Diversity of Tumor-Infiltrating, γδ T-Cell Abundance in Solid Cancers
Ghita Chabab,
Florence Boissière-Michot,
Caroline Mollevi,
Jeanne Ramos,
Evelyne Lopez-Crapez,
Pierre-Emmanuel Colombo,
William Jacot,
Nathalie Bonnefoy,
Virginie Lafont
Affiliations
Ghita Chabab
IRCM, Institut de Recherche en Cancérologie de Montpellier, INSERM U1194, Université de Montpellier, Institut régional du Cancer de Montpellier, 34298 Montpellier, France
Florence Boissière-Michot
Translational Research Department, Institut régional du Cancer de Montpellier, 34298 Montpellier, France
Caroline Mollevi
Institut régional du Cancer de Montpellier, 34298 Montpellier, France
Jeanne Ramos
Translational Research Department, Institut régional du Cancer de Montpellier, 34298 Montpellier, France
Evelyne Lopez-Crapez
IRCM, Institut de Recherche en Cancérologie de Montpellier, INSERM U1194, Université de Montpellier, Institut régional du Cancer de Montpellier, 34298 Montpellier, France
Pierre-Emmanuel Colombo
IRCM, Institut de Recherche en Cancérologie de Montpellier, INSERM U1194, Université de Montpellier, Institut régional du Cancer de Montpellier, 34298 Montpellier, France
William Jacot
IRCM, Institut de Recherche en Cancérologie de Montpellier, INSERM U1194, Université de Montpellier, Institut régional du Cancer de Montpellier, 34298 Montpellier, France
Nathalie Bonnefoy
IRCM, Institut de Recherche en Cancérologie de Montpellier, INSERM U1194, Université de Montpellier, Institut régional du Cancer de Montpellier, 34298 Montpellier, France
Virginie Lafont
IRCM, Institut de Recherche en Cancérologie de Montpellier, INSERM U1194, Université de Montpellier, Institut régional du Cancer de Montpellier, 34298 Montpellier, France
γδ T-cells contribute to the immune response against many tumor types through their direct cytolytic functions and their capacity to recruit and regulate the biological functions of other immune cells. As potent effectors of the anti-tumor immune response, they are considered an attractive therapeutic target for immunotherapies, but their presence and abundance in the tumor microenvironment are not routinely assessed in patients with cancer. Here, we validated an antibody for immunohistochemistry analysis that specifically detects all γδ T-cell subpopulations in healthy tissues and in the microenvironment of different cancer types. Tissue microarray analysis of breast, colon, ovarian, and pancreatic tumors showed that γδ T-cell density varies among cancer types. Moreover, the abundance of γδ tumor-infiltrating lymphocytes was variably associated with the outcome depending on the cancer type, suggesting that γδ T-cell recruitment is influenced by the context. These findings also suggest that γδ T-cell detection and analysis might represent a new and interesting diagnostic or prognostic marker.