| Literature DB >> 28270598 |
Romain Marlin1, Angela Pappalardo1, Hannah Kaminski1,2, Carrie R Willcox3, Vincent Pitard1,4, Sonia Netzer1, Camille Khairallah1, Anne-Marie Lomenech5, Christelle Harly1,6, Marc Bonneville6, Jean-François Moreau1,7, Emmanuel Scotet6, Benjamin E Willcox3, Benjamin Faustin1, Julie Déchanet-Merville8,4.
Abstract
Human γδ T cells comprise a first line of defense through T-cell receptor (TCR) recognition of stressed cells. However, the molecular determinants and stress pathways involved in this recognition are largely unknown. Here we show that exposure of tumor cells to various stress situations led to tumor cell recognition by a Vγ8Vδ3 TCR. Using a strategy that we previously developed to identify antigenic ligands of γδ TCRs, annexin A2 was identified as the direct ligand of Vγ8Vδ3 TCR, and was found to be expressed on tumor cells upon the stress situations tested in a reactive oxygen species-dependent manner. Moreover, purified annexin A2 was able to stimulate the proliferation of a Vδ2neg γδ T-cell subset within peripheral blood mononuclear cells and other annexin A2-specific Vδ2neg γδ T-cell clones could be derived from peripheral blood mononuclear cells. We thus propose membrane exposure of annexin A2 as an oxidative stress signal for some Vδ2neg γδ T cells that could be involved in an adaptive stress surveillance.Entities:
Keywords: cell stress surveillance; cytomegalovirus; gamma-delta T cells; innate-like lymphocytes; tumor immunology
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Year: 2017 PMID: 28270598 PMCID: PMC5373368 DOI: 10.1073/pnas.1621052114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205