beijing China

Abstract

AbstractAs one of the most effective measures to prevent seasonal influenza viruses, annual influenza vaccination is globally recommended. Nevertheless, evidence regarding the impact of repeated vaccination to contemporary and future influenza has been inconclusive. A total of 100 subjects singly or repeatedly immunized with influenza vaccines including 3C.2a1 or 3C.3a1 A(H3N2) during 2018–2019 and 2019–2020 influenza season were recruited. We investigated neutralization antibody by microneutralization assay using four antigenically distinct A(H3N2) viruses circulating from 2018 to 2023, and tracked the dynamics of B cell receptor (BCR) repertoire for consecutive vaccinations. We found that vaccination elicited cross‐reactive antibody responses against future emerging strains. Broader neutralizing antibodies to A(H3N2) viruses and more diverse BCR repertoires were observed in the repeated vaccination. Meanwhile, a higher frequency of BCR sequences shared among the repeated‐vaccinated individuals with consistently boosting antibody response was found than those with a reduced antibody response. Our findings suggest that repeated seasonal vaccination could broaden the breadth of antibody responses, which may improve vaccine protection against future emerging viruses.

Publisher

Wiley

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