Twenty-nine Vδ2+ γδ T cells subpopulations were automatically defined, according to the coexpression of 22 variables informative of Vδ2+ γδ T cells differentiation stages (CD45RA, CCR7, CD27, CD28, IL7R), cytotoxic potential (CD56, CD16), activation state (CD69, CD44, ICOS), replicative senescence (CD57), inhibitory signaling and tumor-promoting tolerance (PD-1, PD-L1, CTLA-4, BTLA, TIGIT), susceptibility to apoptosis (Fas), tumor cell recognition and costimulatory signaling (DNAM-1) (Appendix A). This evidence concerns the gene TIGIT and neoplasm.