Extracellular Microvesicles as New Industrial Therapeutic Frontiers

被引:146
|
作者
Agrahari, Vivek [1 ]
Agrahari, Vibhuti [2 ]
Burnouf, Pierre-Alain [3 ]
Chew, Chee Ho [4 ]
Burnouf, Thierry [4 ,5 ,6 ]
机构
[1] Eastern Virginia Med Sch, CONRAD, Arlington, TX USA
[2] Shenandoah Univ, Bernard J Dunn Sch Pharm, Winchester, VA USA
[3] Acad Sinica, Inst Biomed Sci, Taipei, Taiwan
[4] Taipei Med Univ, Coll Biomed Engn, Grad Inst Biomed Mat & Tissue Engn, Taipei, Taiwan
[5] Taipei Med Univ, Coll Biomed Engn, Int PhD Program Biomed Engn, Taipei, Taiwan
[6] Taipei Med Univ, Coll Med, Int PhD Program Cell Therapy & Regenerat Med, Taipei, Taiwan
关键词
MESENCHYMAL STEM-CELLS; CLINICAL-PRACTICE GUIDELINE; STROMAL CELLS; FETAL BOVINE; IN-VITRO; VESICLES; EXOSOMES; DELIVERY; SERUM; FUNCTIONALIZATION;
D O I
10.1016/j.tibtech.2018.11.012
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Microvesicles (MVs) are subcellular physiological vehicles present in all body fluids that mediate the transfer of intercellular information within biological systems and contribute to healthy conditions. MVs have lipid bilayer membranes decorated with multiple ligands that can interact with receptors on target cells, rendering them as promising candidates for targeted delivery. The biotechnology and cell therapy industries are developing MV-based preparations that use this subcellular therapeutic machinery (in a naive or modified state) for regenerative medicine, as substitutes for intact cell therapy, and as intelligent targeted drug delivery carriers. However, significant production challenges must be overcome before MVs scale-up development, clinical translation, and routine therapeutic application can be realized. The unique expertise developed in the biotechnology industry should facilitate market access to MV-based therapeutics. In this review, the roles of biotechnology and cell therapy industries to manufacture MVs as inherent therapeutic agents or drug delivery systems are summarized. The manufacturing, development, characterization, and regulatory challenges for successful translation are discussed.
引用
收藏
页码:707 / 729
页数:23
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