Evidence map›Paper›PMID 41803911›Full record

ArticleBMC medicine2026

Kinetics of antibodies and risk of respiratory syncytial virus infection: a longitudinal cohort in Taizhou City, eastern China.

Qiang Wang, David Hodgson, Bo Zheng, Hongbiao Liang, Suyi Zhang, Jiahao Xu, Kathy Leung, Adam Kucharski, Haijiang Lin, Weibing Wang

Abstract read
In one paragraph

Article in BMC medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Qiang Wang *Shanghai Institute of Infectious Disease and Biosecurity, School of Public Health, Fudan University, Shanghai, China.
David Hodgson *Center of Mathematical Modelling of Infectious Diseases, London, School of Hygiene & Tropical Medicine , London, UK.
Bo Zheng *Key Laboratory of Public Health Safety of Ministry of Education, Fudan University, Shanghai, China.
Hongbiao LiangTaizhou City Center for Disease Control and Prevention, Zhejiang Province, Taizhou, China.
Suyi ZhangShanghai Institute of Infectious Disease and Biosecurity, School of Public Health, Fudan University, Shanghai, China.
Jiahao XuTaizhou City Center for Disease Control and Prevention, Zhejiang Province, Taizhou, China.
Kathy LeungWHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
Adam KucharskiCenter of Mathematical Modelling of Infectious Diseases, London, School of Hygiene & Tropical Medicine , London, UK.
Haijiang LinTaizhou City Center for Disease Control and Prevention, Zhejiang Province, Taizhou, China. fudanlhj@qq.com.
Weibing WangShanghai Institute of Infectious Disease and Biosecurity, School of Public Health, Fudan University, Shanghai, China. wwb@fudan.edu.cn.

Funding

China Postdoctoral Science Foundation 2024M750555General Research Fund of the Research Grant Council of Hong Kong 17111524National Natural Science Foundation of China 82073612Postdoctoral Fellowship Program (Grade C) of China Postdoctoral Science Foundation GZC20230467Shanghai Jiading District High-Quality Development Key Discipline of Infectious Disease Epidemiology GWGZLXK-2023-01Shanghai Municipal Science and Technology Major Project ZD2021CY001Shanghai New Three-year Action Plan for Public Health GWVI-11.1-03Shanghai Post-doctoral Excellence Program 2024084Special Support Program for High Level Talents in Taizhou City TZ2022-2
6 · The paper itself

Abstract

backgroundRespiratory syncytial virus (RSV) causes recurrent infections throughout life. Yet, the form and durability of antibody-mediated protection induced by infection remained poorly understood.

methodsWe conducted a longitudinal cohort study in Taizhou City, China. Participant age distribution approximately reflected the age structure of population in Taizhou. Blood samples were collected at baseline (March 12, 2023) and four follow-up visits (May 7-26, 2023, August 13-23, 2023, November 12, 2023, and June 2-3, 2024). Serum-specific RSV pre-fusion F (PreF) protein antibody titres were measured for all samples, and neutralising antibodies against RSV strain A2 and RSV strain B were assessed in a subset. Using a Bayesian inference framework and reversible-jump Markov Chain Monte Carlo, we recovered individual infection histories, estimated population-level RSV incidence, and characterised antibody dynamics from longitudinal PreF titres. We also estimated the correlates of protection (COP) by quantifying the relationship between PreF antibody titres and infection risk.

resultsA total of 508 individuals were included. Over the study period, two RSV epidemic waves were observed: the first wave between May and November 2023 and the second from February to May 2024. We estimated seasonal RSV infection rates of 4-7% in the community-based population. Post-infection immunity responses were most robust in young children ≤ 5 years and weakest in adults ≥ 75 years, with peak fold rises in antibody titres of 29.4 and 5.4, respectively. The post-infection antibody titres declined substantially, with fourfold rises sustained for an average of 128 days (95% credible interval of 21-281). The probability of protection given exposure increased with higher PreF titres across all age groups. However, the predictive performance of PreF titres as a COP varied markedly by age: titres strongly predicted protection in young children but showed weaker discrimination in older children and adults, and minimal predictive value in the oldest adults.

conclusionsThese results revealed age-related differences in the durability and protective value of natural infection-elicited RSV PreF antibody responses, emphasising the importance of age-specific prevention strategies.

Indexed as

Antibodies, ViralRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsAdolescentAdultAgedAntibodies, NeutralizingChildChild, PreschoolChinaFemaleHumansIncidenceInfantLongitudinal StudiesMaleAntibodies, NeutralizingAntibodies, ViralLongitudinal cohortModellingRespiratory syncytial virusSeroepidemiology

Identifiers

PMID41803911
PMCPMC13085770

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.