Evidence map›Paper›PMID 42136676›Full record

ArticleFrontiers in immunology2026

Hepatitis B vaccination in Chinese infants (2002-2006, Guangdong): long-term effectiveness in adulthood and biological features of HBV infection.

Qiao Liao, Bochao Liu, Fenfang Liao, Ru Xu, Min Wang, Zhengang Shan, Jieting Huang, HuiShan Zhong, Yongshui Fu, Huaqin Liang and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. 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

11 authors.

Qiao Liao *Institute of Blood Transfusion and Hematology, Guangzhou Blood Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
Bochao Liu *Institute of Blood Transfusion and Hematology, Guangzhou Blood Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
Fenfang Liao *Institute of Blood Transfusion and Hematology, Guangzhou Blood Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
Ru XuInstitute of Blood Transfusion and Hematology, Guangzhou Blood Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
Min WangInstitute of Blood Transfusion and Hematology, Guangzhou Blood Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
Zhengang ShanInstitute of Blood Transfusion and Hematology, Guangzhou Blood Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
Jieting HuangInstitute of Blood Transfusion and Hematology, Guangzhou Blood Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
HuiShan ZhongInstitute of Blood Transfusion and Hematology, Guangzhou Blood Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
Yongshui FuDepartment of Hematology, School of Medicine, The Second Affiliated Hospital of South China University of Technology (Guangzhou First People's Hospital), Guangzhou, Guangdong, China.
Huaqin LiangInstitute of Blood Transfusion and Hematology, Guangzhou Blood Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
Xia RongInstitute of Blood Transfusion and Hematology, Guangzhou Blood Center, Guangzhou Medical University, Guangzhou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hepatitis B virus infection is a serious health concern in China. The National Immunization Program has implemented universal hepatitis B vaccination for infants for over two decades. The serological characteristics of hepatitis B virus and the causes of infections among adult blood donors born after 2002 remain undetermined. Methods: Qualified blood donors born between 2002 and 2006 from Guangdong were screened for antibodies against hepatitis B surface antigen (anti-HBs) and hepatitis B core antigen (anti-HBc). Donations positive for HBsAg were subjected to various tests, including HBV serological markers, quantitative PCR (qPCR), and nested PCR, to further analyze the molecular characteristics of HBV DNA. Notable mutations were identified through comparison with HBV reference sequences obtained from blood donors. Results: This study enrolled 5,487 blood donors with complete results for anti-HBs and anti-HBc testing. Overall, the prevalence of anti-HBs was 47.73% in males and 46.16% in females, while the prevalence of anti-HBc was 10.58% in males and 12.79% in females. Among blood donors born between 2002 and 2006, the prevalence of anti-HBs declined progressively with more recent birth years, decreasing from 54.55% to 40.23%, while the prevalence of anti-HBc remained relatively stable at around 11%. The prevalence (56.54%) and level of anti-HBs in the Pearl River Delta were significantly higher than those in the eastern, western, and northern regions of Guangdong (P<0.001). Quantitative analysis revealed that anti-HBs levels were significantly higher in the anti-HBc+ cohort than in the anti-HBc- group. Furthermore, whole genome sequences genotyping of 72 HBsAg+ samples revealed that 75% (54/72) were genotype B and 25% (18/72) were genotype C. Nine HBV-related point mutations were detected, including four previously reported variants and five novel substitutions. Additionally, six insertions/deletions were observed in genotype B/C. All these mutations were mapped to critical functional regions within the PreS1, Core, X, and S genes. Conclusion: Only 47.13% of young adults vaccinated at birth under the national immunization program retained protective antibodies at the time of testing, indicating this age group vulnerable to HBV infection. This decline has consequently increased the risk of breakthrough infection, necessitating booster vaccination among young adults in Guangdong.

Indexed as

Hepatitis BHepatitis B VaccinesHepatitis B virusAdultBlood DonorsChinaDNA, ViralEast Asian PeopleFemaleHepatitis B AntibodiesHepatitis B Core AntigensHepatitis B Surface AntigensHumansInfantMaleVaccinationDNA, ViralHepatitis B AntibodiesHepatitis B Core AntigensHepatitis B Surface AntigensHepatitis B Vaccinesanti-HBcanti-HBsblood donorgene mutationsvaccination

Identifiers

PMID42136676
PMCPMC13167707

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.