Differential contribution of immune effector mechanisms to cortical demyelination in multiple sclerosis

Abstract: Cortical demyelination is a widely recognized hallmark of multiple sclerosis (MS) and correlate of disease progression and cognitive decline. The pathomechanisms initiating and driving gray matter damage are only incompletely understood. Here, we determined the infiltrating leukocyte subpopulations in 26 cortical demyelinated lesions of biopsied MS patients and assessed their contribution to cortical lesion formation in a newly developed mouse model. We find that conformation-specific anti-myelin antibodies contribute to cortical demyelination even in the absence of the classical complement pathway. T cells and natural killer cells are relevant for intracortical type 2 but dispensable for subpial type 3 lesions, whereas CCR2+ monocytes are required for both. Depleting CCR2+ monocytes in marmoset monkeys with experimental autoimmune encephalomyelitis using a novel humanized CCR2 targeting antibody translates into significantly less cortical demyelination and disease severity. We conclude that biologics depleting CCR2+ monocytes might be attractive candidates for preventing cortical lesion formation and ameliorating disease progression in MS

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch
Notes
Acta neuropathologica. - 134 (2017) , 15-34, ISSN: 0001-6322

Event
Veröffentlichung
(where)
Freiburg
(who)
Universität
(when)
2019
Creator
Lagumersindez Denis, Nielsen
Wrzos, Claudia
Mack, Matthias
Winkler, Anne
van der Meer, Franziska
Reinert, Marie C.
Hollasch, Heiko
Flach, Anne
Brühl, Hilke
Cullen, Eilish
Schlumbohm, Christina
Fuchs, Eberhard
Linington, Christopher
Barrantes-Freer, Alonso
Metz, Imke
Wegner, Christiane
Liebetanz, David
Prinz, Marco
Brück, Wolfgang
Stadelmann, Christine
Nessler, Stefan Alexander
Contributor

DOI
10.1007/s00401-017-1706-x
URN
urn:nbn:de:bsz:25-freidok-1424445
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
25.03.2025, 1:54 PM CET

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Associated

Time of origin

  • 2019

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