Antibodies against Myelin Lipids in Multiple Sclerosis

2017 ◽  
Vol 43 (8) ◽  
pp. 875-880 ◽  
Author(s):  
M. V. Ivanova ◽  
M. N. Zakharova
2021 ◽  
pp. 577698
Author(s):  
Sara Ribes García ◽  
Bonaventura Casanova Estruch ◽  
Fernando Gómez Pajares ◽  
María Aranzazu Juan Blanco

2007 ◽  
Vol 14 (2) ◽  
pp. 183-187 ◽  
Author(s):  
LM Villar ◽  
N. García-Barragán ◽  
M. Espiño ◽  
E. Roldán ◽  
MC Sádaba ◽  
...  

Oligoclonal IgM bands (OCMB) against myelin lipids predict an aggressive multiple sclerosis (MS) course. However, the clinical significance of OCMB without lipid specificity, present in other MS patients, remains unknown. We describe here a characterization of these antibodies and study their role in MS progression. Fifty-four MS patients showing CSF-restricted OCMB were included in this study at disease onset and followed-up during 61.1 ± 2.7 months. The specificity of OCMB and the CSF B-cell profile were investigated. A second CSF IgM study was performed in a group of eight patients. Thirty-eight patients showed OCMB against myelin lipids (M+L+) and other sixteen had OCMB lacking this specificity (M+L-). The CD5+ B cell subpopulation, responsible for most persistent IgM responses, was considerably higher in M+L+ than in M+L- patients (3.3 ± 0.6% versus 0.8 ± 0.2, P = 0.009). In addition, M+L+ bands persisted during disease course, while M+L- disappeared during follow-up. M+L+ patients suffered more relapses (4.2 ± 0.6 versus 1.6 ± 0.3, P = 0.002) and reached higher disability (EDSS score of 2.2 ± 0.2 versus 1.2 ± 0.2, P = 0.02) than M+L- group. These data corroborate that anti-lipid OCMB associate with an aggressive MS course and show that OCMB that do not recognize myelin lipids represent a transient immune response related to a more benign disease course. Multiple Sclerosis 2008; 14: 183—187. http://msj.sagepub.com


2009 ◽  
Vol 15 (9) ◽  
pp. 1011-1029 ◽  
Author(s):  
M Podbielska ◽  
EL Hogan

Myelin lipids have long been thought to play intriguing roles in the pathogenesis of multiple sclerosis (MS). This review summarizes current understanding of the molecular basis of MS with emphasis on the: (i.) physico-chemical properties, organization and accessibility of the lipids and their distribution within the myelin multilayer; (ii.) characterization of myelin lipid structures, and structure–function relationships relevant to MS mechanisms, and; (iii.) immunogenic and other features of lipids in MS including molecular mimicry, lipid enzyme genetic knockouts, glycolipid-reactive NKT cells, and monoclonal antibody-induced remyelination. New findings associate anti-lipid antibodies with pathophysiological biomarkers and suggest clinical utility. The structure of CD1d-lipid complexed with the lipophilic invariant T cell receptor (iTCR) may be crucial to understanding MS pathogenesis, and design of lipid antigen-specific therapeutics. Novel immuno-modulatory tools for treatment of autoimmune diseases including MS in which there is both constraint of inflammation and stimulation of remyelination are now emerging.


2014 ◽  
Vol 8 (4) ◽  
pp. 231-237
Author(s):  
M. V. Ivanova ◽  
A. I. Tukhvatulin ◽  
A. Sh. Dzharullaeva ◽  
D. Yu. Logunov ◽  
M. N. Zakharova

1996 ◽  
Vol 22 (3) ◽  
pp. 207-215 ◽  
Author(s):  
H. Li ◽  
M. L. Cuzner ◽  
J. Newcombe
Keyword(s):  

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