Evidence map›Paper›PMID 24987392›Full record

ReviewFrontiers in immunology2014

Th17 cells in cancer: the ultimate identity crisis.

Stefanie R Bailey, Michelle H Nelson, Richard A Himes, Zihai Li, Shikhar Mehrotra, Chrystal M Paulos

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 187 papers.

0numbers the graph read from it
0cells of the map it votes in
187citing papers in PubMed
14.5field-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

187 citing papers in PubMed, 324 citations in OpenAlex.

  1. Trial
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  13. Microenvironment-based immunotherapy in oral cancer: a comprehensive review.Medical oncology (Northwood, London, England) · 2025
    Review
  14. Article
  15. Review
  16. Potential Pathogens Associated with Colorectal Cancer.Current pharmaceutical biotechnology · 2025
    Review
  17. Review
  18. Immunotherapy in Head and Neck Cancer.Cancer treatment and research · 2025
    Review
  19. Review
  20. Review

127 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

6 authors at 2 institutions in 1 country.

Stefanie R BaileyDepartment of Microbiology and Immunology, Medical University of South Carolina , Charleston, SC , USA ; Department of Surgery, Medical University of South Carolina , Charleston, SC , USA.
Michelle H NelsonDepartment of Microbiology and Immunology, Medical University of South Carolina , Charleston, SC , USA ; Department of Surgery, Medical University of South Carolina , Charleston, SC , USA.
Richard A HimesDepartment of Chemistry, College of Charleston , Charleston, SC , USA.
Zihai LiDepartment of Microbiology and Immunology, Medical University of South Carolina , Charleston, SC , USA.
Shikhar MehrotraDepartment of Surgery, Medical University of South Carolina , Charleston, SC , USA.
Chrystal M PaulosDepartment of Microbiology and Immunology, Medical University of South Carolina , Charleston, SC , USA ; Department of Surgery, Medical University of South Carolina , Charleston, SC , USA.
Medical University of South Carolina · USCollege of Charleston · US

Funding

TCR TRANSDUCED CDB T CELLS FOR ADOPTIVE IMMUNOTHERAPYP01CA154778 · NCI · LOYOLA UNIVERSITY CHICAGO · PI NISHIMURA, MICHAEL I. · 2011 to 2015
$15.4M
South Carolina Clinical & Translational Research Institute (SCTR)UL1TR000062 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T. · 2012 to 2014
$9.4M
Costimulatory mechanisms of antitumor Th17 cell immunityR01CA175061 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI PAULOS, CHRYSTAL MARY · 2013 to 2017
$1.5M
South Carolina Clinical & Translational Research Institute (SCTR)KL2TR000060 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T. · 2012 to 2014
$807k
NCATS NIH HHS KL2 TR000060NCATS NIH HHS UL1 TR000062NCI NIH HHS P01 CA154778NCI NIH HHS R01 CA175061
6 · The paper itself

Abstract

T helper 17 (Th17) cells play a complex and controversial role in tumor immunity and have been found to exhibit a fluctuating identity within the context of cancer. The recent, expanding literature on these cells attests to their puzzling nature, either promoting or suppressing tumor growth depending on the malignancy and course of therapeutic intervention investigated. This review addresses several newly appreciated factors that may help delineate Th17 cells' immunological properties in the context of cancer. Several reports suggest that inflammatory signals induced in the tumor milieu regulate the functional fate and antitumor activity of Th17 cells. Recent findings also point to significant alterations in Th17 cells due to their interplay with regulatory T lymphocytes and cytotoxic CD8(+) T cells within the tumor microenvironment. Finally, an appreciation for the stem cell-like properties of Th17 cells that augment their persistence and activity emerges from recent reports. The impact of these factors on Th17 cells' antitumor efficacy and how these factors may be exploited to improve cancer therapies will be discussed.

Indexed as

cancerIL-17AimmunotherapyplasticityRORγtTh17tumor microenvironment

Identifiers

PMID24987392
PMCPMC4060300
OpenAlexW2128792706

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.