Enhancing KDM5A and TLR activity improves the response to immune checkpoint blockade.

Journal Article (Journal Article)

Immune checkpoint blockade (ICB) therapies are now established as first-line treatments for multiple cancers, but many patients do not derive long-term benefit from ICB. Here, we report that increased amounts of histone 3 lysine 4 demethylase KDM5A in tumors markedly improved response to the treatment with the programmed cell death protein 1 (PD-1) antibody in mouse cancer models. In a screen for molecules that increased KDM5A abundance, we identified one (D18) that increased the efficacy of various ICB agents in three murine cancer models when used as a combination therapy. D18 potentiated ICB efficacy through two orthogonal mechanisms: (i) increasing KDM5A abundance, which suppressed expression of the gene PTEN (encoding phosphatase and tensin homolog) and increased programmed cell death ligand 1 abundance through a pathway involving PI3K-AKT-S6K1, and (ii) activating Toll-like receptors 7 and 8 (TLR7/8) signaling pathways. Combination treatment increased T cell activation and expansion, CD103+ tumor-infiltrating dendritic cells, and tumor-associated M1 macrophages, ultimately enhancing the overall recruitment of activated CD8+ T cells to tumors. In patients with melanoma, a high KDM5A gene signature correlated with KDM5A expression and could potentially serve as a marker of response to anti-PD-1 immunotherapy. Furthermore, our results indicated that bifunctional agents that enhance both KDM5A and TLR activity warrant investigation as combination therapies with ICB agents.

Full Text

Duke Authors

Cited Authors

  • Wang, L; Gao, Y; Zhang, G; Li, D; Wang, Z; Zhang, J; Hermida, LC; He, L; Wang, Z; Si, J; Geng, S; Ai, R; Ning, F; Cheng, C; Deng, H; Dimitrov, DS; Sun, Y; Huang, Y; Wang, D; Hu, X; Wei, Z; Wang, W; Liao, X

Published Date

  • September 9, 2020

Published In

Volume / Issue

  • 12 / 560

PubMed ID

  • 32908002

Pubmed Central ID

  • 32908002

Electronic International Standard Serial Number (EISSN)

  • 1946-6242

Digital Object Identifier (DOI)

  • 10.1126/scitranslmed.aax2282

Language

  • eng

Conference Location

  • United States