Lozano Garcia, EsterMena, Mari-PauDíaz Sánchez, TaniaRosiñol Dachs, Laura2025-05-202025-05-202025-042051-1426https://hdl.handle.net/2445/221140Presence of plate-bound PVR or nectin-2 at 2 µg/mL did not significantly modify cell viability nor frequency of proliferating cells compared to isotype control. As expected, Treg conditions significantly increased FoxP3 expression (paired T test p<0.0001, n=6) which was accompanied by elevation of CD226 levels (p=0.0026). Surprisingly, Treg conditions led to reduction of TIGIT expression (p=0.0039) and CD96 (p=0.084). In addition, PVR ligation resulted in a higher frequency of IL10-producing cells in Th0 conditions (p=0.0193), most of them expressing high levels of CD226 (78.48% ± 2.324), CD96 (59.87% ± 4.032), and to a lesser extent, TIGIT (39.82% ± 4.043). Consistently, under these experimental conditions dual blockade of TIGIT and CD96 did not abrogate the increase in the percentage of IL-10 producing cells, suggesting that PVR binds CD226 expressing cells to upregulate IL-10 production.1 p.application/pdfengcc-by-nc (c) Lozano Garcia, Ester et al., 2025http://creativecommons.org/licenses/by-nc/4.0/Cèl·lules TMieloma múltipleT cellsMultiple myelomaPVR–CD226 interaction regulates IL-10 production during human T cell differentiationinfo:eu-repo/semantics/article7580162025-05-20info:eu-repo/semantics/openAccess