生物
罗伊乳杆菌
代谢物
色氨酸
免疫系统
癌症研究
微生物学
免疫学
细菌
乳酸菌
氨基酸
遗传学
生物化学
作者
Mackenzie Bender,Alex McPherson,Catherine M. Phelps,Surya Prakash Pandey,Colin R. Laughlin,Jake H. Shapira,Luzmariel Medina Sanchez,Mohit Rana,Tanner Richie,Tahliyah S. Mims,Angela M. Gocher-Demske,Luisa Cervantes‐Barragán,Steven J. Mullett,Stacy L. Gelhaus,Tullia C. Bruno,Nikki Cannon,John A. McCulloch,Dario A.A. Vignali,Reinhard Hinterleitner,Alok V. Joglekar
出处
期刊:Cell
[Cell Press]
日期:2023-04-01
卷期号:186 (9): 1846-1862.e26
被引量:418
标识
DOI:10.1016/j.cell.2023.03.011
摘要
Summary
The use of probiotics by cancer patients is increasing, including among those undergoing immune checkpoint inhibitor (ICI) treatment. Here, we elucidate a critical microbial-host crosstalk between probiotic-released aryl hydrocarbon receptor (AhR) agonist indole-3-aldehyde (I3A) and CD8 T cells within the tumor microenvironment that potently enhances antitumor immunity and facilitates ICI in preclinical melanoma. Our study reveals that probiotic Lactobacillus reuteri (Lr) translocates to, colonizes, and persists within melanoma, where via its released dietary tryptophan catabolite I3A, it locally promotes interferon-γ-producing CD8 T cells, thereby bolstering ICI. Moreover, Lr-secreted I3A was both necessary and sufficient to drive antitumor immunity, and loss of AhR signaling within CD8 T cells abrogated Lr's antitumor effects. Further, a tryptophan-enriched diet potentiated both Lr- and ICI-induced antitumor immunity, dependent on CD8 T cell AhR signaling. Finally, we provide evidence for a potential role of I3A in promoting ICI efficacy and survival in advanced melanoma patients.
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