| Literature DB >> 33659007 |
Keita Takahashi1, Hideyuki Takeuchi1, Ryoko Fukai1, Haruko Nakamura1, Keisuke Morihara1, Yuichi Higashiyama1, Toshiyuki Takahashi2, Hiroshi Doi1, Fumiaki Tanaka1.
Abstract
Here we report three cases of anti-myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) mimicking multiple sclerosis in which seropositivity for anti-MOG antibodies occurred during disease-modifying drug dimethyl fumarate (DMF) treatment. These patients developed relapses with anti-MOG antibody seroconversion after switching from fingolimod or steroid pulse therapy to DMF, which was associated with peripheral lymphocyte recovery. MOGAD is considered a humoral immune disease, and DMF reportedly enhances Th2-skewed humoral immune activity. Therefore, we suggest that DMF, but not fingolimod, may exacerbate humoral immune imbalance and enhance autoantibody production, leading to aggravation of MOGAD.Entities:
Keywords: anti-myelin oligodendrocyte glycoprotein antibody-associated disease; dimethyl fumarate; fingolimod; multiple sclerosis; seroconversion
Year: 2021 PMID: 33659007 PMCID: PMC7917254 DOI: 10.3389/fimmu.2021.625465
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561