Clinical and immunological features of COVID‐19 in patients with anti‐MDA5 dermatomyositis during the omicron wave in Chongqing, China

皮肌炎 优势比 接种疫苗 内科学 MDA5型 效价 医学 置信区间 CD8型 抗体 免疫学 胃肠病学 生物 免疫系统 核糖核酸 基因 生物化学 RNA干扰
作者
Na Wu,Zhiwei Chen,Guanhua Zha,Zhiling Deng,Wenhan Huang,Dachuan Cai,Mingli Peng,Peng Hu,Lin Tang,Hong Ren
出处
期刊:Journal of Medical Virology [Wiley]
卷期号:96 (3) 被引量:1
标识
DOI:10.1002/jmv.29493
摘要

Abstract Patients with anti‐melanoma differentiation‐associated gene 5 (anti‐MDA5) dermatomyositis (DM) have a higher risk of coronavirus disease 2019 (COVID‐19) infection. In this longitudinal observational study, we aimed to investigate the clinical and immunological features of these patients after COVID‐19 infection. A total of 73 patients with anti‐MDA5 DM were recruited from the Second Affiliated Hospital of Chongqing Medical University during the Omicron wave epidemic. Clinical data were collected by questionnaire survey and electronic medical records. Blood samples were used to determine the immunity responses. From December 9, 2022 to March 31, 2023, 67 patients were eligible for final analysis; 68.7% of them were infected with COVID‐19. The most common symptoms observed in COVID‐19 were upper respiratory symptoms, most cases were mild or moderate (97.8%). The clinical laboratory indexes were relativity stable in patients after infection (all p > 0.05). Vaccination is not a protective factor against the Omicron infection (odds ratio: 2.69, 95% confidence interval: 0.81–8.93, p = 0.105). Both wildtype (WT) neutralizing antibodies titer and BA.5‐specific immunoglobulin G titer were significantly enhanced after infection (all p < 0.01), which was as high as healthy controls (HCs). The memory B‐cell responses were similar between the patients with anti‐MDA5 DM and HCs ( p > 0.05). However, both the WT‐specific CD8 + T cells and CD4 + T cells were reduced in patients with anti‐MDA5 DM (all p < 0.05). In conclusion, patients with anti‐MDA5 DM did not deteriorate the COVID‐19, in turn, COVID‐19 infection did not increase the risk of anti‐MDA5 DM exacerbation. The humoral responses were robust but the cellular responses were weakened after COVID‐19 infection.
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