| Literature DB >> 26405567 |
Mircea Chirica1, Lionel Le Bourhis2, Jacqueline Lehmann-Che3, Victor Chardiny2, Fatiha Bouhidel4, Laure Foulboeuf2, Jean Marc Gornet5, Nelson Lourenco5, Nicolas Dulphy2, Antoine Toubert2, Matthieu Allez6.
Abstract
Colorectal cancers (CRC) develop in the face of an important immune system associated with the intestinal mucosal tissue. The immune response against the tumor has been proposed to affect the prognosis of patients undergoing treatment for CRC. In this study T cells infiltrating the tumor were compared with T cells populating the unaffected neighboring mucosal tissue and cells from the peripheral blood. We observed that T cells from the tumor harbor an activated phenotype, with engagement of the NKG2D pathway in CD8 T cells. We show that mucosal and tumor-infiltrating T cells are enriched in NKG2D CD4 T cells, which exhibit cytotoxic functions. Finally, T cell populations in the tumor were modified according to its oncogenetic status, with higher percentages of CD8 T cells isolated from patients with microsatellite instable tumor status.Entities:
Keywords: Colon cancer; NKG2D; T cells; microsatellite instability
Year: 2015 PMID: 26405567 PMCID: PMC4570110 DOI: 10.1080/2162402X.2015.1016698
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110