Author:
Douguet Laetitia,dit Hreich Serena Janho,Benzaquen Jonathan,Seguin Laetitia,Juhel Thierry,Dezitter Xavier,Duranton Christophe,Ryffel Bernhard,Kanellopoulos Jean,Delarasse Cecile,Renault Nicolas,Furman Christophe,Homerin Germain,Féral Chloé,Cherfils-Vicini Julien,Millet Régis,Adriouch Sahil,Ghinet Alina,Hofman Paul,Vouret-Craviari Valérie
Abstract
ABSTRACTOnly a subpopulation of non-small cell lung cancer (NSCLC) patients responds to immunotherapies, highlighting the urgent need to develop new therapeutic strategies to improve patient outcome. We developed a new chemical positive modulator (HEI3090) of the purinergic P2RX7 receptor that potentiates αPD-1 treatment to effectively control the growth of lung tumors in transplantable and oncogene-induced mouse models and triggers long lasting antitumor immune responses. Mechanistically, the molecule stimulates dendritic P2RX7 expressing cells to generate IL-18 which leads to the production of IFN-γ by Natural Killer and CD4+ T cells within tumors. Combined with immune checkpoint inhibitor, the molecule induces a complete tumor regression in 80% of LLC tumor bearing mice. Cured mice are also protected against tumor re-challenge due to a CD8-dependent protective response. Hence, combination treatment of small-molecule P2RX7 activator followed by immune checkpoint inhibitor represents a promising novel strategy that may be active against NSCLC.
Publisher
Cold Spring Harbor Laboratory