Evidence map›Paper›PMID 22177921›Full record

ArticleImmunity2011

Th17 cells are long lived and retain a stem cell-like molecular signature.

Pawel Muranski, Zachary A Borman, Sid P Kerkar, Christopher A Klebanoff, Yun Ji, Luis Sanchez-Perez, Madhusudhanan Sukumar, Robert N Reger, Zhiya Yu, Steven J Kern and 12 more

Abstract read
In one paragraph

Article in Immunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 293 papers.

0numbers the graph read from it
0cells of the map it votes in
293citing papers in PubMed
–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

293 citing papers in PubMed.

  1. Trial
  2. Contextualizing TNature reviews. Immunology · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Th17 cell pathogenicity in autoimmune disease.Experimental & molecular medicine · 2025
    Review
  8. Article
  9. Review
  10. A New Method of Canine CD4International journal of molecular sciences · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

233 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Pawel MuranskiNational Cancer Institute, Bethesda, MD 20892, USA.
Zachary A Borman
Sid P Kerkar
Christopher A Klebanoff
Yun Ji
Luis Sanchez-Perez
Madhusudhanan Sukumar
Robert N Reger
Zhiya Yu
Steven J Kern
Rahul Roychoudhuri
Gabriela A Ferreyra
Wei Shen
Scott K Durum
Lionel Feigenbaum
Douglas C Palmer
Paul A Antony
Chi-Chao Chan
Arian Laurence
Robert L Danner
Luca Gattinoni
Nicholas P Restifo

Funding

Building on the success of the adoptive immunotherapy of cancerZIABC010763 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ROSENBERG, STEVEN · 2009 to 2020
$25.0M
Chronic Inflammation and CarcinogenesisZIABC011150 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DURUM, SCOTT · 2009 to 2025
$8.5M
Histopathology CoreZICEY000461 · NEI · NATIONAL EYE INSTITUTE · PI SCHNEEWEIS, DAVID · 2009 to 2022
$7.7M
Molecular And Immunopathology Of Experimental And Clinical Ocular DiseasesZIAEY000222 · NEI · NATIONAL EYE INSTITUTE · PI CHAN, CHI-CHAO · 2009 to 2015
$7.2M
Developing new immunotherapies based of CD4+ T cellsZIABC011037 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RESTIFO, NICHOLAS · 2009 to 2014
$4.4M
Functional Genomics of Inflammation and Critical IllnessZIACL001164 · CLC · CLINICAL CENTER · PI DANNER, ROBERT L · 2009 to 2018
$0k
Intramural NIH HHS Z99 CA999999Intramural NIH HHS ZIA BC010763Intramural NIH HHS ZIA BC011037NCI NIH HHS Y99 CA999999
6 · The paper itself

Abstract

Th17 cells have been described as short lived, but this view is at odds with their capacity to trigger protracted damage to normal and transformed tissues. We report that Th17 cells, despite displaying low expression of CD27 and other phenotypic markers of terminal differentiation, efficiently eradicated tumors and caused autoimmunity, were long lived, and maintained a core molecular signature resembling early memory CD8(+) cells with stem cell-like properties. In addition, we found that Th17 cells had high expression of Tcf7, a direct target of the Wnt and β-catenin signaling axis, and accumulated β-catenin, a feature observed in stem cells. In vivo, Th17 cells gave rise to Th1-like effector cell progeny and also self-renewed and persisted as IL-17A-secreting cells. Multipotency was required for Th17 cell-mediated tumor eradication because effector cells deficient in IFN-γ or IL-17A had impaired activity. Thus, Th17 cells are not always short lived and are a less-differentiated subset capable of superior persistence and functionality.

Indexed as

AnimalsCell DifferentiationCell SurvivalGene Expression ProfilingInterleukin-17MiceMice, TransgenicNeoplasmsStem CellsTh17 CellsTh1 CellsT-Lymphocyte SubsetsTumor Necrosis Factor Receptor Superfamily, Member 7Interleukin-17Tumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID22177921
PMCPMC3246082

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.