Evidence map›Paper›PMID 18613831›Full record

ReviewImmunological reviews2008

Th17 cells in human disease.

Laura A Tesmer, Steven K Lundy, Sujata Sarkar, David A Fox

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Immunological reviews, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03615729 (RORC Genetic Polymorphism and Serum Levels in Patients With Rheumatoid Arthritis), which is not on this map. Cited by 546 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
546citing papers in PubMed, 4 pooled it
25.6field-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.

NCT03615729 completednot on this mapstarted 2016, after this paper: background citation

RORC Genetic Polymorphism and Serum Levels in Patients With Rheumatoid Arthritis

TypeobservationalSponsorAssiut UniversityRan2016 to 2018Enrolled89ConditionsGenetic Predisposition to Disease
3 · Its place in the literature

Who cites it

546 citing papers in PubMed, 4 syntheses or guidelines pooled it, 1,090 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Behçet's Disease: A Comprehensive Review on the Role ofInternational journal of molecular sciences · 2023
    Pooled it
  5. Trial
  6. Trial
  7. Neutrophils in cancer.Nature reviews. Cancer · 2026
    Review
  8. Article
  9. Comparison of plasma cytokine expression in adult haematological malignancy patients with bacterial and/or fungal infections.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Correlation between IL-17 levels and chronic urticaria: Systematic review and meta-analysis.The journal of allergy and clinical immunology. Global · 2026
    Article
  14. Dissecting PGENature communications · 2026
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review

486 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 at 2 institutions in 1 country.

Laura A TesmerDepartment of Internal Medicine, Division of Rheumatology, Rheumatic Disease Core Center, University of Michigan, Ann Arbor, MI 48109-5358, USA.
Steven K Lundy
Sujata Sarkar
David A Fox
Michigan Medicine · USUniversity of Arizona · US

Funding

Regulation of Antigen-Specific T Cells and Arthrites Inflammation by B CellsK01AR053846 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUNDY, STEVEN K. · 2007 to 2011
$558k
NIAMS NIH HHS K01 AR053846
6 · The paper itself

Abstract

summaryOur understanding of the role of T cells in human disease is undergoing revision as a result of the discovery of T-helper 17 (Th17) cells, a unique CD4(+) T-cell subset characterized by production of interleukin-17 (IL-17). IL-17 is a highly inflammatory cytokine with robust effects on stromal cells in many tissues. Recent data in humans and mice suggest that Th17 cells play an important role in the pathogenesis of a diverse group of immune-mediated diseases, including psoriasis, rheumatoid arthritis, multiple sclerosis, inflammatory bowel disease, and asthma. Initial reports also propose a role for Th17 cells in tumorigenesis and transplant rejection. Important differences, as well as many similarities, are emerging when the biology of Th17 cells in the mouse is compared with corresponding phenomena in humans. As our understanding of human Th17 biology grows, the mechanisms underlying many diseases are becoming more apparent, resulting in a new appreciation for both previously known and more recently discovered cytokines, chemokines, and feedback mechanisms. Given the strong association between excessive Th17 activity and human disease, new therapeutic approaches targeting Th17 cells are highly promising, but the potential safety of such treatments may be limited by the role of these cells in normal host defenses against infection.

Indexed as

AnimalsCD4-Positive T-LymphocytesGraft RejectionGram-Positive Bacterial InfectionsHumansImmune System DiseasesInterleukin-17MiceMycosesNeoplasmsReceptors, Pattern RecognitionT-Lymphocyte SubsetsVirus DiseasesInterleukin-17Receptors, Pattern Recognition

Identifiers

PMID18613831
PMCPMC3299089
OpenAlexW2017987372

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.