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A Review of Compartmentalised Inflammation and Tertiary Lymphoid Structures in the Pathophysiology of Multiple Sclerosis

Rachael Kee, Michelle Naughton Orcid Logo, Gavin V. McDonnell, Owain Howell Orcid Logo, Denise C. Fitzgerald

Biomedicines, Volume: 10, Issue: 10, Start page: 2604

Swansea University Author: Owain Howell Orcid Logo

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Abstract

Multiple sclerosis (MS) is a chronic, immune-mediated, demyelinating disease of the central nervous system (CNS). The most common form of MS is a relapsing–remitting disease characterised by acute episodes of demyelination associated with the breakdown of the blood–brain barrier (BBB). In the relaps...

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Published in: Biomedicines
ISSN: 2227-9059
Published: MDPI AG 2022
Online Access: Check full text

URI: https://cronfa.swan.ac.uk/Record/cronfa65355
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Abstract: Multiple sclerosis (MS) is a chronic, immune-mediated, demyelinating disease of the central nervous system (CNS). The most common form of MS is a relapsing–remitting disease characterised by acute episodes of demyelination associated with the breakdown of the blood–brain barrier (BBB). In the relapsing–remitting phase there is often relative recovery (remission) from relapses characterised clinically by complete or partial resolution of neurological symptoms. In the later and progressive stages of the disease process, accrual of neurological disability occurs in a pathological process independent of acute episodes of demyelination and is accompanied by a trapped or compartmentalised inflammatory response, most notable in the connective tissue spaces of the vasculature and leptomeninges occurring behind an intact BBB. This review focuses on compartmentalised inflammation in MS and in particular, what we know about meningeal tertiary lymphoid structures (TLS; also called B cell follicles) which are organised clusters of immune cells, associated with more severe and progressive forms of MS. Meningeal inflammation and TLS could represent an important fluid or imaging marker of disease activity, whose therapeutic abrogation might be necessary to stop the most severe outcomes of disease.
Keywords: multiple sclerosis; progressive multiple sclerosis; nervous system; compartmentalised inflammation; meningeal inflammation; tertiary lymphoid structures; disease modifying therapy
College: Faculty of Medicine, Health and Life Sciences
Funders: This work was supported by HSC R&D Division, Public Health Agency [EAT/5496/18] (to R.K.) and Wellcome Trust Grant [110138/Z/15/Z] (to D.C.F.).
Issue: 10
Start Page: 2604