UOC di Gastroenterologia, Dipartimento di Scienze Mediche e Chirurgiche, Fondazione Policlinico Universitario A. Gemelli IRCCS, L. go A. Gemelli 8, Roma, Italia.
Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, L. go F. Vito 1, Roma, Italia.
Intern Emerg Med. 2024 Jan;19(1):13-37. doi: 10.1007/s11739-023-03366-w. Epub 2023 Jul 27.
Henoch-Schonlein purpura (HSP) is an IgA-mediated systemic small-vessel vasculitis (IgAV) that typically presents with a variable tetrad of symptoms. HSP if often preceded by respiratory tract infections, vaccinations, drugs or malignancies. During the recent COVID-19 pandemic multiples cases of HSP have been described after both infection and vaccination for SARS-CoV2. This study aims to perform a systematic review of literature and describe an additional complicated case of de-novo HSP appeared after the administration of the third dose of a mRNA-SARS-CoV2 vaccination.
Electronic bibliographic research was performed to identify all the original reports describing cases of de-novo HSP or IgAV appeared after respiratory infection or vaccine administration for SARS-CoV2. We included all case series or case reports of patients who respected our inclusion and exclusion criteria.
Thirty-eight publications met our pre-defined inclusion criteria, for an overall number of 44 patients. All patients presented with palpable purpura variable associated with arthralgia, abdominal pain or renal involvement. Increased levels of inflammation markers, mild leukocytosis and elevated D-dimer were the most common laboratory findings. Up to 50% of patients presented proteinuria and/or hematuria. Almost all skin biopsies showed leukocytoclastic vasculitis, with IgA deposits at direct immunofluorescence in more than 50% of cases.
Our results suggest that the immune response elicited by SARS-CoV2 vaccine or infection could play a role in the development of HSP. Current research suggests a possible role of IgA in immune hyperactivation, highlighted by early seroconversion to IgA found in some COVID-19 patients who develop IgA vasculitis.
过敏性紫癜(HSP)是一种 IgA 介导的系统性小血管血管炎(IgAV),通常表现为症状多变的四联征。HSP 常以前呼吸道感染、疫苗接种、药物或恶性肿瘤为前驱。在最近的 COVID-19 大流行期间,描述了多种在 SARS-CoV2 感染和疫苗接种后出现 HSP 的病例。本研究旨在进行文献系统回顾,并描述在接种第三剂 mRNA-SARS-CoV2 疫苗后出现的新发性 HSP 的复杂病例。
进行电子文献检索,以确定所有描述呼吸道感染或 SARS-CoV2 疫苗接种后出现新发性 HSP 或 IgAV 的原始病例报告。我们纳入了符合纳入和排除标准的所有患者的病例系列或病例报告。
符合我们预先定义的纳入标准的有 38 篇文献,共纳入 44 例患者。所有患者均表现为可触及紫癜,伴有关节痛、腹痛或肾受累的多变性。炎症标志物升高、轻度白细胞增多和升高的 D-二聚体是最常见的实验室发现。多达 50%的患者出现蛋白尿和/或血尿。几乎所有皮肤活检均显示白细胞碎裂性血管炎,直接免疫荧光检查中超过 50%的病例有 IgA 沉积。
我们的结果表明,SARS-CoV2 疫苗或感染引起的免疫反应可能在 HSP 的发病机制中起作用。目前的研究表明,IgA 在免疫过度激活中可能发挥作用,这一点在一些发生 IgA 血管炎的 COVID-19 患者中表现为早期 IgA 血清转化。