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Updated: Jun 22, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Abundant extracellular myelin in the meninges of patients with multiple sclerosis
E-J Kooi1, J van Horssen, M E Witte
1Department of Pathology, VU University Medical Centre, Amsterdam, the Netherlands. e.kooi@vumc.nl
Background:
In multiple sclerosis (MS) myelin debris has been observed within MS lesions, in cerebrospinal fluid and cervical lymph nodes, but the route of myelin transport out of the brain is unknown. Drainage of interstitial fluid from the brain parenchyma involves the perivascular spaces and leptomeninges, but the presence of myelin debris in these compartments has not been described.
Aims:
To determine whether myelin products are present in the meninges and perivascular spaces of MS patients.
Methods:
Formalin-fixed brain tissue containing meninges from 29 MS patients, 9 non-neurological controls, 6 Alzheimer's disease, 5 stroke, 5 meningitis and 7 leucodystrophy patients was investigated, and immunohistochemically stained for several myelin proteins [proteolipid protein (PLP), myelin basic protein (MBP), myelin oligodendrocyte glycoprotein (MOG) and 2',3'-cyclic nucleotide 3'-phosphodiesterase (CNPase)]. On brain material from MS patients and (non)neurological controls, PLP immunostaining was used to systematically investigate the presence of myelin debris in the meninges, using a semiquantitative scale.
Results:
Extensive extracellular presence of myelin particles, positive for PLP, MBP, MOG and CNPase in the leptomeninges of MS patients, was observed. Myelin particles were also observed in perivascular spaces of MS patients. Immunohistochemical double-labelling for macrophage and dendritic cell markers and PLP confirmed that the vast majority of myelin particles were located extracellularly. Extracellular myelin particles were virtually absent in meningeal tissue of non-neurological controls, Alzheimer's disease, stroke, meningitis and leucodystrophy cases.
Conclusions:
In MS leptomeninges and perivascular spaces, abundant extracellular myelin can be found, whereas this is not the case for controls and other neurological disease. This may be relevant for understanding sustained immunogenicity or, alternatively, tolerogenicity in MS.
Insights
Myelin debris, identified by myelin proteins like PLP, is abundant in the meninges and perivascular spaces of multiple sclerosis (MS) patients, but absent in controls. This finding offers insights into MS immunogenicity.
Area of Science:
- Neuroimmunology
- Neuropathology
Background:
- Myelin debris is observed in multiple sclerosis (MS) lesions, cerebrospinal fluid, and lymph nodes.
- The pathway for myelin transport out of the brain remains unknown.
- Myelin debris presence in the brain's perivascular spaces and leptomeninges has not been previously described.
Purpose of the Study:
- To investigate the presence of myelin products in the meninges and perivascular spaces of MS patients.
- To determine if myelin debris accumulates in these compartments during MS.
Main Methods:
- Immunohistochemical staining of formalin-fixed brain tissue from 29 MS patients and various control groups (non-neurological, Alzheimer's disease, stroke, meningitis, leucodystrophy).
- Specific staining for myelin proteins: proteolipid protein (PLP), myelin basic protein (MBP), myelin oligodendrocyte glycoprotein (MOG), and 2',3'-cyclic nucleotide 3'-phosphodiesterase (CNPase).
- Systematic investigation of PLP-positive myelin debris in the meninges using a semiquantitative scale.
Main Results:
- Extensive extracellular myelin particles, positive for PLP, MBP, MOG, and CNPase, were found in the leptomeninges of MS patients.
- Myelin particles were also detected in the perivascular spaces of MS patients.
- These extracellular myelin particles were nearly absent in all control groups, including non-neurological, Alzheimer's disease, stroke, meningitis, and leucodystrophy cases.
Conclusions:
- Abundant extracellular myelin is present in the leptomeninges and perivascular spaces of MS patients, but not in controls or other neurological diseases.
- This accumulation of myelin in specific compartments may play a role in the sustained immunogenicity or tolerogenicity observed in MS.
- Further research is needed to elucidate the precise mechanisms and implications of this finding in MS pathogenesis.
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