中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Potent and rapid reversal of the von Willebrand factor inhibitor aptamer BT200

文献类型:期刊论文

作者Zhu, Shuhao4; Gilbert, James C.4; Liang, Zicai3; Kang, Daiwu3; Li, Ming1; Tarantino, Paul M.2; Jilma, Bernd5
刊名JOURNAL OF THROMBOSIS AND HAEMOSTASIS
出版日期2020-06-10
页码10
关键词glycoprotein Ib platelet reversal agent thrombosis von Willebrand factor
ISSN号1538-7933
DOI10.1111/jth.14822
通讯作者Jilma, Bernd(bernd.jilma@meduniwien.ac.at)
英文摘要Background BT200, a pegylated form of the aptamer BT100, inhibits binding of von Willebrand factor (VWF) to platelet glycoprotein GPIb, preventing arterial thrombosis in cynomolgus monkeys. It is being developed for secondary prevention of arterial thrombosis such as stroke or myocardial infarction. Inhibition of thrombogenesis by BT200 is expected to provide a therapeutic benefit. However, there may be unexpected bleeding (eg, incidental trauma) in which a reversal agent is required. To address this need, BT101, a complementary aptamer, has been developed to specifically inhibit BT100 and BT200 function. Objectives To characterize the effects of BT101 both in vitro and in vivo. Methods The direct interaction between BT101 and the core aptamer BT100 was evaluated using polyacrylamide gel electrophoresis. The binding of BT200 to purified human VWF and inhibition of VWF activity was further characterized using enzyme-linked immunosorbent assay. VWF-dependent platelet function was measured by the platelet function analyzer and aggregometry in whole blood. In addition, both the in vivo pharmacokinetic profile of BT101 as well as its ability to reverse BT200 activity, were evaluated in cynomolgus monkeys. Results BT101 bound to the core aptamer BT100 at a 1:1 ratio, inhibited BT200 binding to purified human VWF, and reversed BT200-induced inhibition of both VWF activity and VWF-dependent platelet function in vitro. After intravenous injection to monkeys, BT101 reversed BT200-induced effects on VWF activity and platelet function within minutes, without causing any adverse effects. Conclusions The results of this study demonstrate that BT101 is an effective reversal agent for BT200.
WOS关键词PLATELET-FUNCTION ; ISCHEMIC-STROKE ; IMPEDANCE AGGREGOMETRY ; ARTERIAL THROMBOSIS ; ASPIRIN ; CLOPIDOGREL ; MULTIPLATE ; DISEASE ; UTILITY
资助项目Guardian Therapeutics
WOS研究方向Hematology ; Cardiovascular System & Cardiology
语种英语
WOS记录号WOS:000539216400001
出版者WILEY
源URL[http://119.78.100.183/handle/2S10ELR8/291659]  
专题中国科学院上海药物研究所
通讯作者Jilma, Bernd
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai, Peoples R China
2.PMT Pharma Consulting LLC, Worcester, MA USA
3.Suzhou Ribo Life Sci Co Ltd, Kunshan City, Peoples R China
4.Guardian Therapeut Inc, Lexington, MA USA
5.Med Univ Vienna, Dept Clin Pharmacol, Waehringer Gurtel 18-20, A-1090 Vienna, Austria
推荐引用方式
GB/T 7714
Zhu, Shuhao,Gilbert, James C.,Liang, Zicai,et al. Potent and rapid reversal of the von Willebrand factor inhibitor aptamer BT200[J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS,2020:10.
APA Zhu, Shuhao.,Gilbert, James C..,Liang, Zicai.,Kang, Daiwu.,Li, Ming.,...&Jilma, Bernd.(2020).Potent and rapid reversal of the von Willebrand factor inhibitor aptamer BT200.JOURNAL OF THROMBOSIS AND HAEMOSTASIS,10.
MLA Zhu, Shuhao,et al."Potent and rapid reversal of the von Willebrand factor inhibitor aptamer BT200".JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2020):10.

入库方式: OAI收割

来源:上海药物研究所

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