De Marco Gabriele, Giryes Sami, Williams Katie, Alcorn Nicola, Slade Maria, Fitton John, Nizam Sharmin, Smithson Gayle, Iqbal Khizer, Tran Gui, Pekarska Katrina, Keen Mansoor Ul Haq, Solaiman Mohammad, Middleton Edward, Wood Samuel, Buss Rihards, Devine Kirsty, Marzo-Ortega Helena, Green Mike, McGonagle Dennis Gerald
NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Chapel Allerton Hospital, Leeds LS7 4SA, UK.
Section of Experimental Rheumatology, The Leeds Institute for Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds LS7 4SA, UK.
Vaccines (Basel). 2022 Jul 26;10(8):1184. doi: 10.3390/vaccines10081184.
The novel SARS-CoV-2 vaccines partially exploit intrinsic DNA or RNA adjuvanticity, with dysregulation in the metabolism of both these nucleic acids independently linked to triggering experimental autoimmune diseases, including lupus and myositis.
Herein, we present 15 new onset autoimmune myositis temporally associated with SARS-CoV-2 RNA or DNA-based vaccines that occurred between February 2021 and April 2022. Musculoskeletal, pulmonary, cutaneous and cardiac manifestations, laboratory and imaging data were collected.
In total, 15 cases of new onset myositis (11 polymyositis/necrotizing/overlap myositis; 4 dermatomyositis) were identified in the Yorkshire region of approximately 5.6 million people, between February 2021 and April 2022 (10 females/5 men; mean age was 66.1 years; range 37-83). New onset disease occurred after first vaccination (5 cases), second vaccination (7 cases) or after the third dose (3 cases), which was often a different vaccine. Of the cases, 6 had systemic complications including skin (3 cases), lung (3 cases), heart (2 cases) and 10/15 had myositis associated autoantibodies. All but 1 case had good therapy responses. Adverse event following immunization (AEFI) could not be explained based on the underlying disease/co-morbidities.
Compared with our usual regional Rheumatology clinical experience, a surprisingly large number of new onset myositis cases presented during the period of observation. Given that antigen release inevitably follows muscle injury and given the role of nucleic acid adjuvanticity in autoimmunity and muscle disease, further longitudinal studies are required to explore potential links between novel coronavirus vaccines and myositis in comparison with more traditional vaccine methods.
新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗部分利用了内在的DNA或RNA佐剂活性,而这两种核酸代谢的失调均独立地与引发实验性自身免疫性疾病(包括狼疮和肌炎)有关。
在此,我们报告了2021年2月至2022年4月期间发生的15例与基于SARS-CoV-2 RNA或DNA的疫苗在时间上相关的新发自身免疫性肌炎病例。收集了肌肉骨骼、肺部、皮肤和心脏表现、实验室及影像学数据。
在约560万人口的约克郡地区,2021年2月至2022年4月期间共确诊15例新发肌炎病例(11例多发性肌炎/坏死性/重叠性肌炎;4例皮肌炎)(10名女性/5名男性;平均年龄66.1岁;范围37 - 83岁)。新发疾病发生在首次接种疫苗后(5例)、第二次接种疫苗后(7例)或第三次接种后(3例),且接种的疫苗通常不同。其中6例有全身并发症,包括皮肤(3例)、肺部(3例)、心脏(2例),15例中有10例有与肌炎相关的自身抗体。除1例病例外,其余所有病例对治疗反应良好。免疫接种后不良事件(AEFI)无法根据基础疾病/合并症来解释。
与我们地区常规的风湿病临床经验相比,在观察期间出现了数量惊人的新发肌炎病例。鉴于抗原释放不可避免地伴随肌肉损伤,且考虑到核酸佐剂活性在自身免疫和肌肉疾病中的作用,需要进一步开展纵向研究,以探索新型冠状病毒疫苗与肌炎之间的潜在联系,并与更传统的疫苗方法进行比较。