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.
| Originalsprache | Englisch |
|---|---|
| Aufsatznummer | 15798 |
| Zeitschrift | International Journal of Molecular Sciences |
| Jahrgang | 24 |
| Ausgabenummer | 21 |
| ISSN | 1661-6596 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 11.2023 |
Fördermittel
This research was funded by the “Deutsche Forschungsgemeinschaft” (DFG) SFB TR128 (project A08 to L.K.) and SFB1009 (project A03 to L.K.), (DFG) TRR 332 (project B02 to L.K.), (DFG) FOR 2879 (project C1 to L.K. and H.W.), as well as by the Innovative Medical Research program (IMF, Medical Faculty, University of Münster) grant number HE111812 to L.K.
| Träger | Trägernummer |
|---|---|
| Deutsche Forschungsgemeinschaft | SFB TR128, SFB1009, FOR 2879, HE111812, TRR 332 |
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
Strategische Forschungsbereiche und Zentren
- Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)
DFG-Fachsystematik
- 2.23-07 Klinische Neurologie, Neurochirurgie und Neuroradiologie
- 2.21-05 Immunologie
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