Evidence map›Paper›PMID 35254403›Full record

ArticleThe Journal of experimental medicine2022

Monocytic MDSCs homing to thymus contribute to age-related CD8+ T cell tolerance of HBV.

Zhong Fang, Yi Zhang, Zhaoqin Zhu, Cong Wang, Yao Hu, Xiuhua Peng, Dandan Zhang, Jun Zhao, Bisheng Shi, Zhongliang Shen and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.8field-weighted citation impact, top 4% of its field
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

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Observational
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  8. Potential role of liver-resident CD3JHEP reports : innovation in hepatology · 2025
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  13. [Immune status of inactive HBsAg antigen carriers with chronic HBV infection].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2024
    Article
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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

22 authors at 3 institutions in 2 countries.

Zhong FangKey Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0002-7703-8686
Yi ZhangShanghai Public Health Clinical Center, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0002-2383-4126
Zhaoqin ZhuShanghai Public Health Clinical Center, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0003-1101-5999
Cong WangKey Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0001-6684-6891
Yao HuDepartment of Infectious Diseases, Children's Hospital of Fudan University, Shanghai, China.ORCID 0000-0001-5175-6164
Xiuhua PengShanghai Public Health Clinical Center, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0001-8442-2005
Dandan ZhangShanghai Public Health Clinical Center, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0002-2627-9295
Jun ZhaoShanghai Public Health Clinical Center, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0001-9333-1471
Bisheng ShiKey Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0002-4740-311X
Zhongliang ShenKey Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0001-8566-9149
Min WuShanghai Public Health Clinical Center, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0002-4784-226X
Chunhua XuShanghai Public Health Clinical Center, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0003-2470-9893
Jieliang ChenKey Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0002-9647-0239
Xiaohui ZhouShanghai Public Health Clinical Center, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0001-7491-628X
Youhua XieKey Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0002-2416-7708
Hui YuDepartment of Infectious Diseases, Children's Hospital of Fudan University, Shanghai, China.ORCID 0000-0003-1342-5537
Xiaonan ZhangShanghai Public Health Clinical Center, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0002-1286-7280
Jianhua LiKey Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0001-7329-5688
Yunwen HuShanghai Public Health Clinical Center, Shanghai Medical College of Fudan University, Shanghai, China.
Maya KozlowskiKey Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0002-6550-1725
Antonio BertolettiProgram of Emerging Viral Diseases, Duke-NUS Medical School, Singapore.ORCID 0000-0002-2942-0485
Zhenghong YuanKey Laboratory of Medical Molecular Virology, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.ORCID 0000-0003-0268-4891
Shanghai Medical College of Fudan University · CNChildren's Hospital of Fudan University · CNDuke-NUS Medical School · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatitis B virus exposure in children usually develops into chronic hepatitis B (CHB). Although hepatitis B surface antigen (HBsAg)-specific CD8+ T cells contribute to resolve HBV infection, they are preferentially undetected in CHB patients. Moreover, the mechanism for this rarely detected HBsAg-specific CD8+ T cells remains unexplored. We herein found that the frequency of HBsAg-specific CD8+ T cells was inversely correlated with expansion of monocytic myeloid-derived suppressor cells (mMDSCs) in young rather than in adult CHB patients, and CCR9 was upregulated by HBsAg on mMDSCs via activation of ERK1/2 and IL-6. Sequentially, the interaction between CCL25 and CCR9 mediated thymic homing of mMDSCs, which caused the cross-presentation, transferring of peripheral HBsAg into the thymic medulla, and then promoted death of HBsAg-specific CD8+ thymocytes. In mice, adoptive transfer of mMDSCs selectively obliterated HBsAg-specific CD8+ T cells and facilitated persistence of HBV in a CCR9-dependent manner. Taken together, our results uncovered a novel mechanism for establishing specific CD8+ tolerance to HBsAg in chronic HBV infection.

Indexed as

Hepatitis B, ChronicMyeloid-Derived Suppressor CellsAnimalsCD8-Positive T-LymphocytesHepatitis B Surface AntigensHepatitis B virusHumansMiceHepatitis B Surface Antigens

Identifiers

PMID35254403
PMCPMC8906470
OpenAlexW4221015500

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.