| Literature DB >> 32362028 |
Ghita Chabab1, Clément Barjon1,2, Naoill Abdellaoui1, Lucie Salvador-Prince1, Cécile Dejou1, Henri-Alexandre Michaud1, Florence Boissière-Michot3, Evelyne Lopez-Crapez1,3, William Jacot1,4, Didier Pourquier5, Nathalie Bonnefoy1, Virginie Lafont1.
Abstract
γδ 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 γδ T cells may also display pro-tumor activities. Here, we identified in blood from healthy donors a subpopulation of Vδ1T cells that represents around 20% of the whole Vδ1 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 αβ T cell proliferation). We then found that in human breast tumors, γδ T cells were present particularly in late stage breast cancer samples, and that ∼20% of tumor-infiltrating γδ T cells expressed CD73. Taken together, these results suggest that regulatory γδ 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. ©2020 Society for Leukocyte Biology.Entities:
Keywords: immunosuppression; non-conventional T cells; tumor microenvironment
Year: 2020 PMID: 32362028 DOI: 10.1002/JLB.3MA0420-278RR
Source DB: PubMed Journal: J Leukoc Biol ISSN: 0741-5400 Impact factor: 4.962