Department of Microbiology, Immunology and Transplantation, Nephrology and Renal Transplantation Research Group, KU Leuven, Leuven, Belgium; Department of Nephrology and Renal Transplantation, UZ Leuven, Leuven, Belgium.
Departments of Laboratory Medicine, Imelda Hospital, Bonheiden, Belgium.
Am J Kidney Dis. 2023 Mar;81(3):364-367. doi: 10.1053/j.ajkd.2022.07.012. Epub 2022 Sep 19.
Atypical hemolytic uremic syndrome (aHUS) is a subtype of thrombotic microangiopathy (TMA) characterized by a dysregulation of the alternative complement pathway. Here, we report a previously healthy 38-year-old woman in whom aHUS developed after a COVID-19 vaccine booster. One day after receipt of a booster dose of mRNA-1273 vaccine, she felt ill. Because of persistent headache, nausea, and general malaise, she went to her general practitioner, who referred her to the hospital after detecting hypertension and acute kidney injury. A diagnosis of TMA was made. Her treatment consisted of blood pressure control, hemodialysis, plasma exchange, and respiratory support. Kidney biopsy confirmed the diagnosis of acute TMA. The patient was referred for treatment with eculizumab, and kidney function improved after initiation of this therapy. Genetic analysis revealed a pathogenic C3 variant. SARS-CoV-2 infection as a trigger for complement activation and development of aHUS has been described previously. In addition, there is one reported case of aHUS occurring after receipt of the adenovirus-based COVID-19 vaccine ChAdOx1 nCoV-19, but, to our knowledge, this is the first case of aHUS occurring after a booster dose of an mRNA COVID-19 vaccine in a patient with an underlying pathogenic variant in complement C3. Given the time frame, we hypothesize that the vaccine probably was the trigger for development of aHUS in this patient.
非典型溶血尿毒症综合征(aHUS)是血栓性微血管病(TMA)的一种亚型,其特征是补体替代途径失调。在这里,我们报告了一例先前健康的 38 岁女性,在接种 COVID-19 疫苗加强针后发生了 aHUS。在接种 mRNA-1273 疫苗加强针后一天,她感到不适。由于持续头痛、恶心和全身不适,她去看了全科医生,全科医生在检测到高血压和急性肾损伤后将她转至医院。诊断为 TMA。她的治疗包括控制血压、血液透析、血浆置换和呼吸支持。肾活检证实了急性 TMA 的诊断。患者被转介接受依库珠单抗治疗,在开始该治疗后肾功能得到改善。基因分析显示存在致病性 C3 变异。先前已经描述了 SARS-CoV-2 感染作为补体激活和 aHUS 发展的触发因素。此外,有一例报告的 aHUS 发生在接受基于腺病毒的 COVID-19 疫苗 ChAdOx1 nCoV-19 后,但据我们所知,这是首例在补体 C3 存在潜在致病性变异的患者中,接种 mRNA COVID-19 疫苗加强针后发生 aHUS 的病例。鉴于时间框架,我们假设疫苗可能是该患者发生 aHUS 的诱因。