Evidence map›Paper›PMID 39775320›Full record

ArticleClinical and experimental medicine2025

The prognosis and immune repertoire characteristics of HBsAg and anti-HBs double positive chronic hepatitis B patients.

Huijun Liang, Haifang Wang, Minfeng Liang, Xiaobin Zhang, Meifen Dai, Haixia Li, Xin Li, Xiaofeng Yin, Xinyao Liu, Jiaqi Yao and 2 more

Abstract read
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Article in Clinical and experimental medicine, 2025. 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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5 · Who and what money

Authors and funding

12 authors.

Huijun Liang *The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, 528225, China.
Haifang Wang *Department of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Minfeng Liang *Department of Infectious Diseases, The First People's Hospital of Foshan, Foshan, 528000, China.
Xiaobin ZhangThe Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, 528225, China.
Meifen DaiThe Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, 528225, China.
Haixia LiDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Xin LiDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Xiaofeng YinDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Xinyao LiuDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Jiaqi YaoDepartment of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Ziyun GuanThe Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, 528225, China. lyguanzy@scut.edu.cn.
Yurong QiuGuangzhou Huayin Health Medical Group Co., Ltd, Guangzhou, 510515, China. qyr@smu.edu.cn.

Funding

Foshan science and technology plan project No. 2320001006088Guangzhou science and technology plan project No. 202102020024National Natural Science Foundation of China No. 81871712Outstanding Youths Development Scheme of Nanfang Hospital, Southern Medical University No. 2022J007
6 · The paper itself

Abstract

Coexistence of hepatitis B surface antigen (HBsAg) and hepatitis B surface antibody (anti-HBs) has been observed in some chronic hepatitis B (CHB) patients (DP patients), but the clinical outcomes and comprehensive characterization of immune micro-environmental changes for this specific population remain inconclusive. In this study, we retrospectively analyze the prognosis of 305 patients in Foshan City, Guangdong Province, China, and also investigated the molecular immunology changes in HBsAg and anti-HBs double positive CHB patients (DP group), CHB patients who had recovered from IFN-ɑ treatment (RP group), and healthy controls (HC group) using T cell receptor (TCR) and B cell receptor (BCR) immune repertoire sequencing. Our findings revealed that 22.30% of DP patients were diagnosed with severe liver disease. Immune repertoire sequencing revealed significant skewing in the diversities of T cell receptor β-chain (TRB) and immunoglobulin heavy chain (IGH) in the DP group compared to the RP group. Unique V(D)J gene combinations, such as IGHV1-18/IGHD3-22/IGHJ5, IGHV1-8/IGHD6-13/IGHJ3, and IGHV1-8/IGHD6-19/IGHJ3, as well as TRBV12-3/TRBD1/TRBJ1-5 and TRBV11-2/TRBD2/TRBJ2-1, exhibited distinct utilization patterns in the DP group. Moreover, the top ten most utilized amino acid motifs in the complementarity determining region 3 (CDR3) of TRB in the DP group showed significant differences from those in the RP group. Notably, motifs such as "xxxYDSSGYx" and "AREx" in the IGH CDR3s were selectively prevalent in the DP group. These findings are expected to provide evidence supporting the poor clinical prognosis of DP patients and offer new insights into the distinct immune micro-environmental changes of this group.

Indexed as

Hepatitis B AntibodiesHepatitis B, ChronicHepatitis B Surface AntigensAdultAgedChinaFemaleHumansImmunoglobulin Heavy ChainsMaleMiddle AgedPrognosisReceptors, Antigen, B-CellRetrospective StudiesYoung AdultHepatitis B AntibodiesHepatitis B Surface AntigensImmunoglobulin Heavy ChainsReceptors, Antigen, B-CellAnti-HBsBCRHBsAgImmune repertoireTCR

Identifiers

PMID39775320
PMCPMC11711149

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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.