Hepatology (Baltimore, Md.) · 2025
Tumor site influences efficacy of MEKi and immunotherapy combinations in a preclinical model of cholangiocarcinoma.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Hammons Jacklyn N, Warren Emilie K, Wittling Megen C, Bennett Frances J, Rangel-Rivera Guillermo O, Mack Alexis F, Phillips Maggie J, Robinson Brian S, Krasinskas Alyssa M, Horvat Natalie K, Ruffin Ayana T, Liu Yuan, Cao Yichun, Azad Nilofer N S, Yarchoan Mark M, Heumann Thatcher, Keler Tibor, Maithel Shishir K, Paulos Chrystal M, Lesinski Gregory B
Аннотация
BACKGROUND AND AIMS: Although chemotherapy and anti-PD-L1 antibodies are the standard of care for cholangiocarcinoma (CCA), resistance is common and limits durable benefits for patients. This hurdle underscores the urgent need to innovate combination approaches that promote durable immunity in patients. MEK inhibitors (MEKi) have shown potential to enhance immunotherapy in CCA models, but early clinical trials combining MEKi with anti-PD-L1 therapy have yielded suboptimal results.
APPROACH AND RESULTS: We hypothesized that the addition of a CD27 agonist would salvage MEKi-induced T cell impairment and reduce CCA burden in vivo. We show that CD27 agonism potentiates T cell activation in the presence of MEKi in vitro. Further, triple therapy with CD27 agonist, anti-PD-L1, and MEKi elicits efficacy in a subcutaneous CCA model, accompanied by increases in tumor-infiltrating CD8 + T cells with memory phenotypes. Although triple therapy enhanced CD8 + T cell infiltration in mice with orthotopic CCA liver tumors, its impact on overall survival was less pronounced. Further investigation revealed that orthotopic CCA tumors harbored more CD11b + Gr-1 + cells when compared to either subcutaneous CCA tumors or to normal liver. Finally, in mice with orthotopic CCA tumors treated with triple therapy, depletion of Gr-1 + cells triggered severe toxicity, characterized by rapid weight loss and uncontrolled systemic and hepatic inflammation.
CONCLUSIONS: These findings identify myeloid cells as key mediators of both immunotherapy resistance and toxicity in CCA, highlighting the critical importance of tumor site and use of physiologically relevant preclinical models when evaluating immunotherapy strategies.
APPROACH AND RESULTS: We hypothesized that the addition of a CD27 agonist would salvage MEKi-induced T cell impairment and reduce CCA burden in vivo. We show that CD27 agonism potentiates T cell activation in the presence of MEKi in vitro. Further, triple therapy with CD27 agonist, anti-PD-L1, and MEKi elicits efficacy in a subcutaneous CCA model, accompanied by increases in tumor-infiltrating CD8 + T cells with memory phenotypes. Although triple therapy enhanced CD8 + T cell infiltration in mice with orthotopic CCA liver tumors, its impact on overall survival was less pronounced. Further investigation revealed that orthotopic CCA tumors harbored more CD11b + Gr-1 + cells when compared to either subcutaneous CCA tumors or to normal liver. Finally, in mice with orthotopic CCA tumors treated with triple therapy, depletion of Gr-1 + cells triggered severe toxicity, characterized by rapid weight loss and uncontrolled systemic and hepatic inflammation.
CONCLUSIONS: These findings identify myeloid cells as key mediators of both immunotherapy resistance and toxicity in CCA, highlighting the critical importance of tumor site and use of physiologically relevant preclinical models when evaluating immunotherapy strategies.