PMID- 38270296 OWN - NLM STAT- MEDLINE DCOM- 20240126 LR - 20240206 IS - 2050-4527 (Electronic) IS - 2050-4527 (Linking) VI - 12 IP - 1 DP - 2024 Jan TI - Immunosuppressive therapy and COVID-19 infection in patients with NMOSD. PG - e1128 LID - 10.1002/iid3.1128 [doi] LID - e1128 AB - INTRODUCTION: To evaluate whether treated with immunosuppressants in neuromyelitis optica spectrum disorder (NMOSD) shows an effect on the severity and outcomes of COVID-19 Omicron variant. METHODS: This is a substudy of a single-center clinical trial involving human umbilical cord mesenchymal stem cells (hUC-MSCs) in NMOSD patients. NMOSD patients with hUC-MSCs treatment, NMOSD patients without hUC-MSCs treatment, and matched healthy controls (HC) were included. Demographic information, NMOSD-related clinical features, comorbidities, use of disease-modifying therapy, COVID-19 vaccination status, COVID-19 clinical features, COVID-19 clinical outcomes, and NMOSD-related disease activity were obtained through online questionnaires or phone calls. RESULTS: The majority of NMOSD patients received long-term treatment with mycophenolate mofetil (68.8%) or azathioprine (22.9%), and 50% received oral glucocorticoid. During the epidemic, 97.4% of NMOSD patients infected with COVID-19 had asymptomatic or mild forms, with only two patients (2.6%) requiring hospitalization. None of these patients required tracheal intubation or admission to the intensive care unit. Clinical symptoms were found to be more prevalent in HC groups. Additionally, the HC groups had higher fever-recorded temperatures. NMOSD patients who received hUC-MSCs treatment had shorter disease duration than patients who did not receive hUC-MSCs treatment. DISCUSSION: Immunosuppressant-treated patients with NMOSD have a similar risk of COVID-19 infection as the general population, but the disease duration is shorter and the clinical symptoms are less severe. Among our NMOSD patients who received hUC-MSCs treatment, COVID-19 outcomes were favorable, with no increased risk of severe COVID-19. Prospective studies on immunotherapies are needed to help determine best treatment practices. CI - (c) 2024 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. FAU - Choi, Un Wai AU - Choi UW AUID- ORCID: 0000-0002-5949-9526 AD - Department of Neurology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. FAU - Ai, Xiwen AU - Ai X AD - Department of Neurology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. FAU - Li, Hongyan AU - Li H AD - Department of Neurology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. FAU - Hao, Yong AU - Hao Y AD - Department of Neurology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. FAU - Yao, Xiaoying AU - Yao X AD - Department of Neurology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. FAU - Guan, Yangtai AU - Guan Y AD - Department of Neurology, Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. LA - eng GR - DLY201605/School of Medicine, Shanghai Jiao Tong University/ GR - 81771295/National Natural Science Foundation of China/ GR - 2020YFA0113100/Ministry of Science and Technology of the People's Republic of China/ PT - Journal Article PL - England TA - Immun Inflamm Dis JT - Immunity, inflammation and disease JID - 101635460 RN - 0 (COVID-19 Vaccines) RN - SARS-CoV-2 variants SB - IM MH - Humans MH - COVID-19 Vaccines MH - *Neuromyelitis Optica/therapy MH - Prospective Studies MH - *COVID-19/therapy MH - SARS-CoV-2 MH - Immunosuppression Therapy PMC - PMC10790678 OTO - NOTNLM OT - COVID-19 OT - human umbilical cord mesenchymal stem cell (hUC-MSC) OT - immunosuppressant OT - neuromyelitis optica spectrum disorder (NMOSD) COIS- The authors declare no conflict of interest. EDAT- 2024/01/25 12:42 MHDA- 2024/01/26 06:43 PMCR- 2024/01/16 CRDT- 2024/01/25 08:19 PHST- 2023/11/20 00:00 [revised] PHST- 2023/08/18 00:00 [received] PHST- 2023/11/24 00:00 [accepted] PHST- 2024/01/26 06:43 [medline] PHST- 2024/01/25 12:42 [pubmed] PHST- 2024/01/25 08:19 [entrez] PHST- 2024/01/16 00:00 [pmc-release] AID - IID31128 [pii] AID - 10.1002/iid3.1128 [doi] PST - ppublish SO - Immun Inflamm Dis. 2024 Jan;12(1):e1128. doi: 10.1002/iid3.1128.