Dainese Cristina, Valeri Federica, Bruno Benedetto, Borchiellini Alessandra
Regional Centre for Hemorrhagic and Thrombotic Diseases, AOU Città Della Salute e Della Scienza, 10126 Turin, Italy.
Division of Hematology, AOU Città Della Salute e Della Scienza and University of Turin, 10124 Turin, Italy.
J Clin Med. 2023 Aug 29;12(17):5630. doi: 10.3390/jcm12175630.
Thrombotic thrombocytopenic purpura (TTP) is a fatal disease in which platelet-rich microthrombi cause end-organ ischemia and damage. TTP is caused by markedly reduced ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13) activity. ADAMTS13 autoantibodies (autoAbs) are the major cause of immune TTP (iTTP), determining ADAMTS13 deficiency. The pathophysiology of such autoAbs as well as their prognostic role are continuous objects of scientific studies in iTTP fields. This review aims to provide clinicians with the basic information and updates on autoAbs' structure and function, how they are typically detected in the laboratory and their prognostic implications. This information could be useful in clinical practice and contribute to future research implementations on this specific topic.
血栓性血小板减少性紫癜(TTP)是一种致命性疾病,富含血小板的微血栓会导致终末器官缺血和损伤。TTP是由ADAMTS13(具有血小板反应蛋白-1基序的解整合素和金属蛋白酶13)活性显著降低引起的。ADAMTS13自身抗体(autoAbs)是免疫性TTP(iTTP)的主要病因,导致ADAMTS13缺乏。此类自身抗体的病理生理学及其预后作用一直是iTTP领域科学研究的对象。本综述旨在为临床医生提供关于自身抗体的结构和功能、在实验室中通常如何检测以及其预后意义的基本信息和最新进展。这些信息在临床实践中可能有用,并有助于未来针对这一特定主题的研究实施。