Fecal microbiota transplantation improves anti-PD-1 inhibitor efficacy in unresectable or metastatic solid cancers refractory to anti-PD-1 inhibitor

IF 20.6 1区 医学 Q1 MICROBIOLOGY
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引用次数: 0

Abstract

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.

Abstract Image

粪便微生物群移植可提高抗PD-1抑制剂难治性不可切除或转移性实体癌的疗效
肠道微生物群对免疫反应和免疫检查点抑制剂的疗效有重大影响。我们开展了一项临床试验(NCT04264975),将抗程序性死亡-1(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例抗PD-1难治性晚期实体瘤患者。在13名患者中,有6名患者通过粪便微生物群移植获得了持续的微生物群变化和临床获益,其中1名患者部分应答,5名患者病情稳定,客观应答率达到7.7%,疾病控制率达到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有关。我们从一名 FMT 反应者体内分离出了 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体内的肿瘤生长。此外,我们还发现唾液乳杆菌(Lactobacillus salivarius)和褶状乳杆菌(Bacteroides plebeius)可能会抑制抗肿瘤免疫。我们的研究结果表明,在晚期实体瘤,尤其是胃肠道癌症中,使用有益微生物群进行FMT治疗可以克服抗PD-1抑制剂的耐药性。
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来源期刊
Cell host & microbe
Cell host & microbe 生物-微生物学
CiteScore
45.10
自引率
1.70%
发文量
201
审稿时长
4-8 weeks
期刊介绍: Cell Host & Microbe is a scientific journal that was launched in March 2007. The journal aims to provide a platform for scientists to exchange ideas and concepts related to the study of microbes and their interaction with host organisms at a molecular, cellular, and immune level. It publishes novel findings on a wide range of microorganisms including bacteria, fungi, parasites, and viruses. The journal focuses on the interface between the microbe and its host, whether the host is a vertebrate, invertebrate, or plant, and whether the microbe is pathogenic, non-pathogenic, or commensal. The integrated study of microbes and their interactions with each other, their host, and the cellular environment they inhabit is a unifying theme of the journal. The published work in Cell Host & Microbe is expected to be of exceptional significance within its field and also of interest to researchers in other areas. In addition to primary research articles, the journal features expert analysis, commentary, and reviews on current topics of interest in the field.
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