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载外泌体的可降解聚合物微胶囊用于治疗玻璃体视网膜疾病。

Exosome-loaded degradable polymeric microcapsules for the treatment of vitreoretinal diseases.

机构信息

State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, P. R. China.

Department of Ophthalmology, Beijing Chaoyang Hospital, Capital Medical University, Beijing, P. R. China.

出版信息

Nat Biomed Eng. 2024 Nov;8(11):1436-1452. doi: 10.1038/s41551-023-01112-3. Epub 2023 Oct 23.

Abstract

The therapeutic benefits of many cell types involve paracrine mechanisms. Inspired by the paracrine functions of exosomes and the sustained degradation properties of microcapsules, here we report the therapeutic benefits of exosome-loaded degradable poly(lactic-co-glycolic acid) microcapsules with micrometric pores for the treatment of vitreoretinal diseases. On intravitreal injection in a mouse model of retinal ischaemia-reperfusion injury, microcapsules encapsulating mouse mesenchymal-stem-cell-derived exosomes settled in the inferior vitreous cavity, released exosomes for over one month as they underwent degradation and led to the restoration of retinal thickness to nearly that of the healthy retina. In mice and non-human primates with primed mycobacterial uveitis, intravitreally injected microcapsules loaded with exosomes from monkey regulatory T cells resulted in a substantial reduction in the levels of inflammatory cells. The exosome-encapsulating microcapsules, which can be lyophilised, may offer alternative treatment options for vitreoretinal diseases.

摘要

许多细胞类型的治疗益处涉及旁分泌机制。受外泌体旁分泌功能和微胶囊持续降解特性的启发,我们在此报告了负载有外泌体的可降解聚(乳酸-共-乙醇酸)微胶囊的治疗益处,这些微胶囊具有微米级孔,可用于治疗玻璃体视网膜疾病。在视网膜缺血再灌注损伤的小鼠模型中,通过玻璃体内注射,包载有鼠间充质干细胞衍生的外泌体的微胶囊在玻璃体腔中沉淀,随着微胶囊的降解,外泌体持续释放超过一个月,从而使视网膜厚度恢复到接近健康视网膜的水平。在经预先致敏的分枝杆菌性葡萄膜炎的小鼠和非人灵长类动物中,玻璃体内注射负载有猴调节性 T 细胞外泌体的微胶囊可显著降低炎症细胞的水平。可冻干的负载外泌体的微胶囊可能为玻璃体视网膜疾病提供了替代的治疗选择。

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