Evidence map›Paper›PMID 26865046›Full record

ArticleScientific reports2016

Circulating memory T follicular helper subsets, Tfh2 and Tfh17, participate in the pathogenesis of Guillain-Barré syndrome.

Yuanyuan Che, Jinpeng Qiu, Tao Jin, Fei Yin, Man Li, Yanfang Jiang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 51 citations in OpenAlex.

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  12. Imbalance of circulating CTLA4Clinical and experimental medicine · 2022
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  18. Review
  19. Follicular helper T cell and memory B cell immunity in CHC patients.Journal of molecular medicine (Berlin, Germany) · 2019
    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

6 authors at 3 institutions in 1 country.

Yuanyuan CheGenetic Diagnosis Center, The First Hospital of Jilin University, Changchun 130021, China.
Jinpeng QiuGenetic Diagnosis Center, The First Hospital of Jilin University, Changchun 130021, China.
Tao JinGenetic Diagnosis Center, The First Hospital of Jilin University, Changchun 130021, China.
Fei YinDepartment of Neurology, The Second Hospital of Jilin University, Changchun 130021, China.
Man LiGenetic Diagnosis Center, The First Hospital of Jilin University, Changchun 130021, China.
Yanfang JiangGenetic Diagnosis Center, The First Hospital of Jilin University, Changchun 130021, China.
First Hospital of Jilin University · CNJilin University · CNSecond Affiliated Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating memory T follicular helper subsets, Tfh2 and Tfh17 are found to be aberrantly regulated in many autoimmune diseases. However, their roles in the pathogenesis of GBS are still unclear. This study examined the phenotype, distribution, clinical relevance and potential function of Tfh2 and Tfh17 in 36 GBS patients (including 24 AMAN and 12 AIDP patients). We found that the absolute counts of total memory Tfh cells were significantly increased in AMAN, while no significant difference in AIDP compared with HC. Furthermore, the levels of the three subsets of memory Tfh cells, Tfh1, Tfh2 and Tfh17, were differentially altered in AMAN. The absolute counts of Tfh1, Tfh2 and Tfh17 were all increased to a higher level in AMAN. The ratio of (Tfh2+Tfh17)/Tfh1 and the percentages of ICOS(+) cells in Tfh2 and Tfh17 cells were greater in AMAN when compared to AIDP and HC, and the former had a positive correlation with the severity of both AMAN and AIDP. Conversely, the percentages of PD1(+) cells in Tfh2 and Tfh17 cells were lower in AMAN than in HC. Therefore, circulating memory Tfh2 and Tfh17 cells might promote the autoantibody-related immune response and serve as useful markers to evaluate the progression of AMAN.

Indexed as

Immunologic MemoryAdultAgedAutoantibodiesCase-Control StudiesDisease ProgressionFemaleGene ExpressionGuillain-Barre SyndromeHumansImmunophenotypingInducible T-Cell Co-Stimulator ProteinLymphocyte CountMaleMiddle AgedPhenotypeAutoantibodiesICOS protein, humanInducible T-Cell Co-Stimulator ProteinPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID26865046
PMCPMC4750093
OpenAlexW2258373086

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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.