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  3. Gut microbiota-derived TMAVA is a modulator of acute CNS-GVHD.
 

Gut microbiota-derived TMAVA is a modulator of acute CNS-GVHD.

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BORIS DOI
10.48620/89359
Date of Publication
September 1, 2025
Publication Type
Article
Division/Institute

Clinic of Visceral Su...

Department for BioMed...

Author
Chatterjee, Sangya
Rückert, Tamina
Martin, Ina
Michaeli, Elisa
Buescher, Joerg
Apostolova, Petya
Erny, Daniel
Lalioti, Maria-Eleni
Biavasco, Francesca
Hartmann, Alina
Runge, Solveig
Braun, Lukas M
Talvard-Balland, Nana
Adams, Rachael C
Schmitt-Graeff, Annette
Cook, James
Wenger, Valentin
Athanassopoulos, Dimitrios
Hasavci, Dilara
Vallejo-Janeta, Alexander Paolo
Blank, Thomas
Schaible, Philipp
Vinnakota, Janaki Manoja
Zähringer, Alexander
Ganal-Vonarburg, Stephanie C.
Clinic of Visceral Surgery and Medicine, Gastroenterology
Department for BioMedical Research, Forschungsgruppe Gastroenterologie / Mukosale Immunologie
Melchinger, Wolfgang
Pfeifer, Dietmar
Köhler, Natalie
Rosshart, Stephan P
Michonneau, David
Socié, Gérard
Andrieux, Geoffroy
Cabezas-Wallscheid, Nina
Boerries, Melanie
Prinz, Marco
Zeiser, Robert
Subject(s)

600 - Technology::610...

Series
Journal of Experimental Medicine
ISSN or ISBN (if monograph)
1540-9538
0022-1007
Publisher
Rockefeller University Press
Language
English
Publisher DOI
10.1084/jem.20242180
PubMed ID
40627379
Description
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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/213142
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jem_20242180.pdftextAdobe PDF9.87 MBpublished restricted
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