Evidence map›Paper›PMID 27612199›Full record

ArticlePloS one2016

Production of Autoantibodies in Chronic Hepatitis B Virus Infection Is Associated with the Augmented Function of Blood CXCR5+CD4+ T Cells.

Yu Lei, Tingting Hu, Xiaofei Song, Hong Nie, Min Chen, Weixian Chen, Zhi Zhou, Dazhi Zhang, Huaidong Hu, Peng Hu and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Yu LeiDepartment of Infectious Diseases, Institute for Viral Hepatitis, Key Laboratory of Molecular Biology for Infectious Diseases, Ministry of Education, the Second Affiliated Hospital, Chongqing Medical University, No.74 Lin Jiang Rd., Yu Zhong District, 400010, Chongqing, People's Republic of China.
Tingting HuDepartment of Infectious Diseases, Institute for Viral Hepatitis, Key Laboratory of Molecular Biology for Infectious Diseases, Ministry of Education, the Second Affiliated Hospital, Chongqing Medical University, No.74 Lin Jiang Rd., Yu Zhong District, 400010, Chongqing, People's Republic of China.
Xiaofei SongDepartment of Infectious Diseases, Institute for Viral Hepatitis, Key Laboratory of Molecular Biology for Infectious Diseases, Ministry of Education, the Second Affiliated Hospital, Chongqing Medical University, No.74 Lin Jiang Rd., Yu Zhong District, 400010, Chongqing, People's Republic of China.
Hong NieDepartment of Laboratory Medicine, the Second Affiliated Hospital, Chongqing Medical University, No.74 Lin Jiang Rd., Yu Zhong District, 400010, Chongqing, People's Republic of China.
Min ChenDepartment of Infectious Diseases, Institute for Viral Hepatitis, Key Laboratory of Molecular Biology for Infectious Diseases, Ministry of Education, the Second Affiliated Hospital, Chongqing Medical University, No.74 Lin Jiang Rd., Yu Zhong District, 400010, Chongqing, People's Republic of China.
Weixian ChenDepartment of Laboratory Medicine, the Second Affiliated Hospital, Chongqing Medical University, No.74 Lin Jiang Rd., Yu Zhong District, 400010, Chongqing, People's Republic of China.
Zhi ZhouDepartment of Infectious Diseases, Institute for Viral Hepatitis, Key Laboratory of Molecular Biology for Infectious Diseases, Ministry of Education, the Second Affiliated Hospital, Chongqing Medical University, No.74 Lin Jiang Rd., Yu Zhong District, 400010, Chongqing, People's Republic of China.
Dazhi ZhangDepartment of Infectious Diseases, Institute for Viral Hepatitis, Key Laboratory of Molecular Biology for Infectious Diseases, Ministry of Education, the Second Affiliated Hospital, Chongqing Medical University, No.74 Lin Jiang Rd., Yu Zhong District, 400010, Chongqing, People's Republic of China.
Huaidong HuDepartment of Infectious Diseases, Institute for Viral Hepatitis, Key Laboratory of Molecular Biology for Infectious Diseases, Ministry of Education, the Second Affiliated Hospital, Chongqing Medical University, No.74 Lin Jiang Rd., Yu Zhong District, 400010, Chongqing, People's Republic of China.
Peng HuDepartment of Infectious Diseases, Institute for Viral Hepatitis, Key Laboratory of Molecular Biology for Infectious Diseases, Ministry of Education, the Second Affiliated Hospital, Chongqing Medical University, No.74 Lin Jiang Rd., Yu Zhong District, 400010, Chongqing, People's Republic of China.
Hong RenDepartment of Infectious Diseases, Institute for Viral Hepatitis, Key Laboratory of Molecular Biology for Infectious Diseases, Ministry of Education, the Second Affiliated Hospital, Chongqing Medical University, No.74 Lin Jiang Rd., Yu Zhong District, 400010, Chongqing, People's Republic of China.
Chongqing Medical University · CNDalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T follicular helper cells (Tfh) provide help to B cells to support their activation, expansion and differentiation. However, the role of Tfh cells in chronic HBV infection is poorly defined. The aim of this research was to examine the function of Tfh cells and whether they are involved in HBV related disease. Blood CXCR5+CD4+T cells and B cells in 85 patients with chronic HBV infection (HBV patients) and health controls (HC) were examined by flow cytometry. The molecule expression in blood CXCR5+CD4+ T cells was detected by real-time PCR. Blood CXCR5+CD4+ T cells and B cells were co-cultured and the production of Ig and cytokines was detected by ELISA. Autoantibodies were detected by indirect immunofluorescence and immunospot assay. We found that blood CXCR5+CD4+ T cells in patients with chronic HBV infection (HBV patients) expressed higher level of activation related molecules and cytokines than that from health controls (HC).In HBV patients, the frequency of blood CXCR5+CD4+ T cells was significantly correlated with serum ALT and AST. We also found that blood CXCR5+CD4+ T cells from HBV patients could induce B cells to secret higher level of immunoglobulin than that from HC. Several autoantibodies, including ANA, ss-A, ss-B, Scl-70, Jo-1, ect, were indeed positive in 65% HBV patients. Among HBV patients, expression of function related molecules was significantly higher in blood CXCR5+CD4+ T cells from patients with autoantibodies than that without autoantibodies. Our research indicated that blood CXCR5+CD4+ T cells from HBV patients were over activated and show augmented capacity to help B cells for antibody secreting, which might correlated with liver inflammation and the production of autoantibodies in extrahepatic manifestations.

Indexed as

AdultAutoantibodiesB-LymphocytesCD4 Lymphocyte CountCD4-Positive T-LymphocytesFemaleHepatitis B, ChronicHumansImmunophenotypingMaleReceptors, CXCR5AutoantibodiesReceptors, CXCR5

Identifiers

PMID27612199
PMCPMC5017876
OpenAlexW2516178404

What OpenQuestion holds

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Registered trials

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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.