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IL-10-dependent Tr1 cells attenuate astrocyte activation and ameliorate chronic central nervous system inflammation.

Authors :
Mayo L
Cunha AP
Madi A
Beynon V
Yang Z
Alvarez JI
Prat A
Sobel RA
Kobzik L
Lassmann H
Quintana FJ
Weiner HL
Source :
Brain : a journal of neurology [Brain] 2016 Jul; Vol. 139 (Pt 7), pp. 1939-57. Date of Electronic Publication: 2016 May 31.
Publication Year :
2016

Abstract

SEE WINGER AND ZAMVIL DOI101093/BRAIN/AWW121 FOR A SCIENTIFIC COMMENTARY ON THIS ARTICLE: The innate immune system plays a central role in the chronic central nervous system inflammation that drives neurological disability in progressive forms of multiple sclerosis, for which there are no effective treatments. The mucosal immune system is a unique tolerogenic organ that provides a physiological approach for the induction of regulatory T cells. Here we report that nasal administration of CD3-specific antibody ameliorates disease in a progressive animal model of multiple sclerosis. This effect is IL-10-dependent and is mediated by the induction of regulatory T cells that share a similar transcriptional profile to Tr1 regulatory cells and that suppress the astrocyte inflammatory transcriptional program. Treatment results in an attenuated inflammatory milieu in the central nervous system, decreased microglia activation, reduced recruitment of peripheral monocytes, stabilization of the blood-brain barrier and less neurodegeneration. These findings suggest a new therapeutic approach for the treatment of progressive forms of multiple sclerosis and potentially other types of chronic central nervous system inflammation.<br /> (© The Author (2016). Published by Oxford University Press on behalf of the Guarantors of Brain.)

Details

Language :
English
ISSN :
1460-2156
Volume :
139
Issue :
Pt 7
Database :
MEDLINE
Journal :
Brain : a journal of neurology
Publication Type :
Academic Journal
Accession number :
27246324
Full Text :
https://doi.org/10.1093/brain/aww113