Department of Medicine, Michael G. DeGroote School of Medicine, McMaster University, Hamilton, Ontario, Canada.
Department of Medicine, Michael G. DeGroote School of Medicine, McMaster University, Hamilton, Ontario, Canada; McMaster Center for Transfusion Research, McMaster University, Hamilton, Ontario, Canada; Service of Benign Hematology, Department of Medicine, Hamilton Health Sciences, Hamilton, Ontario Canada.
Semin Hematol. 2022 Apr;59(2):89-96. doi: 10.1053/j.seminhematol.2022.03.002. Epub 2022 Mar 7.
Vaccine-induced immune thrombotic thrombocytopenia (VITT) is a novel prothrombotic disorder characterized by thrombosis, thrombocytopenia, and disseminated intravascular coagulation identified in hundreds of recipients of ChAdOx1 nCoV-19 (Oxford/AstraZeneca), an adenovirus vector coronavirus disease 2019 (COVID-19) vaccine. VITT resembles heparin-induced thrombocytopenia (HIT) in that patients have platelet-activating anti-platelet factor 4 antibodies; however, whereas heparin typically enhances platelet activation by HIT antibodies, VITT antibody-induced platelet activation is often inhibited in vitro by pharmacological concentrations of heparin. Further, the thrombotic complications in VITT feature much higher frequencies of atypical thrombosis, most notably cerebral vein thrombosis and splanchnic vein thrombosis, compared with HIT. In this review, we outline the treatments that have been used to manage this novel condition since its recognition in March 2021, including anticoagulation, high-dose intravenous immune globulin, therapeutic plasma exchange, corticosteroids, rituximab, and eculizumab. We discuss the controversial issue of whether heparin, which often inhibits VITT antibody-induced platelet activation, is harmful in the treatment of VITT. We also describe a case of "long VITT," describing the treatment challenges resulting from platelet-activating anti-PF4 antibodies that persisted for more than 9 months.
疫苗诱导的免疫性血栓性血小板减少症(VITT)是一种新型的促血栓形成性疾病,其特征为血栓形成、血小板减少和弥散性血管内凝血,已在数百名接种 ChAdOx1 nCoV-19(牛津/阿斯利康)疫苗的患者中发现,该疫苗是一种腺病毒载体 2019 年冠状病毒病(COVID-19)疫苗。VITT 类似于肝素诱导的血小板减少症(HIT),因为患者存在血小板激活的抗血小板因子 4 抗体;然而,肝素通常通过 HIT 抗体增强血小板激活,而 VITT 抗体诱导的血小板激活在体外常被肝素的药理浓度抑制。此外,与 HIT 相比,VITT 的血栓性并发症具有更高频率的非典型血栓形成,尤其是脑静脉血栓形成和内脏静脉血栓形成。在这篇综述中,我们概述了自 2021 年 3 月发现这种新型疾病以来,用于治疗这种疾病的方法,包括抗凝、大剂量静脉注射免疫球蛋白、治疗性血浆置换、皮质类固醇、利妥昔单抗和依库珠单抗。我们讨论了肝素是否有害的争议问题,肝素通常抑制 VITT 抗体诱导的血小板激活,肝素是否有害的争议问题,我们还描述了一例“长 VITT”病例,描述了血小板激活的抗 PF4 抗体持续超过 9 个月导致的治疗挑战。