Evidence map›Paper›PMID 26300592›Full record

ReviewMediators of inflammation2015

Follicular Helper CD4+ T Cells in Human Neuroautoimmune Diseases and Their Animal Models.

Xueli Fan, Chenhong Lin, Jinming Han, Xinmei Jiang, Jie Zhu, Tao Jin

Open access · goldAbstract readReview
In one paragraph

Review in Mediators of inflammation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 82 citations in OpenAlex.

  1. Review
  2. Review
  3. Correlation of GABABrain and behavior · 2024
    Article
  4. The imbalance between Bregs, Tfh, and Tregs in patients with anti-N-methyl-D-aspartate receptor encephalitis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Follicular Helper CD4Mediators of inflammation · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Advances in autoimmune myasthenia gravis management.Expert review of neurotherapeutics · 2018
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Follicular T Cells from smBFrontiers in immunology · 2017
    Article
  20. Review
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

6 authors at 3 institutions in 2 countries.

Xueli FanDepartment of Neurology, The First Hospital of Jilin University, Jilin University, Changchun 130021, China.
Chenhong LinDepartment of Neurology, The First Hospital of Jilin University, Jilin University, Changchun 130021, China.
Jinming HanDepartment of Neurology, The First Hospital of Jilin University, Jilin University, Changchun 130021, China.
Xinmei JiangDepartment of Neurology, The First Hospital of Jilin University, Jilin University, Changchun 130021, China.
Jie ZhuDepartment of Neurology, The First Hospital of Jilin University, Jilin University, Changchun 130021, China ; Department of Neurobiology, Care Sciences and Society, Karolinska Institute, 14186 Stockholm, Sweden.
Tao JinDepartment of Neurology, The First Hospital of Jilin University, Jilin University, Changchun 130021, China.
First Hospital of Jilin University · CNJilin University · CNKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Follicular helper CD4(+) T (TFH) cells play a fundamental role in humoral immunity deriving from their ability to provide help for germinal center (GC) formation, B cell differentiation into plasma cells and memory cells, and antibody production in secondary lymphoid tissues. TFH cells can be identified by a combination of markers, including the chemokine receptor CXCR5, costimulatory molecules ICOS and PD-1, transcription repressor Bcl-6, and cytokine IL-21. It is difficult and impossible to get access to secondary lymphoid tissues in humans, so studies are usually performed with human peripheral blood samples as circulating counterparts of tissue TFH cells. A balance of TFH cell generation and function is critical for protective antibody response, whereas overactivation of TFH cells or overexpression of TFH-associated molecules may result in autoimmune diseases. Emerging data have shown that TFH cells and TFH-associated molecules may be involved in the pathogenesis of neuroautoimmune diseases including multiple sclerosis (MS), neuromyelitis optica (NMO)/neuromyelitis optica spectrum disorders (NMOSD), and myasthenia gravis (MG). This review summarizes the features of TFH cells, including their development, function, and roles as well as TFH-associated molecules in neuroautoimmune diseases and their animal models.

Indexed as

AnimalsAutoimmune Diseases of the Nervous SystemCD4-Positive T-LymphocytesDNA-Binding ProteinsEncephalomyelitis, Autoimmune, ExperimentalHumansInducible T-Cell Co-Stimulator ProteinInterleukin-21InterleukinsMultiple SclerosisMyasthenia GravisNeuromyelitis OpticaProto-Oncogene Proteins c-bcl-6Receptors, CXCR5BCL6 protein, humanDNA-Binding ProteinsICOS protein, humanInducible T-Cell Co-Stimulator ProteinInterleukin-21InterleukinsProto-Oncogene Proteins c-bcl-6Receptors, CXCR5

Identifiers

PMID26300592
PMCPMC4537760
OpenAlexW1891571695

What OpenQuestion holds

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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.