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Long-term efficacy of mycophenolate mofetil in myelin oligodendrocyte glycoprotein antibody-associated disorders: A prospective study
Open accessAbstract
OBJECTIVE: To investigate whether the use of mycophenolate mofetil (MMF) could reduce the relapse risk in patients with myelin oligodendrocyte glycoprotein (MOG)-immunoglobulin G (IgG)-associated disorders (MOGADs). METHODS: This prospective observational cohort study included patients with MOGAD at Peking Union Medical College Hospital between January 1, 2017, and April 30, 2019. The patients were divided into 2 groups: those with (MMF+) or without (MMF-) MMF therapy. The primary outcome was relapse at follow-up. We used Cox proportional hazards models to calculate hazard ratios (HRs) for relapse. RESULTS: Seventy-nine patients were included in our MOG cohort. Fifty (63.3%) were adults at index date, and 47 (59.5%) were women. Fifty-four (68.4%) were in the MMF+ group, and 25 (31.6%) were in the MMF- group. Clinical and demographic factors, MOG-IgG titer, and follow-up time (median, 472.5 days for MMF+, 261.0 days for MMF-) were comparable between the groups. Relapse rates were 7.4% (4/54) in the MMF+ group and 44.0% (11/25) in the MMF- group. Of all potential confounders, only the use of MMF was associated with reduced risk of relapse. The HR for relapse among patients in the MMF+ group was 0.14 (95% CI, 0.05-0.45) and was 0.08 (95% CI, 0.02-0.28) in a model adjusted for age, sex, disease course, and MOG-IgG titer. MMF therapy also remained associated with a reduced relapse risk in sensitivity analyses. Only one patient (1.9%) discontinued MMF therapy because of adverse effect. CONCLUSIONS: These findings provide a clinical evidence that MMF immunosuppression therapy may prevent relapse in patients with MOGAD. CLASSIFICATION OF EVIDENCE: This study provides class IV evidence that for patients with MOGAD, MMF reduces relapse risk.
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“In any case, the long-term persistence of (re-)activatable autoantigen-specific ThEx cells in patients in remission may well explain the less-than-perfect treatment efficacy of steroid-sparing agents, 64-67 depletion of CD19/CD20 memory B cells, 68,69 as well as exacerbation of disease by b -IFN. 27,70”
From Autoantigen-specific CD4+ T cells acquire an exhausted phenotype and persist in human antigen-specific autoimmune diseases (2024) · cites this paper as [65]
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Metadata
- Authors
- Li, S., Ren, H., Xu, Y., Xu, T., Zhang, Y., Yin, H., Zhang, W., Li, J., Ren, X., Fang, F., Li, W., Zhu, Y., Peng, B., Wang, J., Zhong, Y., & Cui, L.
- Affiliations
- Capital Medical University (CN)
- From the Department of Neurology (S.L., H.R., Y.X., Y. Zhang, H.Y., Y. Zhu, B.P., L.C.), Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences; Department of Epidemiology and Biostatistics Institute of Basic Medical Sciences (T.X.), Chinese Academy of Medical Sciences & School of Basic Medicine, Peking Union Medical College; Department of Neurology (W.Z., J.L., X.R., F.F.), Beijing Children's Hospital, Capital Medical University, National...
- Corresponding author
- Xu, Yan
- Xu, Tao
- ORCID
- Venue
- Neurology Neuroimmunology & Neuroinflammation
- Published
- 2020-05
- Volume
- 7
- Issue
- 3
- ISSN
- 2332-7812 (ISSN-L)
- PMC
- PMC7136046
- OpenAlex
- W3011563890
- Cited by
- 66
- References
- 34
- Citations by year
- 2026: 6 · 2025: 4 · 2024: 12 · 2023: 4 · 2022: 10 · 2021: 17 · 2020: 12
- FWCI
- 7.07
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by-nc-nd
- Locations
- Neurology Neuroimmunology & Neuroinflammation (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- Peking Union Medical College Hospital
- Peking Union Medical College
- National Key Research and Development Program of China (No.2016YFC0901500, [2016YFC0901500])
- Topics
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Health Sciences › Medicine › Clinical Neurology › Peripheral Neuropathies and Disorders
- Health Sciences › Medicine › Clinical Neurology › Autoimmune Neurological Disorders and Treatments
- Keywords
- mycophenolate mofetil, anti-MOG antibodies, relapse prevention, immunosuppressive therapy, relapse risk, demyelinating disease, long-term efficacy, treatment discontinuation
- MeSH terms
- Adolescent, Adult, Child, Drug Therapy, Combination, Female, Follow-Up Studies, Glucocorticoids, Humans, Immunoglobulin G, Immunologic Factors, Male, Mycophenolic Acid, Prospective Studies, Recurrence, Proportional Hazards Models, Outcome Assessment, Health Care, Demyelinating Autoimmune Diseases, CNS, Secondary Prevention, Young Adult, Myelin-Oligodendrocyte Glycoprotein
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- Li, S., Ren, H., Xu, Y., Xu, T., Zhang, Y., Yin, H., Zhang, W., Li, J., Ren, X., Fang, F., Li, W., Zhu, Y., Peng, B., Wang, J., Zhong, Y., & Cui, L. (2020). Long-term efficacy of mycophenolate mofetil in myelin oligodendrocyte glycoprotein antibody-associated disorders: A prospective study. Neurology Neuroimmunology & Neuroinflammation. https://doi.org/10.1212/nxi.0000000000000705