DietaryLactobacillus-Derived Exopolysaccharide Enhances Immune-Checkpoint Blockade Therapy

免疫系统 封锁 乳酸菌 生物 免疫检查点 癌症治疗 微生物学 免疫疗法 癌症研究 免疫学 细菌 癌症 化学 生物化学 受体 遗传学
作者
Hirotaka Kawanabe-Matsuda,Kazuyoshi Takeda,Marie Nakamura,Seiya Makino,Takahiro Karasaki,Kazuhiro Kakimi,Megumi Nishimukai,Tatsukuni Ohno,Jumpei Omi,Kuniyuki Kano,Akiharu Uwamizu,Hideo Yagita∥,Ivo G. Boneca,Gérard Eberl,Junken Aoki,Mark J. Smyth,Ko Okumura
出处
期刊:Cancer Discovery [American Association for Cancer Research]
卷期号:12 (5): 1336-1355 被引量:86
标识
DOI:10.1158/2159-8290.cd-21-0929
摘要

Microbes and their byproducts have been reported to regulate host health and immune functions. Here we demonstrated that microbial exopolysaccharide produced by Lactobacillus delbrueckii subsp. bulgaricus OLL1073R-1 (EPS-R1) induced CCR6+ CD8+ T cells of mice and humans. In mice, ingestion of EPS-R1 augmented antitumor effects of anti-CTLA-4 or anti-PD-1 monoclonal antibody against CCL20-expressing tumors, in which infiltrating CCR6+ CD8+ T cells were increased and produced IFNγ accompanied by a substantial immune response gene expression signature maintaining T-cell functions. Of note, the antitumor adjuvant effect of EPS-R1 was also observed in germ-free mice. Furthermore, the induction of CCR6 expression was mediated through the phosphorylated structure in EPS-R1 and a lysophosphatidic acid receptor on CD8+ T cells. Overall, we find that dietary EPS-R1 consumption induces CCR6+ CD8+ T cells in Peyer's patches, favoring a tumor microenvironment that augments the therapeutic effect of immune-checkpoint blockade depending on CCL20 production by tumors. Gut microbiota- and probiotic-derived metabolites are attractive agents to augment the efficacy of immunotherapies. Here we demonstrated that dietary consumption of Lactobacillus-derived exopolysaccharide induced CCR6+ CD8+ T cells in Peyer's patches and improved the tumor microenvironment to augment the therapeutic effects of immune-checkpoint blockade against CCL20-producing tumors. See related commentary by Di Luccia and Colonna, p. 1189. This article is highlighted in the In This Issue feature, p. 1171.
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