Evidence map›Paper›PMID 23405897›Full record

ReviewImmunological reviews2013

The Th17 family: flexibility follows function.

Rajatava Basu, Robin D Hatton, Casey T Weaver

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed, 1 pooled it
15.1field-weighted citation impact, top 1% 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

130 citing papers in PubMed, 1 synthesis or guideline pooled it, 228 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Effect of theHeliyon · 2024
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Frontiers in immunology · 2023
    Article
  12. RORγt expression in mature TScience advances · 2022
    Article
  13. Article
  14. Review
  15. RORγt-Expressing Pathogenic CD4Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  16. Article
  17. The Relationship between Cancer and Paraoxonase 1.Antioxidants (Basel, Switzerland) · 2022
    Review
  18. Review
  19. Review
  20. Review

70 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

3 authors at 1 institution in 1 country.

Rajatava BasuDepartment of Pathology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. rbasu@uab.edu
Robin D Hatton
Casey T Weaver
University of Alabama at Birmingham · US

Funding

INNATE AND ADAPTIVE MICROBIAL IMMUNITY IN IBDP01DK071176 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ELSON, CHARLES O · 2005 to 2014
$12.5M
Mucosal HIV and Immunobiology CenterR24DK064400 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SMITH, PHILLIP D · 2003 to 2012
$4.8M
Factors Controlling Effector T Cell Maintenance in the Pathogenesis of ColitisR01DK093015 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WEAVER, CASEY T · 2011 to 2015
$1.6M
Control of chromatin landscapes in effector T cell lineage specificationsR01AI077574 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WEAVER, CASEY T · 2009 to 2012
$1.5M
NIAID NIH HHS R01 AI077574NIDDK NIH HHS P01 DK071176NIDDK NIH HHS R01 DK093015NIDDK NIH HHS R24 DK064400
6 · The paper itself

Abstract

Discovery of the T-helper 17 (Th17) subset heralded a major shift in T-cell biology and immune regulation. In addition to defining a new arm of the adaptive immune response, studies of the Th17 pathway have led to a greater appreciation of the developmental flexibility, or plasticity, that is a feature of T-cell developmental programs. Since the initial finding that differentiation of Th17 cells is promoted by transforming growth factor-β (TGFβ), it became clear that Th17 cell development overlapped that of induced regulatory T (iTreg) cells. Subsequent findings established that Th17 cells are also unusually flexible in their late developmental programming, demonstrating substantial overlap with conventional Th1 cells through mechanisms that are just beginning to be understood but would appear to have important implications for immunoregulation at homeostasis and in immune-mediated diseases. Herein we examine the developmental and functional features of Th17 cells in relation to iTreg cells, Th1 cells, and Th22 cells, as a basis for understanding the contributions of this pathway to host defense, immune homeostasis, and immune-mediated disease.

Indexed as

Cell DifferentiationForkhead Transcription FactorsGene Expression RegulationHomeostasisHumansInterferon-gammaInterleukin-12Interleukin-17Nuclear Receptor Subfamily 1, Group F, Member 3Signal TransductionTh17 CellsTh1 CellsT-Lymphocytes, RegulatoryTransforming Growth Factor betaForkhead Transcription FactorsFOXP3 protein, humanInterferon-gammaInterleukin-12Interleukin-17Nuclear Receptor Subfamily 1, Group F, Member 3RORC protein, humanTransforming Growth Factor beta

Identifiers

PMID23405897
PMCPMC3607325
OpenAlexW2054627147

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.