Leung Wing-Yin, Wu Henry H L, Floyd Lauren, Ponnusamy Arvind, Chinnadurai Rajkumar
Department of Renal Medicine, Lancashire Teaching Hospitals NHS Foundation Trust, Preston PR2 9HT, UK.
Renal Research Laboratory, Kolling Institute of Medical Research, Royal North Shore Hospital & The University of Sydney, Sydney, NSW 2065, Australia.
Vaccines (Basel). 2023 Jun 24;11(7):1139. doi: 10.3390/vaccines11071139.
Amyloidosis is a complex disorder characterized by deposited insoluble fibrillar proteins which misfold into β-pleated sheets. The pathogenesis of amyloidosis can vary but can be the result of immune dysregulation that occurs from sustained high inflammatory states, often known as AA amyloidosis. Multi-organ involvement including hepatic, gastrointestinal, renal, cardiac and immunological pathological manifestations has been observed amongst individuals presenting with amyloidosis. The recent global pandemic of severe acute respiratory syndrome coronavirus 2, also referred to as coronavirus 2019 (COVID-19), has been shown to be associated with multiple health complications, many of which are similar to those seen in amyloidosis. Though COVID-19 is recognized primarily as a respiratory disease, it has since been found to have a range of extra-pulmonary manifestations, many of which are observed in patients with amyloidosis. These include features of oxidative stress, chronic inflammation and thrombotic risks. It is well known that viral illnesses have been associated with the triggering of autoimmune conditions of which amyloidosis is no different. Over the recent months, reports of new-onset and relapsed disease following COVID-19 infection and vaccination have been published. Despite this, the exact pathophysiological associations of COVID-19 and amyloidosis remain unclear. We present a scoping review based on our systematic search of available evidence relating to amyloidosis, COVID-19 infection and COVID-19 vaccination, evaluating current perspectives and providing insight into knowledge gaps that still needs to be addressed going forward.
淀粉样变性是一种复杂的疾病,其特征是沉积不溶性纤维状蛋白质,这些蛋白质错误折叠成β-折叠片层。淀粉样变性的发病机制可能各不相同,但可能是持续高炎症状态导致的免疫失调的结果,通常称为AA型淀粉样变性。在患有淀粉样变性的个体中,已观察到多器官受累,包括肝脏、胃肠道、肾脏、心脏和免疫病理表现。最近全球范围内的严重急性呼吸综合征冠状病毒2大流行,也称为冠状病毒病2019(COVID-19),已被证明与多种健康并发症有关,其中许多与淀粉样变性中所见的并发症相似。尽管COVID-19主要被认为是一种呼吸道疾病,但后来发现它有一系列肺外表现,其中许多在淀粉样变性患者中也有观察到。这些表现包括氧化应激、慢性炎症和血栓形成风险的特征。众所周知,病毒感染与自身免疫性疾病的触发有关,淀粉样变性也不例外。在最近几个月里,已经发表了关于COVID-19感染和疫苗接种后新发和复发疾病的报告。尽管如此,COVID-19与淀粉样变性的确切病理生理关联仍不清楚。我们基于对与淀粉样变性、COVID-19感染和COVID-19疫苗接种相关的现有证据的系统搜索,进行了一项范围综述,评估当前观点,并深入了解仍需解决的知识空白。