Department of Pathophysiology, Ivano-Frankivsk National Medical University, Ivano-Frankivsk, Ukraine.
Department of Clinical Immunology and Rheumatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Rheumatol Int. 2023 Sep;43(9):1651-1664. doi: 10.1007/s00296-023-05345-y. Epub 2023 Jun 23.
Limited evidence on long-term COVID-19 vaccine safety in patients with idiopathic inflammatory myopathies (IIMs) continues to contribute to vaccine hesitancy. We studied delayed-onset vaccine adverse events (AEs) in patients with IIMs, other systemic autoimmune and inflammatory disorders (SAIDs), and healthy controls (HCs), using data from the second COVID-19 Vaccination in Autoimmune Diseases (COVAD) study. A validated self-reporting e-survey was circulated by the COVAD study group (157 collaborators, 106 countries) from Feb-June 2022. We collected data on demographics, comorbidities, IIM/SAID details, COVID-19 history, and vaccination details. Delayed-onset (> 7 day) AEs were analyzed using regression models. A total of 15165 respondents undertook the survey, of whom 8759 responses from vaccinated individuals [median age 46 (35-58) years, 74.4% females, 45.4% Caucasians] were analyzed. Of these, 1390 (15.9%) had IIMs, 50.6% other SAIDs, and 33.5% HCs. Among IIMs, 16.3% and 10.2% patients reported minor and major AEs, respectively, and 0.72% (n = 10) required hospitalization. Notably patients with IIMs experienced fewer minor AEs than other SAIDs, though rashes were expectedly more than HCs [OR 4.0; 95% CI 2.2-7.0, p < 0.001]. IIM patients with active disease, overlap myositis, autoimmune comorbidities, and ChadOx1 nCOV-19 (Oxford/AstraZeneca) recipients reported AEs more often, while those with inclusion body myositis, and BNT162b2 (Pfizer) recipients reported fewer AEs. Vaccination is reassuringly safe in individuals with IIMs, with AEs, hospitalizations comparable to SAIDs, and largely limited to those with autoimmune multimorbidity and active disease. These observations may inform guidelines to identify high-risk patients warranting close monitoring in the post-vaccination period.
在特发性炎性肌病(IIM)患者中,关于 COVID-19 疫苗长期安全性的证据有限,这仍然导致了疫苗犹豫。我们使用来自第二次自身免疫性疾病 COVID-19 疫苗接种(COVAD)研究的数据,研究了 IIM 患者、其他系统性自身免疫和炎症性疾病(SAID)患者以及健康对照者(HC)的迟发性疫苗不良反应(AE)。COVAD 研究小组(157 名合作者,来自 106 个国家)于 2022 年 2 月至 6 月间通过一份经过验证的自我报告电子调查进行了调查。我们收集了人口统计学、合并症、IIM/SAID 详细信息、COVID-19 病史和疫苗接种详细信息。使用回归模型分析迟发性(>7 天)AE。共有 15165 名受访者参与了这项调查,其中 8759 名接种疫苗者的应答(中位年龄 46[35-58]岁,74.4%为女性,45.4%为白种人)被分析。其中,1390 人(15.9%)患有 IIM,50.6%患有其他 SAID,33.5%为 HC。在 IIM 患者中,分别有 16.3%和 10.2%的患者报告了轻微和严重 AE,0.72%(n=10)需要住院治疗。值得注意的是,与其他 SAID 相比,患有 IIM 的患者经历的轻微 AE 更少,而皮疹比 HC 更常见[比值比 4.0;95%置信区间 2.2-7.0,p<0.001]。患有活动性疾病、重叠性肌炎、自身免疫合并症和接受 ChadOx1 nCOV-19(牛津/阿斯利康)的 IIM 患者更常报告 AE,而患有包涵体肌炎和接受 BNT162b2(辉瑞)的患者报告的 AE 较少。在 IIM 患者中,疫苗接种是安全的,AE 和住院率与 SAID 相当,且主要局限于自身免疫性多合并症和活动性疾病患者。这些观察结果可能为指导方针提供信息,以确定需要在接种疫苗后密切监测的高危患者。