Skip to main navigation Skip to search Skip to main content

Endurance Exercise Attenuates Established Progressive Experimental Autoimmune Encephalomyelitis and Is Associated with an Amelioration of Innate Immune Responses in NOD Mice

Daniel Schiffmann, Victoria Lampkemeyer, Maren Lindner, Ann Katrin Fleck, Kathrin Koch, Melanie Eschborn, Marie Liebmann, Jan Kolja Strecker, Jens Minnerup, Heinz Wiendl, Luisa Klotz*

*Corresponding author for this work

Abstract

Multiple sclerosis (MS) is a chronic inflammatory autoimmune disease causing axonal degeneration and demyelination. Exercise in mice with active monophasic experimental autoimmune encephalomyelitis (EAE) attenuates disease severity associated with diverse impacts on T cell-mediated immunity. However, studies have so far focused on preventive approaches. In this study, we investigated the impact of endurance exercise on established EAE disease in a model of secondary progressive MS. When the exercise program on motorized running wheels was started at disease manifestation, the disease course was significantly ameliorated. This was associated with a significant decrease in B cell, dendritic cell, and neutrophil cell counts in the central nervous system (CNS). Furthermore, we observed an increased expression of major histocompatibility complex class II (MHC-II) as well as alterations in costimulatory molecule expression in CNS B cells and dendritic cells. In contrast, T cell responses were not altered in the CNS or periphery. Thus, exercise training is capable of attenuating the disease course even in established secondary progressive EAE, potentially via modulation of the innate immune compartment. Further studies are warranted to corroborate our findings and assess the potential of this lifestyle intervention as a complementary therapeutic strategy in secondary progressive MS patients.

Original languageEnglish
Article number15798
JournalInternational Journal of Molecular Sciences
Volume24
Issue number21
ISSN1661-6596
DOIs
Publication statusPublished - 11.2023

Funding

FundersFunder number
Deutsche ForschungsgemeinschaftSFB TR128, SFB1009, FOR 2879, HE111812, TRR 332

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Research Areas and Centers

    • Academic Focus: Center for Infection and Inflammation Research (ZIEL)

    DFG Research Classification Scheme

    • 2.23-07 Clinical Neurology, Neurosurgery and Neuroradiology
    • 2.21-05 Immunology

    Fingerprint

    Dive into the research topics of 'Endurance Exercise Attenuates Established Progressive Experimental Autoimmune Encephalomyelitis and Is Associated with an Amelioration of Innate Immune Responses in NOD Mice'. Together they form a unique fingerprint.

    Cite this