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重组人组织激肽释放酶-1用于治疗急性缺血性中风和预防复发

Recombinant Human Tissue Kallikrein-1 for Treating Acute Ischemic Stroke and Preventing Recurrence.

作者信息

Kasner Scott E, Bath Philip M, Hill Michael D, Volpi John J, Giuffre Michael, Masuoka Lorianne, Wambeke David, Madeddu Paolo R

机构信息

University of Pennsylvania School of Medicine, Division of Vascular Neurology, Philadelphia (S.E.K.).

Stroke Trials Unit, University of Nottingham, United Kingdom (P.M.B.).

出版信息

Stroke. 2025 Mar;56(3):745-753. doi: 10.1161/STROKEAHA.124.048858. Epub 2025 Jan 6.

Abstract

Novel strategies are needed for the treatment of acute ischemic stroke when revascularization therapies are not clinically appropriate or are unsuccessful. rKLK1 (recombinant human tissue kallikrein-1), a bradykinin-producing enzyme, offers a promising potential solution. In animal studies of acute stroke, there is a marked 36-fold increase in bradykinin B2 receptor on brain endothelial cells of the ischemic region. Due to this environment, rKLK1-generated bradykinin will exert a potent local vasodilation and increase brain perfusion via 3 synergistic signaling pathways downstream to the B2 receptor. Because of its preferential effect on ischemic tissue, systemic adverse effects such as hypotension are avoided with proper dosing. In addition, with initial vasodilation through recruitment of preexisting collaterals, rKLK1 promotes long-term benefit of brain perfusion by promoting new collateral formation. With an extended course of therapy for weeks after acute ischemic stroke, these multifaceted effects may also reduce the risk of stroke recurrence. A prior phase II trial demonstrated a favorable impact on clinical outcomes and recurrent strokes, particularly among patients who were not eligible for mechanical thrombectomy. A phase II/III trial has launched in this population, though opportunities for combination revascularization therapies deserve further investigation.

摘要

当血管再通治疗在临床上不合适或不成功时,需要新的策略来治疗急性缺血性中风。重组人组织激肽释放酶-1(rKLK1)是一种产生缓激肽的酶,提供了一个有前景的潜在解决方案。在急性中风的动物研究中,缺血区域脑内皮细胞上的缓激肽B2受体显著增加了36倍。由于这种环境,rKLK1产生的缓激肽将通过B2受体下游的3条协同信号通路发挥强大的局部血管舒张作用并增加脑灌注。由于其对缺血组织的优先作用,通过适当给药可避免低血压等全身不良反应。此外,通过募集预先存在的侧支血管实现初始血管舒张,rKLK1通过促进新的侧支血管形成来促进脑灌注的长期益处。在急性缺血性中风后进行数周的延长疗程治疗,这些多方面的作用也可能降低中风复发的风险。先前的一项II期试验证明对临床结局和复发性中风有有利影响,特别是在那些不符合机械取栓条件的患者中。尽管联合血管再通治疗的机会值得进一步研究,但该人群已启动了一项II/III期试验。

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