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肠道微生物群和细胞治疗:影响和机制的意义。

The intestinal microbiota and cellular therapy: implications for impact and mechanisms.

机构信息

Division of Blood and Marrow Transplantation and Cellular Therapy, Department of Medicine, Stanford University School of Medicine, Stanford, CA.

出版信息

Blood. 2024 Oct 10;144(15):1557-1569. doi: 10.1182/blood.2024024219.

DOI:10.1182/blood.2024024219
PMID:39141827
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11830981/
Abstract

The microbiota, comprising bacteria, fungi, and viruses residing within our bodies, functions as a key modulator in host health and states, including immune responses. Studies have linked microbiota and microbiota-derived metabolites to immune cell functions. In this review, we probe the complex relationship between the human microbiota and clinical outcomes of cellular therapies that leverage immune cells to fight various cancers. With a particular emphasis on hematopoietic cell transplantation and chimeric antigen receptor T-cell therapy, we explore the potential mechanisms underpinning this interaction. We also highlight the interventional applications of the microbiota in cellular therapy while outlining future research directions in the field.

摘要

微生物组由存在于我们体内的细菌、真菌和病毒组成,是调节宿主健康和状态的关键因素,包括免疫反应。研究已经将微生物组和微生物衍生代谢物与免疫细胞功能联系起来。在这篇综述中,我们探讨了人类微生物组与利用免疫细胞对抗各种癌症的细胞疗法的临床结果之间的复杂关系。特别强调造血细胞移植和嵌合抗原受体 T 细胞疗法,我们探索了这种相互作用的潜在机制。我们还强调了微生物组在细胞治疗中的干预应用,同时概述了该领域的未来研究方向。

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Microbial metabolite enhances immunotherapy efficacy by modulating T cell stemness in pan-cancer.微生物代谢产物通过调节泛癌中的 T 细胞干性增强免疫疗法疗效。
Cell. 2024 Mar 28;187(7):1651-1665.e21. doi: 10.1016/j.cell.2024.02.022. Epub 2024 Mar 14.
2
Bile acids modified by the intestinal microbiota promote colorectal cancer growth by suppressing CD8 T cell effector functions.肠道微生物群修饰的胆汁酸通过抑制 CD8 T 细胞效应功能促进结直肠癌生长。
Immunity. 2024 Apr 9;57(4):876-889.e11. doi: 10.1016/j.immuni.2024.02.014. Epub 2024 Mar 12.
3
Third-party fecal microbiota transplantation for high-risk treatment-naïve acute GVHD of the lower GI tract.
第三方粪便微生物群移植治疗高危初治急性下胃肠道移植物抗宿主病。
Blood Adv. 2024 May 14;8(9):2074-2084. doi: 10.1182/bloodadvances.2024012556.
4
Urolithin A Hijacks ERK1/2-ULK1 Cascade to Improve CD8 T Cell Fitness for Antitumor Immunity.尿石素 A 劫持 ERK1/2-ULK1 级联反应以改善 CD8+T 细胞的抗肿瘤免疫功能。
Adv Sci (Weinh). 2024 May;11(18):e2310065. doi: 10.1002/advs.202310065. Epub 2024 Mar 6.
5
Altered microbial bile acid metabolism exacerbates T cell-driven inflammation during graft-versus-host disease.微生物胆汁酸代谢改变加剧移植物抗宿主病中的 T 细胞驱动的炎症。
Nat Microbiol. 2024 Mar;9(3):614-630. doi: 10.1038/s41564-024-01617-w. Epub 2024 Mar 1.
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Blood and guts: how the intestinal microbiome shapes hematopoiesis and treatment of hematologic disease.血与内脏:肠道微生物组如何塑造造血和血液病治疗。
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Inosine induces stemness features in CAR-T cells and enhances potency.肌苷诱导 CAR-T 细胞的干性特征并增强其效力。
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