The Immunomodulatory Potential of Short-Chain Fatty Acids in Multiple Sclerosis

Author:

Barcutean Laura1ORCID,Maier Smaranda1ORCID,Burai-Patrascu Mihai2ORCID,Farczadi Lenard3,Balasa Rodica1

Affiliation:

1. Neurology Department, University of Medicine, Pharmacy, Science and Technology “George Emil Palade” Targu Mures, 540142 Targu Mures, Mures, Romania

2. Molecular Forecaster Inc., Montreal, QC H3A 2L1, Canada

3. Center for Advanced Medical and Pharmaceutical Research, University of Medicine, Pharmacy, Science, and Technology “George Emil Palade” Targu Mures, 540142 Targu Mures, Mures, Romania

Abstract

Multiple sclerosis (MS) is a chronic inflammatory and neurodegenerative central nervous system (CNS) disorder, characterized by focal inflammation, demyelination, irreversible axonal loss and neurodegeneration. The proposed mechanism involves auto-reactive T lymphocytes crossing the blood–brain barrier (BBB), contributing to inflammation and demyelination. Pro-inflammatory Th1 and Th17 lymphocytes are pivotal in MS pathogenesis, highlighting an imbalanced interaction with regulatory T cells. Dysbiosis in the gut microbiota, characterized by microbial imbalance is implicated in systemic inflammation, yet its exact role in MS remains elusive. Short-chain fatty acids (SCFAs), including valerate, butyrate, propionate, and acetate, produced through dietary fiber fermentation by the gut microbiota, modulate inflammation and immune responses. Particularly, butyrate and propionate exhibit pronounced anti-inflammatory effects in both the gut and CNS. These SCFAs influence regulatory T lymphocyte expression and BBB permeability. This review discusses the potential therapeutic implications of SCFA in MS, highlighting their ability to modulate the gut–brain axis and restore immune balance.

Funder

Ministry of Research, Innovation and Digitalization, CNCS–UEFISCDI

Publisher

MDPI AG

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