Coexisting systemic and organ-specific autoimmunity in MOG-IgG1-associated disorders versus AQP4-IgG+ NMOSD.
AQP4-IgG neuromyelitis optica spectrum disorder
MOG-IgG-associated disorders
autoimmunity
humoral immunity
systemic lupus erythematous
Journal
Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185
Informations de publication
Date de publication:
04 2021
04 2021
Historique:
pubmed:
8
7
2020
medline:
25
9
2021
entrez:
8
7
2020
Statut:
ppublish
Résumé
Aquaporin-4 (AQP4) neuromyelitis optica spectrum disorder (NMOSD) has been demonstrated to be associated with non-organ and organ-specific autoantibodies (antinuclear antibody, extractable nuclear antibody, double-stranded DNA, muscle acetylcholine receptor antibody) and systemic autoimmune diseases. In this study, we evaluated whether a similar association with non-organ and organ-specifc autoantibodies occurs in patients with MOG-IgG1-associated disorders. We determined that MOG-IgG1 was not strongly associated with these organ and non-organ-specific autoantibodies. Systemic lupus erythematous (SLE) was significantly associated with AQP4-IgG+ NMOSD and not with MOGAD (
Identifiants
pubmed: 32633603
doi: 10.1177/1352458520933884
doi:
Substances chimiques
Aquaporin 4
0
Autoantibodies
0
Immunoglobulin G
0
Myelin-Oligodendrocyte Glycoprotein
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
630-635Subventions
Organisme : NCATS NIH HHS
ID : UL1 TR002377
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS113828
Pays : United States