Evidence map›Paper›PMID 41350702›Full record

Observational studyBMC public health2025

WSK-V102C COVID-19 vaccine effectiveness against SARS-CoV-2 JN.1 symptomatic infection among adults 60 years and older: a prospective observational cohort study in Shaanxi Province, China, 2024.

Lin Tang, Weijun Hu, Yajun Li, Chunyan Guo, Zhaojie Feng, Ningpei Bai, Ruize Wang, Shaobai Zhang, Yuelei Wang, Siyu Liu and 6 more

Abstract readObservational Study
In one paragraph

Observational study in BMC public health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Lin Tang *National Immunization Programme, Chinese Center for Disease Control and Prevention, Beijing, China.
Weijun Hu *Shaanxi Provincial Center for Disease Control and Prevention, Xi'an, China.
Yajun LiShaanxi Provincial Center for Disease Control and Prevention, Xi'an, China.
Chunyan GuoXixian New Area Center for Public Health Management, Xi'an, China.
Zhaojie FengXixian New Area Center for Public Health Management, Xi'an, China.
Ningpei BaiChongqing Municipal Center for Disease Control and Prevention, Chongqing, China.
Ruize WangShaanxi Provincial Center for Disease Control and Prevention, Xi'an, China.
Shaobai ZhangShaanxi Provincial Bureau of Disease Control and Prevention, Xi'an, China.
Yuelei WangXi'an Municipal Center for Disease Control and Prevention, Xi'an, China.
Siyu LiuNational Immunization Programme, Chinese Center for Disease Control and Prevention, Beijing, China.
Xiaoqi WangNational Immunization Programme, Chinese Center for Disease Control and Prevention, Beijing, China.
Qianqian LiuNational Immunization Programme, Chinese Center for Disease Control and Prevention, Beijing, China.
Xiaoxue LiuNational Immunization Programme, Chinese Center for Disease Control and Prevention, Beijing, China.
Lance E RodewaldNational Immunization Programme, Chinese Center for Disease Control and Prevention, Beijing, China.
Fuzhen WangNational Immunization Programme, Chinese Center for Disease Control and Prevention, Beijing, China. wangfz@chinacdc.cn.
Zundong YinNational Immunization Programme, Chinese Center for Disease Control and Prevention, Beijing, China. yinzd@chinacdc.cn.

Funding

This work was supported by the Emergency Key Program of Guangzhou Laboratory, project Evaluation of Effectiveness of COVID-19 Vaccine against SARS-CoV-2 Outbreak in China. SRPG22-009
6 · The paper itself

Abstract

backgroundWSK-V102C is a trimeric recombinant protein COVID-19 vaccine against XBB1.5/BA.5/Delta variants that was approved for emergency use in China in June 2023. We evaluated WSK-V102C vaccine effectiveness (VE) against SARS CoV-2 JN.1 symptomatic infection among adults aged ≥ 60 years using an observational prospective cohort study.

methodsParticipants were recruited in Xixian New Area, Shaanxi Province in December 2023 and January 2024 and were offered the choice of vaccination or no vaccination. Vaccination was defined by receipt of one dose of WSK-V102C vaccine; follow-up was active, involving periodic PCR testing for infection - weekly for three months and every two weeks until the six-to-seven month follow-up was completed. The primary outcome of interest was laboratory-proven symptomatic SARS-CoV-2 infection. Cox proportional hazards regression modelling was used to estimate adjusted hazard ratios (aHR) for estimation of adjusted vaccine effectiveness (aVE), calculated as (1 - adjusted hazard ratio) multiplied by 100%, with 95% confidence intervals (CIs).

resultsAmong 6 313 participants meeting inclusion criteria, 3 216 received WSK-V102C and 3 097 did not receive WSK-V102C (or other COVID-19 vaccine) during the study period. The mean (SD) age of participants was 69.6 (6.4) years; the median follow-up time was 160 (IQR 153-166) days; 140 (2.2%) participants tested positive for SARS-CoV-2 nucleic acid, with 63 having symptomatic infection. No infected subjects were hospitalized or died. For prevention of symptomatic SARS-CoV-2 infection, all-ages aVE was 42.0% (95%CI: 3.5%, 65.1%); in 60-74-year-olds aVE was 50.1% (95%CI: 8.8%, 72.7%); and in individuals 75 years old and above, aVE was 10.6% (95%CI: -139.0%, 66.6%). Duration of symptoms was longer in unvaccinated subjects. Rates of laboratory-proven infection, including asymptomatic infection, were not different by vaccination status.

conclusionsAmong individuals aged ≥ 60 years, WSK-V102C vaccination provided moderate protection against JN.1 symptomatic infection within 6 months, suggesting that older people can benefit from use of this vaccine.

Indexed as

COVID-19COVID-19 VaccinesVaccine EfficacyAgedChinaFemaleHumansMaleMiddle AgedProspective StudiesSARS-CoV-2COVID-19 VaccinesCohort studyCOVID-19Real-world studyRecombinant protein vaccineSARS-CoV-2Vaccine effectiveness

Identifiers

PMID41350702
PMCPMC12797716

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

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 Socratic graph.