Myelin oligodendrocyte glycoprotein antibody-associated disease in a patient with AIRE gene dominant-negative mutation
Myelin oligodendrocyte glycoprotein antibody–associated disease is a demyelinating disorder affecting the central nervous system. Autoimmune regulator mutations disrupt central tolerance and cause immunodeficiency and autoimmune manifestations. We report the case of a 49-year-old Asian male with relapsing myelin oligodendrocyte glycoprotein antibody–associated disease and a heterozygous dominant-negative autoimmune regulator mutation (c.901G > A, p.Val301Met), alongside vitiligo, cryptococcal disease and nasopharyngeal carcinoma. This case raises a potential link between negative selection failure and myelin oligodendrocyte glycoprotein antibody–associated disease and suggests that autoreactive T cells may be primary pathogenetic drivers, implying that restoring immune tolerance could inform future therapeutic approaches.
Authors
- Jiahao Lin (ORCID: https://orcid.org/0009-0000-8257-2595)
- Hu XueQiang
- Jingqi Wang (ORCID: https://orcid.org/0000-0001-6244-4932)
- Linling Wang
- Xiaonan Zhong (ORCID: https://orcid.org/0000-0001-9853-012X)
- Ruiwen Hu
- Rui Li
- Wei Qiu
- Lei Chen
- Tingting Lu
Institutions
- The University of Western Australia (AU)
- Changhai Hospital (CN)
- Perron Institute for Neurological and Translational Science (AU)
- Third Affiliated Hospital of Sun Yat-sen University (CN)
Publication Details
- Journal
- Multiple Sclerosis Journal
- Published
- 2026-10-08
- DOI
- https://doi.org/10.1177/13524585261490277
- Primary Topic
- Multiple Sclerosis Research Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00