Evidence map›Paper›PMID 25458968›Full record

ReviewCytokine2015

T cell subsets and their signature cytokines in autoimmune and inflammatory diseases.

Itay Raphael, Saisha Nalawade, Todd N Eagar, Thomas G Forsthuber

Abstract readReview
In one paragraph

Review in Cytokine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 604 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
604citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

604 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. A Comprehensive Review of Kimura Disease.Head and neck pathology · 2025
    Pooled it
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  9. Sex Steroid Hormone Regulation of T-Cell Function and Antitumor Immunity.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Review
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  18. A distinct TCRiScience · 2026
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544 more citing papers are in PubMed but not listed here.

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

4 authors.

Itay RaphaelDepartment of Biology, University of Texas at San Antonio, TX 78249, United States.
Saisha NalawadeDepartment of Biology, University of Texas at San Antonio, TX 78249, United States.
Todd N EagarDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, TX 77030, United States.
Thomas G ForsthuberDepartment of Biology, University of Texas at San Antonio, TX 78249, United States. Electronic address: Thomas.forsthuber@utsa.edu.

Funding

RCMI Center for Interdiscplinary Health Research CIHRG12MD007591 · NIMHD · UNIVERSITY OF TEXAS SAN ANTONIO · PI PERRY, GEORGE · 2012 to 2016
$10.4M
Modulating B and T cell functions in EAE through gamma secretase and NotchR01NS081237 · NINDS · METHODIST HOSPITAL RESEARCH INSTITUTE · PI EAGAR, TODD N · 2013 to 2017
$1.4M
Steroid resistance: Experimental Autoimmune Encephalomyelitis/Multiple SclerosisR01NS052177 · NINDS · UNIVERSITY OF TEXAS SAN ANTONIO · PI FORSTHUBER, THOMAS G. · 2007 to 2010
$1.2M
MIF inhibition as a novel treatment for autoimmune myocarditisR21AI110771 · NIAID · UNIVERSITY OF TEXAS SAN ANTONIO · PI FORSTHUBER, THOMAS G. · 2014 to 2015
$404k
NIAID NIH HHS R21 AI110771NIMHD NIH HHS G12 MD007591NIMHD NIH HHS G12MD007591NINDS NIH HHS NS081237NINDS NIH HHS NS52177NINDS NIH HHS R01 NS052177NINDS NIH HHS R01 NS081237
6 · The paper itself

Abstract

CD4(+) T helper (Th) cells are critical for proper immune cell homeostasis and host defense, but are also major contributors to pathology of autoimmune and inflammatory diseases. Since the discovery of the Th1/Th2 dichotomy, many additional Th subsets were discovered, each with a unique cytokine profile, functional properties, and presumed role in autoimmune tissue pathology. This includes Th1, Th2, Th17, Th22, Th9, and Treg cells which are characterized by specific cytokine profiles. Cytokines produced by these Th subsets play a critical role in immune cell differentiation, effector subset commitment, and in directing the effector response. Cytokines are often categorized into proinflammatory and anti-inflammatory cytokines and linked to Th subsets expressing them. This article reviews the different Th subsets in terms of cytokine profiles, how these cytokines influence and shape the immune response, and their relative roles in promoting pathology in autoimmune and inflammatory diseases. Furthermore, we will discuss whether Th cell pathogenicity can be defined solely based on their cytokine profiles and whether rigid definition of a Th cell subset by its cytokine profile is helpful.

Indexed as

Autoimmune DiseasesCD4-Positive T-LymphocytesCytokinesHumansInflammationMultiple SclerosisTh17 CellsTh1 CellsTh2 CellsT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsCytokinesAutoimmune diseaseExperimental autoimmune encephalomyelitisMultiple sclerosisSignature cytokineT cell subset

Identifiers

PMID25458968
PMCPMC4416069

What OpenQuestion holds

Textmetadata
LicenceTDM
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.