血栓性血小板减少性紫癜动物模型:叙述性综述

Annals of blood Pub Date : 2023-09-30 Epub Date: 2022-11-16 DOI:10.21037/aob-22-18
Liang Zheng, X Long Zheng
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引用次数: 0

摘要

背景和目的:血栓性血小板减少性紫癜(TTP)是一种潜在的致命性血液疾病,由血浆 ADAMTS13(具有血栓栓蛋白 1 型重复序列的崩解酶和金属蛋白酶,13)活性严重缺乏所致。ADAMTS13 通过蛋白水解作用裂解超大型冯-威廉因子(VWF),对正常止血至关重要。自 2001 年发现 ADAMTS13 以来,已建立了多个 TTP 动物模型。在这篇叙述性综述中,我们总结了迄今为止已建立的 TTP 动物模型的建立和特征:我们使用自由文本在 PubMed 上检索了 1969 年至 2022 年的文献:TTP和动物模型。我们找到了 67 篇同行评议文章,但只有 33 篇文章被纳入综述,34 篇未讨论 TTP 的文章被排除在外:目前已在小鼠、大鼠、狒狒和斑马鱼中建立了转基因或抗体介导的 TTP 模型,并对其进行了充分描述。然而,我们仍然迫切需要一种真正的自身免疫性 TTP 动物模型:这些动物模型使研究人员能够进一步评估各种潜在环境因素和/或遗传修饰因子对 TTP 发病、进展和结局的影响,并帮助评估预防和治疗遗传性和获得性 TTP 的新型方法的有效性和安全性。
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Animal models for thrombotic thrombocytopenic purpura: a narrative review.

Background and objective: Thrombotic thrombocytopenic purpura (TTP) is a potentially fatal blood disorder, resulting from severe deficiency of plasma ADAMTS13 (A Disintegrin And Metalloprotease with ThromboSpondin type 1 repeats, 13) activity. ADAMTS13 is crucial for normal hemostasis through proteolytic cleavage of ultra large von Willebrand factor (VWF). Since the discovery of ADAMTS13 in 2001, several animal models for TTP have been established. In this narrative review, we summarize the creation and characterization of the established animal models for TTP to date.

Methods: We performed a literature search through PubMed from 1969 to 2022 using free text: TTP and animal model. We found 67 peer-reviewed articles but only 33 articles were included for review and 34 articles that did not discuss TTP were excluded.

Key content and findings: There were genetically modified or antibody-mediated TTP models being established and fully characterized in mouse, rat, baboon, and zebrafish. However, we are still in urgent need of a true autoimmune TTP animal model.

Conclusions: These animal models allowed researchers to further evaluate the contribution of various potential environmental factors and/or genetic modifiers to the pathogenesis, progression, and outcome of TTP; and to help assess the efficacy and safety of novel approaches for prevention and treatment of both hereditary and acquired TTP.

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