Nature immunology · 2026
Compartment-specific PPARδ activity controls the outcome of cancer-immune cell competition and immunotherapy efficacy.
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Bunk Paul, Ergin Ilgin, Maher Timothy, Shah Vyom, Bonney Julia R, Kumar Lokesh B S S, Chung Charlie, Wellhausen Nils, Moresco Philip, Shao Sarah, Habel Jill, Mandati Vinay, Rubino Rachel, Rivadeneira David E, Wilkinson John E, Herrero Laura, Westcott Peter M K, Weinberg Samuel E, Gill Saar I, Agar Nathalie Y R, Beyaz Semir
Аннотация
Most patients with solid tumors fail to sustain antitumor immunity, in part because immune cells cannot outcompete cancer cells inside the immunosuppressive tumor microenvironment. Here, we show the lipid-sensing transcription factor PPARδ is a compartment-specific determinant of cancer-immune fitness balance and immunotherapy efficacy. Activating PPARδ in cancer cells promotes their growth and impairs antitumor immunity, whereas activating it in immune cells drives tumor suppression and overrides tumor-promoting effects of cancer-intrinsic activation. Mechanistically, PPARδ enhances CD8+ T cell fitness against cancer through effector-associated chromatin remodeling and Cpt1a-mediated fatty acid oxidation. Therapeutically, PPARδ-activated CD8+ T cells sensitize immunotherapy-resistant microsatellite stable metastatic colorectal cancer to checkpoint blockade in mice, and pharmacological or genetic PPARδ activation enhances human chimeric antigen receptor T cell function. These findings identify compartment-specific PPARδ activity as a targetable driver of immune cell fitness that can be harnessed to improve outcomes in immunotherapy-resistant tumors.