短效抗vwf(血管性血友病因子)适体提高冷藏血小板的恢复、存活和止血功能

Wenchun Chen, K. Voos, C. Josephson, Renhao Li
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引用次数: 9

摘要

目的研究冷藏诱导的血管性血友病因子(VWF)与血小板的结合有助于快速清除冷藏血小板。在这项研究中,我们研究了通过基于dna的适配体抑制VWF结合是否能改善冷冻血小板的清除,而不会显著阻碍止血功能。方法和结果:用或不带适体ARC1779冷藏血小板48小时。观察VWF结合、ARC1779有效寿命、输血后血小板恢复和生存、止血功能。冷藏过程中,ARC1779处理抑制血小板- vwf相互作用。经arc1779处理的冷藏小鼠血小板在输血后的恢复和存活率均高于未处理的小鼠(经arc1779处理的血小板的恢复:76.7±5.5%;治疗:63.7±0.8%;P < 0.01。半衰期:31.4±2.36小时vs 28.1±0.86小时;P < 0.05)。冷冻的人血小板也有类似的增加(回收率:49.4±4.4% vs 36.8±2.1%,P<0.01;半衰期:9.2±1.5小时vs 8.7±0.9小时(ns)。ARC1779在小鼠体内的有效寿命为2小时。此外,ARC1779改善了冷藏血小板的长期(输注后2小时)止血功能(经ARC1779处理的冷藏血小板输注小鼠尾出血时间:160±65秒;未处理:373±96秒;P < 0.01)。输血前加入一种ARC1779解毒剂可改善立即(输血后15分钟)止血功能(治疗后血小板出血时间:149±21秒;未处理:320±36秒;P < 0.01)。结论sarc1779可改善冷藏血小板输血后的恢复,并保留冷藏血小板的长期止血功能。这些结果表明,一种短效的血小板- vwf相互作用抑制剂可能是一种潜在的治疗选择,可以改善输血治疗中血小板的冷藏。
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Short-Acting Anti-VWF (von Willebrand Factor) Aptamer Improves the Recovery, Survival, and Hemostatic Functions of Refrigerated Platelets.
OBJECTIVE Refrigeration-induced binding of VWF (von Willebrand factor) to platelets contributes to the rapid clearance of refrigerated platelets. In this study, we investigate whether inhibiting VWF binding by a DNA-based aptamer ameliorates the clearance of refrigerated platelets without significantly impeding hemostatic functions. Approach and Results: Platelets were refrigerated with or without aptamer ARC1779 for 48 hours. VWF binding, the effective lifetime of ARC1779, platelet post-transfusion recovery and survival, and the hemostatic function were measured. ARC1779 treatment during refrigeration inhibited the platelet-VWF interaction. ARC1779-treated refrigerated murine platelets exhibited increased post-transfusion recovery and survival than untreated ones (recovery of ARC1779-treated platelets: 76.7±5.5%; untreated: 63.7±0.8%; P<0.01. Half-life: 31.4±2.36 hours versus 28.1±0.86 hours; P<0.05). A similar increase was observed for refrigerated human platelets (recovery: 49.4±4.4% versus 36.8±2.1%, P<0.01; half-life: 9.2±1.5 hours versus 8.7±0.9 hours, ns). The effective lifetime of ARC1779 in mice was 2 hours. Additionally, ARC1779 improved the long-term (2 hours after transfusion) hemostatic function of refrigerated platelets (tail bleeding time of mice transfused with ARC1779-treated refrigerated platelets: 160±65 seconds; untreated: 373±96 seconds; P<0.01). The addition of an ARC1779 antidote before transfusion improved the immediate (15 minutes after transfusion) hemostatic function (bleeding time of treated platelets: 149±21 seconds; untreated: 320±36 seconds; P<0.01). CONCLUSIONS ARC1779 improves the post-transfusion recovery of refrigerated platelets and preserves the long-term hemostatic function of refrigerated platelets. These results suggest that a short-acting inhibitor of the platelet-VWF interaction may be a potential therapeutic option to improve refrigeration of platelets for transfusion treatment.
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Editors and Editorial Board. Correction to: Role of LpL (Lipoprotein Lipase) in Macrophage Polarization In Vitro and In Vivo. Tribute to Paul M. Vanhoutte, MD, PhD (1940-2019). Correction to: 18F-Sodium Fluoride Imaging of Coronary Atherosclerosis in Ambulatory Patients With Diabetes Mellitus. Extracellular MicroRNA-92a Mediates Endothelial Cell-Macrophage Communication.
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