Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea.
Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea; Genome and Company, Suwon-si 16229, Gyeonggi-do, Republic of Korea.
Cell Host Microbe. 2024 Aug 14;32(8):1380-1393.e9. doi: 10.1016/j.chom.2024.06.010. Epub 2024 Jul 25.
The gut microbiome significantly influences immune responses and the efficacy of immune checkpoint inhibitors. We conducted a clinical trial (NCT04264975) combining an anti-programmed death-1 (PD-1) inhibitor with fecal microbiota transplantation (FMT) from anti-PD-1 responder in 13 patients with anti-PD-1-refractory advanced solid cancers. FMT induced sustained microbiota changes and clinical benefits in 6 of 13 patients, with 1 partial response and 5 stable diseases, achieving an objective response rate of 7.7% and a disease control rate of 46.2%. The clinical response correlates with increased cytotoxic T cells and immune cytokines in blood and tumors. We isolated Prevotella merdae Immunoactis from a responder to FMT, which stimulates T cell activity and suppresses tumor growth in mice by enhancing cytotoxic T cell infiltration. Additionally, we found Lactobacillus salivarius and Bacteroides plebeius may inhibit anti-tumor immunity. Our findings suggest that FMT with beneficial microbiota can overcome resistance to anti-PD-1 inhibitors in advanced solid cancers, especially gastrointestinal cancers.
肠道微生物群对免疫反应和免疫检查点抑制剂的疗效有显著影响。我们进行了一项临床试验(NCT04264975),将抗 PD-1 抑制剂与来自抗 PD-1 应答者的粪便微生物群移植(FMT)相结合,治疗 13 名抗 PD-1 难治性晚期实体瘤患者。FMT 在 13 名患者中的 6 名中诱导了持续的微生物群变化和临床获益,其中 1 名部分缓解,5 名疾病稳定,客观缓解率为 7.7%,疾病控制率为 46.2%。临床反应与血液和肿瘤中细胞毒性 T 细胞和免疫细胞因子的增加相关。我们从 FMT 的应答者中分离出 Prevotella merdae Immunoactis,它通过增强细胞毒性 T 细胞浸润来刺激 T 细胞活性并抑制小鼠肿瘤生长。此外,我们发现乳杆菌唾液和拟杆菌 plebeius 可能抑制抗肿瘤免疫。我们的研究结果表明,用有益的微生物群进行 FMT 可以克服晚期实体瘤,特别是胃肠道癌症对抗 PD-1 抑制剂的耐药性。