肠道微生物源性TMAVA是急性CNS-GVHD的调节剂。

IF 12.6 1区 医学 Q1 IMMUNOLOGY
Journal of Experimental Medicine Pub Date : 2025-09-01 Epub Date: 2025-07-08 DOI:10.1084/jem.20242180
Sangya Chatterjee, Tamina Rückert, Ina Martin, Elisa Michaeli, Joerg Buescher, Petya Apostolova, Daniel Erny, Maria-Eleni Lalioti, Francesca Biavasco, Alina Hartmann, Solveig Runge, Lukas M Braun, Nana Talvard-Balland, Rachael C Adams, Annette Schmitt-Graeff, James Cook, Valentin Wenger, Dimitrios Athanassopoulos, Dilara Hasavci, Alexander Paolo Vallejo-Janeta, Thomas Blank, Philipp Schaible, Janaki Manoja Vinnakota, Alexander Zähringer, Stephanie C Ganal-Vonarburg, Wolfgang Melchinger, Dietmar Pfeifer, Natalie Köhler, Stephan P Rosshart, David Michonneau, Gérard Socié, Geoffroy Andrieux, Nina Cabezas-Wallscheid, Melanie Boerries, Marco Prinz, Robert Zeiser
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引用次数: 0

摘要

急性移植物抗宿主病(aGVHD)可通过小胶质细胞激活和T细胞浸润影响中枢神经系统(CNS),但肠道微生物群在CNS-aGVHD中的作用尚不清楚。在这里,我们使用抗生素处理的特异性无病原体(SPF)、无细菌(GF)和野生小鼠研究了微生物群在aGVHD期间小胶质细胞激活中的作用。抗生素介导的微生物群耗损导致脑内产生IFN-γ的T细胞浸润,通过TLR4/p38 MAPK途径激活小胶质细胞,以及SPF aGVHD小鼠的神经认知缺陷。小胶质细胞耗竭逆转了神经认知缺陷。GF和野生小鼠在异基因造血细胞移植(alloo - hct)后表现出相似的小胶质细胞激活。在机制上,抗生素治疗后小胶质细胞中细菌衍生代谢物N,N,N-三甲基-5-氨基戊酸(TMAVA)减少。ttmava抑制小胶质细胞中TLR4/p38 MAPK通路的活性,减轻肠道微生物群消耗介导的神经认知缺陷。此外,同种异体hct和GVHD发病后,患者血液中的ttmava丰度下降。总之,我们确定ttmava丢失是CNS-aGVHD的主要致病因素,为基于代谢物的治疗开辟了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut microbiota-derived TMAVA is a modulator of acute CNS-GVHD.

Acute graft-versus-host disease (aGVHD) can affect the central nervous system (CNS) through microglial activation and T cell infiltration, but the role of gut microbiota in CNS-aGVHD remains unclear. Here, we investigated the role of microbiota in microglial activation during aGVHD using antibiotic-treated specific pathogen-free (SPF), germ-free (GF), and wildling mice. Antibiotic-mediated microbiota depletion led to infiltration of IFN-γ-producing T cells in the brain, activation of microglia via the TLR4/p38 MAPK pathway, and neurocognitive deficits in SPF aGVHD mice. Microglial depletion reversed the neurocognitive deficits. GF and wildling mice treated with antibiotics exhibited similar microglial activation after allogeneic hematopoietic cell transplantation (allo-HCT). Mechanistically, the bacteria-derived metabolite N,N,N-trimethyl-5-aminovaleric acid (TMAVA) was decreased in microglia following antibiotic treatment. TMAVA administration suppressed TLR4/p38 MAPK pathway activity in microglia and alleviated gut microbiota depletion-mediated neurocognitive deficits. Additionally, TMAVA abundance decreased in patient blood after allo-HCT and after GVHD onset. In summary, we identify TMAVA loss as a central causative factor for CNS-aGVHD, opening new perspectives for a metabolite-based therapy.

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来源期刊
CiteScore
26.60
自引率
1.30%
发文量
189
审稿时长
3-8 weeks
期刊介绍: Since its establishment in 1896, the Journal of Experimental Medicine (JEM) has steadfastly pursued the publication of enduring and exceptional studies in medical biology. In an era where numerous publishing groups are introducing specialized journals, we recognize the importance of offering a distinguished platform for studies that seamlessly integrate various disciplines within the pathogenesis field. Our unique editorial system, driven by a commitment to exceptional author service, involves two collaborative groups of editors: professional editors with robust scientific backgrounds and full-time practicing scientists. Each paper undergoes evaluation by at least one editor from both groups before external review. Weekly editorial meetings facilitate comprehensive discussions on papers, incorporating external referee comments, and ensure swift decisions without unnecessary demands for extensive revisions. Encompassing human studies and diverse in vivo experimental models of human disease, our focus within medical biology spans genetics, inflammation, immunity, infectious disease, cancer, vascular biology, metabolic disorders, neuroscience, and stem cell biology. We eagerly welcome reports ranging from atomic-level analyses to clinical interventions that unveil new mechanistic insights.
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