Platelet activating histone/antihistone IgG complexes in anti-PF4 negative thrombosis and thrombocytopenia syndrome.

IF 7.4 1区 医学 Q1 HEMATOLOGY
Max Esefeld, Stefan Handtke, Rainer Kaiser, Leo Nicolai, Lea Di Fina, Dario Rossaro, Jan Wesche, Justina Rath, Ann-Christin Wienrich, Till Hoffmann, Lukas Harasser, Clemens Feistritzer, Lorin Loacker, Kourosh Lotfi, Margareta Holmström, Jovan Antovic, Leif Steil, Uwe Volker, Lena Ulm, Karsten Becker, Nils-Olaf Hübner, Andreas Greinacher, Thomas Thiele
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引用次数: 0

Abstract

Thrombosis and Thrombocytopenia syndromes (TTS) describe immune mediated thrombotic adverse reactions following vaccination against Covid-19. Vaccine-induced immune thrombotic thrombocytopenia (VITT) is a well-known sub-entity of TTS, caused by adenovirus vector-based vaccines. VITT is mediated by anti-platelet factor 4 (PF4) IgG-antibodies, activating platelets via Fc-gamma IIa receptors (FcgRIIa). We describe clinical and serological features of 18 patients with anti-PF4/heparin ELISA negative TTS in temporal relationship to mRNA-based Covid-19 vaccination. Symptoms began at a median of 7 (range 1-61) days after vaccination. Patients showed thrombocytopenia (59,000/µl, 0-127,000/µl); petechiae (n=7), venous thromboembolism (n=11), arterial thrombosis (n=6), disseminated intravascular coagulation (n=1), and combined arterial and venous thromboses (n=1). Twelve sera induced FcgRIIa dependent and caspase independent procoagulant activation of platelets indicated by phosphatidylserine exposure and CD62P expression. We found histones precipitated with IgG fractions of TTS sera and antibodies binding to histones were found in 8/12 platelet-activating sera. Ex vivo generated histone/anti-histone IgG complexes strongly activated platelets via FcgRIIa, whereas anti-histone-IgG alone did not. Platelet autoantibodies were detected in 7/12 sera targeting GPIIb/IIIa (n=5); GPIb/IX (n=5) and GPIa/IIa (n=3). However, sera containing platelet anti-GPIIb/IIIa autoantibodies activated also platelets from a Glanzmann patient, making it unlikely that these autoantibodies are causative for platelet activation. Finally, 2/114 healthy vaccinees developed anti-histone antibodies after mRNA-based Covid-19 vaccination. Our data indicate a new sub-entity of TTS associated with platelet activating histone/anti-histone IgG complexes. Further studies are warranted to characterize the biological and clinical role of post-mRNA-based vaccination anti-histone antibodies. SeCo, NCT04370119.

血栓和血小板减少综合征(TTS)是指接种 Covid-19 疫苗后出现的免疫介导的血栓性不良反应。疫苗诱导的免疫性血栓性血小板减少症(VITT)是由腺病毒载体疫苗引起的一种众所周知的 TTS 子症状。VITT 由抗血小板因子 4 (PF4) IgG 抗体介导,通过 Fc-gamma IIa 受体 (FcgRIIa) 激活血小板。我们描述了 18 名抗 PF4/肝素 ELISA 阴性 TTS 患者的临床和血清学特征与基于 mRNA 的 Covid-19 疫苗接种的时间关系。症状开始于接种疫苗后的中位数 7 天(1-61 天)。患者出现血小板减少(59,000/µl,0-127,000/µl)、瘀斑(7 例)、静脉血栓栓塞(11 例)、动脉血栓(6 例)、弥散性血管内凝血(1 例)以及动脉和静脉血栓合并(1 例)。12 种血清诱导血小板的 FcgRIIa 依赖性和 caspase 独立性促凝活化,表现为磷脂酰丝氨酸暴露和 CD62P 表达。我们发现组蛋白与TTS血清中的IgG馏分沉淀在一起,并且在8/12种血小板活化血清中发现了与组蛋白结合的抗体。体内外生成的组蛋白/抗组蛋白IgG复合物可通过FcgRIIa强烈激活血小板,而单独的抗组蛋白IgG则不能。7/12的血清中检测到了针对GPIIb/IIIa(n=5)、GPIb/IX(n=5)和GPIa/IIa(n=3)的血小板自身抗体。然而,含有血小板抗 GPIIb/IIIa 自身抗体的血清也激活了一名格兰兹曼患者的血小板,因此这些自身抗体不太可能是激活血小板的原因。最后,2/114 名健康接种者在接种基于 mRNA 的 Covid-19 疫苗后产生了抗组蛋白抗体。我们的数据表明,与血小板活化组蛋白/抗组蛋白IgG复合物相关的TTS是一个新的亚实体。有必要进一步研究基于mRNA的疫苗接种后抗组蛋白抗体的生物学和临床作用。SeCo,NCT04370119。
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来源期刊
Blood advances
Blood advances Medicine-Hematology
CiteScore
12.70
自引率
2.70%
发文量
840
期刊介绍: Blood Advances, a semimonthly medical journal published by the American Society of Hematology, marks the first addition to the Blood family in 70 years. This peer-reviewed, online-only, open-access journal was launched under the leadership of founding editor-in-chief Robert Negrin, MD, from Stanford University Medical Center in Stanford, CA, with its inaugural issue released on November 29, 2016. Blood Advances serves as an international platform for original articles detailing basic laboratory, translational, and clinical investigations in hematology. The journal comprehensively covers all aspects of hematology, including disorders of leukocytes (both benign and malignant), erythrocytes, platelets, hemostatic mechanisms, vascular biology, immunology, and hematologic oncology. Each article undergoes a rigorous peer-review process, with selection based on the originality of the findings, the high quality of the work presented, and the clarity of the presentation.
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