Department of Pharmacology, Second Military Medical University/ Naval Medical University, Shanghai, China.
Department of Pharmacology, Second Military Medical University/ Naval Medical University, Shanghai, China
Stroke Vasc Neurol. 2024 Nov 5;9(5):467-480. doi: 10.1136/svn-2023-002883.
The use of biologics in various diseases has dramatically increased in recent years. Stroke, a cerebrovascular disease, is the second most common cause of death, and the leading cause of disability with high morbidity worldwide. For biologics applied in the treatment of acute ischaemic stroke, alteplase is the only thrombolytic agent. Meanwhile, current clinical trials show that two recombinant proteins, tenecteplase and non-immunogenic staphylokinase, are most promising as new thrombolytic agents for acute ischaemic stroke therapy. In addition, stem cell-based therapy, which uses stem cells or organoids for stroke treatment, has shown promising results in preclinical and early clinical studies. These strategies for acute ischaemic stroke mainly rely on the unique properties of undifferentiated cells to facilitate tissue repair and regeneration. However, there is a still considerable journey ahead before these approaches become routine clinical use. This includes optimising cell delivery methods, determining the ideal cell type and dosage, and addressing long-term safety concerns. This review introduces the current or promising recombinant proteins for thrombolysis therapy in ischaemic stroke and highlights the promise and challenges of stem cells and cerebral organoids in stroke therapy.
近年来,生物制剂在各种疾病中的应用显著增加。中风是一种脑血管疾病,是全球第二大致死原因,也是致残的主要原因,发病率高。对于应用于急性缺血性中风治疗的生物制剂,阿替普酶是唯一的溶栓剂。同时,目前的临床试验表明,两种重组蛋白,替奈普酶和非免疫性葡萄球菌激酶,作为急性缺血性中风治疗的新型溶栓剂最有前途。此外,基于干细胞的疗法,使用干细胞或类器官治疗中风,在临床前和早期临床试验中显示出有希望的结果。这些急性缺血性中风的治疗策略主要依赖于未分化细胞的独特特性,以促进组织修复和再生。然而,在这些方法成为常规临床应用之前,还有相当长的路要走。这包括优化细胞输送方法、确定理想的细胞类型和剂量,以及解决长期安全性问题。本综述介绍了目前或有前途的用于缺血性中风溶栓治疗的重组蛋白,并强调了干细胞和脑类器官在中风治疗中的前景和挑战。