Evidence map›Paper›PMID 23034170›Full record

Trial reportJournal of immunology (Baltimore, Md. : 1950)2012

Tumor-infiltrating γδ T lymphocytes predict clinical outcome in human breast cancer.

Chunling Ma, Qunyuan Zhang, Jian Ye, Fang Wang, Yanping Zhang, Eric Wevers, Theresa Schwartz, Pamela Hunborg, Mark A Varvares, Daniel F Hoft and 2 more

Abstract readClinical Trial
In one paragraph

Trial report in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
119citing 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

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

  1. The prognostic values of FOXP3Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Pooled it
  2. Prognostic and predictive value of tumor-infiltrating lymphocytes in breast cancer: a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2016
    Pooled it
  3. Pooled it
  4. γδ T cells and cancer.The Journal of clinical investigation · 2026
    Review
  5. γδ T cells in colorectal and liver cancer.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. An organotypic human melanoma-in-skin model as anImmuno-oncology technology · 2024
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. γδ T cells: origin and fate, subsets, diseases and immunotherapy.Signal transduction and targeted therapy · 2023
    Review
  20. Article

59 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

12 authors.

Chunling MaDepartment of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO 63104, USA.
Qunyuan Zhang
Jian Ye
Fang Wang
Yanping Zhang
Eric Wevers
Theresa Schwartz
Pamela Hunborg
Mark A Varvares
Daniel F Hoft
Eddy C Hsueh
Guangyong Peng

Funding

T Regulatory Cells and Neonatal Innate ImmunityR21AI094478 · NIAID · SAINT LOUIS UNIVERSITY · PI KOENIG, JOYCE MARIE, PENG, GUANGYONG · 2012 to 2013
$413k
Commitment and Plasticity of Th17 cells and Tregs in the Tumor MicroenvironmentR21AI097852 · NIAID · SAINT LOUIS UNIVERSITY · PI PENG, GUANGYONG · 2012 to 2013
$413k
NIAID NIH HHS AI094478NIAID NIH HHS AI097852NIAID NIH HHS R21 AI094478NIAID NIH HHS R21 AI097852
6 · The paper itself

Abstract

Understanding and dissecting the role of different subsets of regulatory tumor-infiltrating lymphocytes (TILs) in the immunopathogenesis of individual cancer is a challenge for anti-tumor immunotherapy. High levels of γδ regulatory T cells have been discovered in breast TILs. However, the clinical relevance of these intratumoral γδ T cells is unknown. In this study, γδ T cell populations were analyzed by performing immunohistochemical staining in primary breast cancer tissues from patients with different stages of cancer progression. Retrospective multivariate analyses of the correlations between γδ T cell levels and other prognostic factors and clinical outcomes were completed. We found that γδ T cell infiltration and accumulation in breast tumor sites was a general feature in breast cancer patients. Intratumoral γδ T cell numbers were positively correlated with advanced tumor stages, HER2 expression status, and high lymph node metastasis but inversely correlated with relapse-free survival and overall survival of breast cancer patients. Multivariate and univariate analyses of tumor-infiltrating γδ T cells and other prognostic factors further suggested that intratumoral γδ T cells represented the most significant independent prognostic factor for assessing severity of breast cancer compared with the other known factors. Intratumoral γδ T cells were positively correlated with FOXP3(+) cells and CD4(+) T cells but negatively correlated with CD8(+) T cells in breast cancer tissues. These findings suggest that intratumoral γδ T cells may serve as a valuable and independent prognostic biomarker, as well as a potential therapeutic target for human breast cancer.

Indexed as

AdultAgedAged, 80 and overBiomarkersBreast NeoplasmsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell MovementDisease-Free SurvivalFemaleHumansImmunohistochemistryImmunotherapyMiddle AgedNeoplasm StagingReceptors, Antigen, T-Cell, gamma-deltaBiomarkersReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID23034170
PMCPMC4832413

What OpenQuestion holds

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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.