Commun Med (Lond). 2026 Apr 21. doi: 10.1038/s43856-026-01598-3. Online ahead of print.
ABSTRACT
BACKGROUND: Diffuse large B-cell lymphoma (DLBCL) is an aggressive malignancy where many patients relapse after standard therapy, necessitating novel approaches. Pyroptosis is an inflammatory cell death that can stimulate antitumor immunity. Histone deacetylases are frequently overexpressed in DLBCL and contribute to immune evasion. This study investigates whether combining the HDAC inhibitor chidamide with cisplatin and etoposide induces pyroptosis and enhances antitumor immune responses.
METHODS: We evaluated chidamide combined with cisplatin and etoposide in diffuse large B-cell lymphoma cell lines and syngeneic mouse models. Cell death mechanisms were analyzed using immunoblotting and imaging. Tumor growth and immune cell infiltration were assessed in immunocompetent mice, with the role of adaptive immunity evaluated through CD8-positive T cell depletion. Statistical analyses included analysis of variance where appropriate.
RESULTS: Here we show that chidamide synergistically potentiates cisplatin and etoposide efficacy by upregulating gasdermin E expression and promoting its caspase-3-dependent cleavage, thereby triggering pyroptosis. This combination remodels the tumor microenvironment, increasing infiltration of dendritic cells, natural killer cells, and CD8-positive T cells while reducing immunosuppressive macrophages. Depletion of CD8-positive T cells abolishes the therapeutic benefit, demonstrating their essential role.
CONCLUSIONS: The chidamide-cisplatin-etoposide combination triggers immunogenic pyroptosis via the caspase-3/gasdermin E axis and activates adaptive immunity. This regimen represents a promising therapeutic strategy for relapsed diffuse large B-cell lymphoma warranting clinical investigation.
PMID:42014876 | DOI:10.1038/s43856-026-01598-3
