首页> 外文期刊>Frontiers in Bioengineering and Biotechnology >Mesenchymal Stem Cell-Derived Extracellular Vesicles: Opportunities and Challenges for Clinical Translation
【24h】

Mesenchymal Stem Cell-Derived Extracellular Vesicles: Opportunities and Challenges for Clinical Translation

机译:间充质干细胞衍生的细胞外囊泡:临床翻译的机会和挑战

获取原文
           

摘要

Extracellular vesicles (EVs), including exosomes and microvesicles, derived from mesenchymal stem/stromal cells (MSCs) exert similar effects as their parental cells, and are of interest for various therapeutic applications. EVs can act through uptake by the target cells followed by release of their cargo inside the cytoplasm, or through interaction of membrane-bound ligands with receptors expressed on target cells to stimulate downstream intracellular pathways. EV-based therapeutics may be directly used as substitutes of intact cells or after modification for targeted drug delivery. However, for the development of EV-based therapeutics, several production, isolation, and characterization requirements have to be met and the quality control of the final product have to be tested before its clinical implementation. In this review, we discuss the challenges associated with the development of EV-based therapeutics and the regulatory specifications for their successful clinical translation.
机译:细胞外囊(EV),包括从间充质茎/基质细胞(MSCs)衍生的外泌体和微泡(MSCs)作为其亲本细胞的效果,对各种治疗应用感兴趣。 EVS可以通过靶细胞的吸收作用,然后通过释放其在细胞质内的货物,或者通过膜结合配体与靶细胞上表达的受体的相互作用来释放,以刺激下游的细胞内途径。基于EV的治疗剂可以直接用作完整细胞的替代物或用于靶向药物递送的修饰后。然而,对于基于EV的治疗方法的发展,必须满足几种生产,隔离和表征要求,并且必须在其临床实施之前进行最终产品的质量控制。在这篇综述中,我们讨论了与EV的治疗方法的发展有关的挑战,以及其成功临床翻译的监管规范。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号