封锁
免疫检查点
免疫系统
医学
代谢途径
免疫学
癌症研究
免疫疗法
内科学
新陈代谢
受体
作者
Iris L. Mimpen,Thomas Battaglia,Miguel Parra Martinez,Laurien Joanna Zeverijn,Birgit S. Geurts,Louisa Rose Hoes,Vincent van der Noort,Hans A. J. Gelderblom,Krijn Kristian Dijkstra,Lodewyk F.A. Wessels,Emile E. Voest
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2025-04-21
卷期号:85 (8_Supplement_1): 2212-2212
标识
DOI:10.1158/1538-7445.am2025-2212
摘要
Abstract Recent studies have identified a link between specific microbiome-derived bacteria and immune checkpoint blockade (ICB) efficacy. However, these species lack consistency across studies and their immunomodulatory mechanisms remain elusive. We hypothesized that community-level metabolic pathways across microbes are more suitable to predict ICB response. Using a curated resource of pan-cancer metagenomics data of ICB-treated patients, we identified several microbial metabolic processes significantly associated with response. Methylerythritol phosphate (MEP) pathway activity was associated with response and intratumoral Vδ2 T cell infiltration and induced Vδ2 T cell-mediated anti-tumor responses in patient-derived tumor organoids. In contrast, the riboflavin pathway was associated with ICB resistance, and its intermediates led to mucosal-associated invariant T (MAIT) cell-mediated immune suppression. Collectively, our results highlight the relevance and complexity of metabolite-mediated microbiome-immune crosstalk. Citation Format: Iris L. Mimpen, Thomas W. Battaglia, Miguel Parra Martinez, Laurien J. Zeverijn, Birgit S. Geurts, Louisa R. Hoes, Vincent van der Noort, Hans Gelderblom, Krijn K. Dijkstra, Lodewyk F. Wessels, Emile E. Voest. Microbial metabolic pathways guide response to immune checkpoint blockade therapy [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 2212.
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