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血栓性血小板减少性紫癜的动物模型:一项叙述性综述。

Animal models for thrombotic thrombocytopenic purpura: a narrative review.

作者信息

Zheng Liang, Zheng X Long

机构信息

Department of Pathology and Laboratory Medicine, The University of Kansas Medical Center, Kansas City, KS, USA.

出版信息

Ann Blood. 2023 Sep 30;8. doi: 10.21037/aob-22-18. Epub 2022 Nov 16.

Abstract

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.

摘要

背景与目的

血栓性血小板减少性紫癜(TTP)是一种潜在致命的血液疾病,由血浆中ADAMTS13(含Ⅰ型血小板反应蛋白基序的解聚素和金属蛋白酶13)活性严重缺乏所致。ADAMTS13通过对超大血管性血友病因子(VWF)进行蛋白水解切割,对正常止血至关重要。自2001年发现ADAMTS13以来,已建立了多种TTP动物模型。在这篇叙述性综述中,我们总结了迄今已建立的TTP动物模型的构建及特征。

方法

我们通过PubMed对1969年至2022年的文献进行检索,检索词为:TTP和动物模型。我们找到了67篇经同行评审的文章,但仅纳入33篇进行综述,排除34篇未讨论TTP的文章。

关键内容与发现

已在小鼠、大鼠、狒狒和斑马鱼中建立并全面表征了基因改造或抗体介导的TTP模型。然而,我们仍迫切需要一种真正的自身免疫性TTP动物模型。

结论

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/或基因修饰因子对TTP发病机制、进展和结局的影响;并有助于评估预防和治疗遗传性及获得性TTP新方法的疗效和安全性。

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