Evidence map›Paper›PMID 36119056›Full record

ArticleFrontiers in immunology2022

Aberrant expansion of follicular helper T cell subsets in patients with systemic lupus erythematosus.

Xin Jin, Jia Chen, Jian Wu, Ying Lu, Baohua Li, Wenning Fu, Wei Wang, Dawei Cui

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

24 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  7. T follicular helper cells in primary immune regulatory disorders.The Journal of allergy and clinical immunology · 2025
    Review
  8. Review
  9. Review
  10. Enhancement of CD8Journal of translational autoimmunity · 2025
    Article
  11. Article
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  13. Review
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  15. Review
  16. Article
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  19. ETV5 promotes lupus pathogenesis and follicular helper T cell differentiation by inducing osteopontin expression.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  20. 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

8 authors at 4 institutions in 1 country.

Xin JinDepartment of Clinical Laboratory, Tongde Hospital of Zhejiang Province, Hangzhou, China.
Jia ChenDepartment of Nephrology Research, The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, China.
Jian WuDepartment of Clinical Laboratory, Suzhou Hospital Affiliated to Nanjing Medical University, Suzhou, China.
Ying LuDepartment of Rheumatology, Tongde Hospital of Zhejiang Province, Hangzhou, China.
Baohua LiDepartment of Clinical Laboratory, Tongde Hospital of Zhejiang Province, Hangzhou, China.
Wenning FuDepartment of Rheumatology, Tongde Hospital of Zhejiang Province, Hangzhou, China.
Wei WangDepartment of Clinical Laboratory, Tongde Hospital of Zhejiang Province, Hangzhou, China.
Dawei CuiDepartment of Blood Transfusion, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Tongde Hospital of Zhejiang Province · CNFirst Affiliated Hospital Zhejiang University · CNNanjing Medical University · CNZhejiang Chinese Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Systemic lupus erythematosus (SLE) is a chronic and complex autoimmune disease characterized by multiple autoantibodies, resulting in multiple organ and tissue damages. These pathogenic autoantibodies produced by B cells are closely correlated with follicular helper T (Tfh) cell subsets that play a fundamental role in the pathogenesis of SLE. The aim of the present study was to study the phenotype and role of circulating Tfh (cTfh) cell subsets and associated B cell subpopulations in active and inactive SLE patients. Methods: Thirty SLE outpatients and 24 healthy controls (HCs) were enrolled in this study. The frequency of cTfh cell and B cell subsets in peripheral blood mononuclear cells (PBMCs) and the plasma levels of eight cytokines were determined by flow cytometry, and plasma IL-21 levels were measured by ELISA. Meanwhile, we used MRL/lpr mice as the model of SLE to research the alterations of Tfh cells in the thymus and spleen of mice. Results: Frequencies of CD4 Conclusion: Tfh cell subsets and plasmablasts may play a fundamental role in the pathogenesis of SLE and may provide potential targets for therapeutic interventions for SLE.

Indexed as

Lupus Erythematosus, SystemicT Follicular Helper CellsAnimalsAutoantibodiesCytokinesInterleukin-6Leukocytes, MononuclearMiceMice, Inbred MRL lprT-Lymphocytes, Helper-InducerAutoantibodiesCytokinesInterleukin-6B cellsfollicular helper T cellsinterleukin-21plasmablastssystemic lupus erythematosus

Identifiers

PMID36119056
PMCPMC9478104
OpenAlexW4294176579

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.