DPP9-mediated inflammasome repression protects against checkpoint inhibitor lung toxicity
Brewer, J. R.; Han, A.; Nassar, A. H.; Farhat, E. B.; Blackburn, H. N.; Xiao, T.; Mirza, H.; Mowel, W. K.; Sefik, E.; Hartner, S.; Chiorazzi, M.; Itoh, T.; Oh, M.-H.; Madden, M. Z.; Rangavajhula, A.; Adib, E.; Saleh, M. J.; Machaalani, M.; Rakaee, M.; Tafavvoghi, M.; Quattropani, C.; Gazetos, N.; Gerber, D.; Fattah, F.; SoRelle, J. A.; Choo, D.; von Itzstein, M. S.; Bevans-Fonti, S.; Ghanbar, M.; Suresh, K.; Mazumder, T.; Ye, C. J.; Choueiri, T. K.; Gusev, A.; Flavell, R. A.
Show abstract
Over one million patients receive cancer immunotherapy annually, yet the mechanisms underlying life-threatening immune-mediated toxicities remain poorly understood. Checkpoint inhibitor pneumonitis (CIP) is the leading cause of immunotherapy-related mortality, with a case fatality rate approaching 10%, and no genetic risk factors have been described to date. We identified Dipeptidyl-peptidase 9 (DPP9) as the first genetic susceptibility gene for CIP in a clinico-genomics cohort of 4,397 patients treated with immune checkpoint inhibitors. Mechanistically, DPP9 suppresses CARD8 inflammasome activation and IL-18 secretion in human monocytes, a pathway which is engaged prior to CIP onset, with IL-18 selectively elevated in the plasma of patients who subsequently develop CIP. Myeloid-restricted ablation of Dpp8 and Dpp9 in mice recapitulated the pulmonary histopathological and immunological hallmarks of CIP, including granuloma formation, accumulation of IFN{gamma}-producing T cells and monocyte-derived macrophages. Each of these phenotypes were driven by excessive IL-18 secretion. Together, these findings establish DPP9 as a genetic determinant of CIP and nominate IL-18 blockade as a mechanistically rational therapeutic strategy.
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