Department of Emergency and Disaster Medicine, Juntendo University Graduate School of Medicine, 2-1-1 Hongo Bunkyo-Ku, Tokyo 113-8421, Japan.
Departments of Anesthesiology, Critical Care, and Surgery, Duke University School of Medicine, Durham, NC, USA.
Trends Cardiovasc Med. 2022 Jul;32(5):249-256. doi: 10.1016/j.tcm.2022.02.008. Epub 2022 Feb 22.
Thrombosis that occurs in coronavirus disease 19 (COVID-19) is a serious complication and a critical aspect of pathogenesis in the disease progression. Although thrombocytopenia is uncommon in the initial presentation, it may also reflect disease severity due to the ability of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to activate platelets. This occurs directly through the spike protein-angiotensin converting enzyme 2 (ACE2) interaction and indirectly by coagulation and inflammation activation. Dysregulation in both innate and adaptive immune systems is another critical factor that causes thrombosis and thrombocytopenia in COVID-19. Vaccination is the most potent and effective tool to mitigate COVID-19; however, rare side effects, namely vaccine-induced immune thrombotic thrombocytopenia (VITT)/thrombosis with thrombocytopenia syndrome (TTS) can occur following adenovirus-vectored vaccine administration. VITT/TTS is rare, and thrombocytopenia can be the clue to detect this serious complication. It is important to consider that thrombocytopenia and/or thromboembolism are not events limited to post-vaccination with vectored vaccine, but are also seen rarely after vaccination with other vaccines. Various conditions mimic VITT/TTS, and it is vital to achieving the correct diagnosis at an earlier stage. Antiplatelet factor 4 (PF4) antibody detection by the enzyme-linked immunosorbent assay (ELISA) is used for diagnosing VITT/TTS. However, false-positive rates also occur in vaccinated people, who do not show any thrombosis or thrombocytopenia. Vaccinated people with messenger RNA vaccine can show positive but low density and non-functional in terms of platelet aggregation, it is vital to check the optical density. If anti-PF4 ELISA is not available, discriminating other conditions such as antiphospholipid syndrome, thrombotic thrombocytopenic purpura, immune thrombocytopenic purpura, systemic lupus erythematosus, and hemophagocytic syndrome/hemophagocytic lymphohistiocytosis is critical when the patients show thrombosis with thrombocytopenia after COVID-19 vaccination.
在 2019 冠状病毒病(COVID-19)中发生的血栓形成是一种严重的并发症,也是疾病进展中发病机制的一个关键方面。尽管血小板减少症在初始表现中并不常见,但由于严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)能够激活血小板,它也可能反映疾病的严重程度。这种情况既可以通过刺突蛋白-血管紧张素转换酶 2(ACE2)相互作用直接发生,也可以通过凝血和炎症激活间接发生。固有和适应性免疫系统的失调是导致 COVID-19 中血栓形成和血小板减少症的另一个关键因素。疫苗接种是减轻 COVID-19 的最有效和最有力的工具;然而,在接种腺病毒载体疫苗后,可能会发生罕见的副作用,即疫苗诱导的免疫性血栓性血小板减少症(VITT)/血小板减少性血栓形成综合征(TTS)。VITT/TTS 较为罕见,血小板减少症可能是发现这种严重并发症的线索。重要的是要认识到,血小板减少症和/或血栓栓塞并不是仅限于接种载体疫苗后的事件,在接种其他疫苗后也很少见。各种情况都可模拟 VITT/TTS,因此尽早做出正确诊断至关重要。酶联免疫吸附试验(ELISA)检测抗血小板因子 4(PF4)抗体用于诊断 VITT/TTS。然而,在接种疫苗的人群中也会出现假阳性率,这些人群没有任何血栓形成或血小板减少症。接种信使 RNA 疫苗的人群可能会出现阳性但密度低且在血小板聚集方面无功能的情况,因此检查光密度至关重要。如果没有抗 PF4 ELISA,在 COVID-19 疫苗接种后出现血栓形成伴血小板减少症的患者中,区分其他情况(如抗磷脂综合征、血栓性血小板减少性紫癜、免疫性血小板减少性紫癜、系统性红斑狼疮和噬血细胞综合征/噬血细胞性淋巴组织细胞增多症)至关重要。