免疫系统
肠道菌群
CD8型
T细胞
抗原
免疫学
丁酸盐
抗原呈递
癌症研究
生物
微生物学
细胞毒性T细胞
医学
发酵
体外
生物化学
食品科学
作者
Mireia Uribe‐Herranz,Stavros Rafail,Silvia Beghi,Luis Gil‐de‐Gómez,Ioannis I. Verginadis,Kyle Bittinger,Sergei Pustylnikov,Stefano Pierini,Renzo Perales‐Linares,Ian A. Blair,Clementina Mesaros,Nathaniel W. Snyder,Frederic D. Bushman,Constantinos Koumenis,Andrea Facciabene
摘要
Alterations in gut microbiota impact the pathophysiology of several diseases, including cancer. Radiotherapy (RT), an established curative and palliative cancer treatment, exerts potent immune modulatory effects, inducing tumor-associated antigen (TAA) cross-priming with antitumor CD8+ T cell elicitation and abscopal effects. We tested whether the gut microbiota modulates antitumor immune response following RT distal to the gut. Vancomycin, an antibiotic that acts mainly on gram-positive bacteria and is restricted to the gut, potentiated the RT-induced antitumor immune response and tumor growth inhibition. This synergy was dependent on TAA cross presentation to cytolytic CD8+ T cells and on IFN-γ. Notably, butyrate, a metabolite produced by the vancomycin-depleted gut bacteria, abrogated the vancomycin effect. In conclusion, depletion of vancomycin-sensitive bacteria enhances the antitumor activity of RT, which has important clinical ramifications.
科研通智能强力驱动
Strongly Powered by AbleSci AI