1. Synthetic retinoid-mediated preconditioning of cancer-associated fibroblasts and macrophages improves cancer response to immune checkpoint blockade.
- Author
-
Owaki T, Iida T, Miyai Y, Kato K, Hase T, Ishii M, Ando R, Hinohara K, Akashi T, Mizutani Y, Ishikawa T, Mii S, Shiraki Y, Esaki N, Yamamoto M, Tsukamoto T, Nomura S, Murakami T, Takahashi M, Yuguchi Y, Maeda M, Sano T, Sassa N, Matsukawa Y, Kawashima H, Akamatsu S, and Enomoto A
- Subjects
- Animals, Mice, Humans, Tetrahydronaphthalenes pharmacology, Retinoids pharmacology, Retinoids therapeutic use, Carcinoma, Renal Cell drug therapy, Carcinoma, Renal Cell immunology, Carcinoma, Renal Cell pathology, Tumor-Associated Macrophages drug effects, Tumor-Associated Macrophages immunology, Tumor-Associated Macrophages metabolism, Kidney Neoplasms drug therapy, Kidney Neoplasms immunology, Kidney Neoplasms pathology, Female, Cell Line, Tumor, Benzoates, Cancer-Associated Fibroblasts drug effects, Cancer-Associated Fibroblasts metabolism, Immune Checkpoint Inhibitors pharmacology, Immune Checkpoint Inhibitors therapeutic use, Tumor Microenvironment drug effects, Tumor Microenvironment immunology, Macrophages immunology, Macrophages drug effects, Macrophages metabolism
- Abstract
Background: The proliferation of cancer-associated fibroblasts (CAFs) hampers drug delivery and anti-tumor immunity, inducing tumor resistance to immune checkpoint blockade (ICB) therapy. However, it has remained a challenge to develop therapeutics that specifically target or modulate CAFs., Methods: We investigated the involvement of Meflin
+ cancer-restraining CAFs (rCAFs) in ICB efficacy in patients with clear cell renal cell carcinoma (ccRCC) and urothelial carcinoma (UC). We examined the effects of Am80 (a synthetic retinoid) administration on CAF phenotype, the tumor immune microenvironment, and ICB efficacy in cancer mouse models., Results: High infiltration of Meflin+ CAFs correlated with ICB efficacy in patients with ccRCC and UC. Meflin+ CAF induction by Am80 administration improved ICB efficacy in the mouse models of cancer. Am80 exerted this effect when administered prior to, but not concomitant with, ICB therapy in wild-type but not Meflin-deficient mice. Am80-mediated induction of Meflin+ CAFs was associated with increases in antibody delivery and M1-like tumor-associated macrophage (TAM) infiltration. Finally, we showed the role of Chemerin produced from CAFs after Am80 administration in the induction of M1-like TAMs., Conclusion: Our data suggested that Am80 administration prior to ICB therapy increases the number of Meflin+ rCAFs and ICB efficacy by inducing changes in TAM phenotype., (© 2024. The Author(s).)- Published
- 2024
- Full Text
- View/download PDF