重症肌无力
CD8型
医学
胃肠病学
队列
内科学
前瞻性队列研究
免疫系统
外围设备
病理生理学
免疫学
作者
Xiao Huan,Jialin Chen,Huahua Zhong,Yafang Xu,Yuan Wang,Haoqin Jiang,Jie Song,Chong Yan,Jianying Xi,Zhang‐Yu Zou,Jianming Zheng,Zhe Ruan,Song Tan,Lijun Luo,Sushan Luo,Chongbo Zhao
标识
DOI:10.1016/j.clim.2023.109879
摘要
The impact of Omicron infections on the clinical outcome and immune responses of myasthenia gravis (MG) remained largely unknown. From a prospective multicenter MG cohort (n = 189) with 197 myasthenic crisis (MC), we finally included 41 independent MG patients to classify into two groups: the Omicron Group (n = 13) and the Control Group (n = 28). In this matched cohort study, all-cause mortality was 7.69% (1/13) in Omicron Group and 14.29% (4/28) in Control Group. A higher proportion of elevated serum IL-6 was identified in the Omicron Group (88.89% vs 52.38%, P = 0.049). In addition, the proportions of CD3+CD8+T in lymphocytes and Tregs in CD3+CD4+ T cells were significantly elevated in the Omicron Group (both P = 0.0101). After treatment, the Omicron Group exhibited a marked improvement in MG-ADL score (P = 0.026) and MG-QoL-15 (P = 0.0357). MCs with Omicron infections were associated with elevated serum IL-6 and CD3+CD8+T response. These patients tended to present a better therapeutic response after fast-acting therapies and anti-IL-6 treatment.
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