More on the pathogenesis of thrombotic thrombocytopenic purpura. Comment on "Acquired thrombotic thrombocytopenic purpura without detectable anti-ADAMTS13 antibodies: a possible underlying autoimmune mechanism" and on "The different faces of thrombotic thrombocytopenic purpura".
作者信息
Peyvandi Flora
机构信息
Università degli Studi di Milano, Department of Pathophysiology and Transplantation, Milan, Italy; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Milan.
出版信息
Haematologica. 2025 Jun 1;110(6):1443-1444. doi: 10.3324/haematol.2024.287163. Epub 2025 Jan 30.
Abstract
摘要
相似文献
1
More on the pathogenesis of thrombotic thrombocytopenic purpura. Comment on "Acquired thrombotic thrombocytopenic purpura without detectable anti-ADAMTS13 antibodies: a possible underlying autoimmune mechanism" and on "The different faces of thrombotic thrombocytopenic purpura".血栓性血小板减少性紫癜发病机制的更多探讨。对《未检测到抗ADAMTS13抗体的获得性血栓性血小板减少性紫癜：一种可能的潜在自身免疫机制》及《血栓性血小板减少性紫癜的不同表现》的评论
Haematologica. 2025 Jun 1;110(6):1443-1444. doi: 10.3324/haematol.2024.287163. Epub 2025 Jan 30.
2
The third form of thrombotic thrombocytopenic purpura shows up again: what is it, does it even exist, how to find out? Comment on "Acquired thrombotic thrombocytopenic purpura without detectable anti-ADAMTS13 antibodies: a possible underlying autoimmune mechanism" and on "The different faces of thrombotic thrombocytopenic purpura".血栓性血小板减少性紫癜的第三种形式再次出现：它是什么，是否真的存在，如何查明？对《无可检测的抗ADAMTS13抗体的获得性血栓性血小板减少性紫癜：一种可能的潜在自身免疫机制》及《血栓性血小板减少性紫癜的不同表现》的评论
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Child-onset and adolescent-onset acquired thrombotic thrombocytopenic purpura with severe ADAMTS13 deficiency: a cohort study of the French national registry for thrombotic microangiopathy.儿童期和青少年期起病的获得性血栓性血小板减少性紫癜伴严重ADAMTS13缺乏症：法国全国血栓性微血管病登记处的一项队列研究
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Epidemiology and pathophysiology of adulthood-onset thrombotic microangiopathy with severe ADAMTS13 deficiency (thrombotic thrombocytopenic purpura): a cross-sectional analysis of the French national registry for thrombotic microangiopathy.伴有严重ADAMTS13缺乏的成人期血栓性微血管病（血栓性血小板减少性紫癜）的流行病学和病理生理学：法国全国血栓性微血管病登记处的横断面分析
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Multiple domains of ADAMTS13 are targeted by autoantibodies against ADAMTS13 in patients with acquired idiopathic thrombotic thrombocytopenic purpura.针对获得性特发性血栓性血小板减少性紫癜患者的 ADAMTS13 自身抗体靶向 ADAMTS13 的多个结构域。
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Acquired Thrombotic Thrombocytopenic Purpura Without Anti-ADAMTS13 Antibody Caused by Influenza A (H1N1) Virus Successfully Treated by Plasma Exchange: A Case Report.获得性血栓性血小板减少性紫癜无抗 ADAMTS13 抗体由甲型流感病毒 (H1N1) 成功治疗血浆置换：一例报告。
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Human neutrophil peptides and complement factor Bb in pathogenesis of acquired thrombotic thrombocytopenic purpura.人中性粒细胞肽和补体因子Bb在获得性血栓性血小板减少性紫癜发病机制中的作用
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Acquired thrombotic thrombocytopenic purpura without detectable anti-ADAMTS13 antibodies: a possible underlying autoimmune mechanism.获得性血栓性血小板减少性紫癜，抗ADAMTS13抗体检测不到：一种可能的潜在自身免疫机制
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A case of severe ADAMTS13 deficiency presenting as thrombotic thrombocytopenic purpura in pregnancy.一例以妊娠期血栓性血小板减少性紫癜为表现的严重ADAMTS13缺乏症病例。
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本文引用的文献
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The different faces of thrombotic thrombocytopenic purpura.血栓性血小板减少性紫癜的不同表现。
Haematologica. 2025 Jun 1;110(6):1245-1247. doi: 10.3324/haematol.2024.286504. Epub 2024 Nov 14.
2
Acquired thrombotic thrombocytopenic purpura without detectable anti-ADAMTS13 antibodies: a possible underlying autoimmune mechanism.获得性血栓性血小板减少性紫癜，抗ADAMTS13抗体检测不到：一种可能的潜在自身免疫机制
Haematologica. 2025 Jun 1;110(6):1368-1372. doi: 10.3324/haematol.2024.285391. Epub 2024 Sep 26.
3
Risk of relapse after SARS-CoV-2 vaccine in the Milan cohort of thrombotic thrombocytopenic purpura patients.米兰血栓性血小板减少性紫癜患者队列中接种SARS-CoV-2疫苗后的复发风险。
Haematologica. 2023 Nov 1;108(11):3152-3155. doi: 10.3324/haematol.2022.282478.
4
Thrombotic Thrombocytopenic Purpura: From 1972 to 2022 and Beyond.血栓性血小板减少性紫癜：从 1972 年到 2022 年及以后。
Semin Thromb Hemost. 2022 Nov;48(8):926-936. doi: 10.1055/s-0042-1749589. Epub 2022 Jul 6.
5
Acquired Thrombotic Thrombocytopenic Purpura Without Anti-ADAMTS13 Antibody Caused by Influenza A (H1N1) Virus Successfully Treated by Plasma Exchange: A Case Report.获得性血栓性血小板减少性紫癜无抗 ADAMTS13 抗体由甲型流感病毒 (H1N1) 成功治疗血浆置换：一例报告。
Am J Case Rep. 2021 Aug 2;22:e932251. doi: 10.12659/AJCR.932251.
6
The ADAMTS13-von Willebrand factor axis in COVID-19 patients.新冠病毒感染患者中的ADAMTS13-血管性血友病因子轴
J Thromb Haemost. 2021 Feb;19(2):513-521. doi: 10.1111/jth.15191. Epub 2020 Dec 18.
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ISTH guidelines for the diagnosis of thrombotic thrombocytopenic purpura.ISTH 血栓性血小板减少性紫癜诊断指南。
J Thromb Haemost. 2020 Oct;18(10):2486-2495. doi: 10.1111/jth.15006. Epub 2020 Sep 11.
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Open ADAMTS13, induced by antibodies, is a biomarker for subclinical immune-mediated thrombotic thrombocytopenic purpura.激活的 ADAMTS13，由抗体诱导，是亚临床免疫介导性血栓性血小板减少性紫癜的生物标志物。
Blood. 2020 Jul 16;136(3):353-361. doi: 10.1182/blood.2019004221.
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ADAMTS13-specific circulating immune complexes as potential predictors of relapse in patients with acquired thrombotic thrombocytopenic purpura.ADAMTS13特异性循环免疫复合物作为获得性血栓性血小板减少性紫癜患者复发的潜在预测指标。
Eur J Intern Med. 2017 Apr;39:79-83. doi: 10.1016/j.ejim.2016.11.003. Epub 2016 Nov 22.
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Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies.血栓性血小板减少性紫癜及相关血栓性微血管病术语标准化的共识。
J Thromb Haemost. 2017 Feb;15(2):312-322. doi: 10.1111/jth.13571. Epub 2017 Jan 30.
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