4.5 Article

Identification of a regulatory Vδ1 gamma delta T cell subpopulation expressing CD73 in human breast cancer

Journal

JOURNAL OF LEUKOCYTE BIOLOGY
Volume 107, Issue 6, Pages 1057-1067

Publisher

OXFORD UNIV PRESS
DOI: 10.1002/JLB.3MA0420-278RR

Keywords

immunosuppression; non-conventional T cells; tumor microenvironment

Funding

  1. Institute National de la Sante et de la RechercheMedicale (INSERM)
  2. Universite deMontpellier
  3. Institut Regional du Cancer de Montpellier (ICM)
  4. SIRIC Montpellier Cancer [INCa_Inserm_DGOS_12553]
  5. Ligue contre le Cancer
  6. Fondation pour la Recherche Medicale
  7. Clinical Resources Center of the Montpellier Cancer Institute (CRB-ICM) [BB-033-00059]
  8. French National Research Agency [ANR-10-INBS-04]

Ask authors/readers for more resources

gamma delta T cells contribute to the immune response against many cancers, notably through their powerful effector functions that lead to the elimination of tumor cells and the recruitment of other immune cells. However, their presence in the tumor microenvironment has been associated with poor prognosis in breast, colon, and pancreatic cancer, suggesting that gamma delta T cells may also display pro-tumor activities. Here, we identified in blood from healthy donors a subpopulation of V delta 1T cells that represents around 20% of the whole V delta 1 population, expresses CD73, and displays immunosuppressive phenotype and functions (i.e., production of immunosuppressive molecules, such as IL-10, adenosine, and the chemotactic factor IL-8, and inhibition of alpha beta T cell proliferation). We then found that in human breast tumors, gamma delta T cells were present particularly in late stage breast cancer samples, and that similar to 20% of tumor-infiltrating gamma delta T cells expressed CD73. Taken together, these results suggest that regulatory gamma delta T cells are present in the breast cancer microenvironment and may display immunosuppressive functions through the production of immunosuppressive molecules, such as IL-10, IL-8, and adenosine, thus promoting tumor growth.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available