Evidence map›Paper›PMID 41407683›Full record

Trial reportNature communications2025

Long-term protection from naturally acquired immunity against hepatitis E virus reinfection.

Xiaohui Liu, Xia Zang, Kongxin Zhu, Xingcheng Huang, Xiaowen Hu, Zhaofeng Bi, Qi Chen, Hanmin Jiang, Yijun Wang, Changlin Yang and 9 more

Abstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

19 authors.

Xiaohui Liu *State Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China.ORCID http://orcid.org/0000-0003-1828-0162
Xia Zang *Dongtai Centre for Disease Control and Prevention, Yancheng, Jiangsu, China.
Kongxin ZhuState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China.
Xingcheng HuangState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China.
Xiaowen HuState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China.
Zhaofeng BiState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China.
Qi ChenState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China.
Hanmin JiangDongtai Centre for Disease Control and Prevention, Yancheng, Jiangsu, China.
Yijun WangDongtai Centre for Disease Control and Prevention, Yancheng, Jiangsu, China.
Changlin YangDongtai Centre for Disease Control and Prevention, Yancheng, Jiangsu, China.
Donglin LiuDongtai Centre for Disease Control and Prevention, Yancheng, Jiangsu, China.
Wenhua ZhuDongtai Centre for Disease Control and Prevention, Yancheng, Jiangsu, China.
Zizheng ZhengState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China.ORCID http://orcid.org/0000-0003-0099-4212
Yingying SuState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China.
Ting WuState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China.ORCID http://orcid.org/0000-0002-1806-3056
Shoujie HuangState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China. huangshoujie@xmu.edu.cn.
Chunlan ZhuangState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China. zhuangcl@xmu.edu.cn.ORCID http://orcid.org/0000-0002-8253-2515
Jun ZhangState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China. zhangj@xmu.edu.cn.ORCID http://orcid.org/0000-0002-6601-9180
Ningshao XiaState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, Xiang'an Hospital, School of Public Health, Xiamen University, Xiamen, China.ORCID http://orcid.org/0000-0003-0179-5266

Funding

China Postdoctoral Science Foundation GZB20250195National Natural Science Foundation of China (National Science Foundation of China) 32370160National Natural Science Foundation of China (National Science Foundation of China) 823B2086Natural Science Foundation of Fujian Province (Fujian Provincial Natural Science Foundation) 2022J02005
6 · The paper itself

Abstract

The durability and protective effect of naturally acquired antibodies against hepatitis E virus (HEV) reinfection and clinical progression remain unclear in humans. In a 103-month longitudinal analysis of 7032 adult placebo recipients (aged 16 to 65 years) from a phase 3 HEV vaccine trial in China, we demonstrated that baseline anti-HEV IgG seropositivity (n = 3194) conferred over 50% higher protection against reinfection compared with seronegative individuals (n = 3838), with this protective effect remaining consistent over 8.5 years. A non-linear dose-response relationship was observed, whereby baseline anti-HEV IgG concentrations ≥0.25 WHO units/mL were associated with at least a 50% reduction in infection risk, with higher baseline antibody levels correlated with a lower risk of infection. Natural immunity provided approximately 70% protection against clinically apparent hepatitis E in the cohort, with 10 symptomatic cases identified over a decade of active surveillance. Six were hospitalized, all of whom were baseline seronegative. These findings establish that natural HEV immunity provides durable, though incomplete, protection.

Indexed as

Hepatitis AntibodiesHepatitis EHepatitis E virusReinfectionViral Hepatitis VaccinesAdolescentAdultAgedChinaFemaleHumansImmunoglobulin GLongitudinal StudiesMaleMiddle AgedYoung AdultHepatitis AntibodiesImmunoglobulin GViral Hepatitis Vaccines

Identifiers

PMID41407683
PMCPMC12711902

What Socratic holds

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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.