학술논문

Preclinical translation of exosomes derived from mesenchymal stem/stromal cells
Document Type
article
Source
Stem Cells. 38(1)
Subject
Medical Biotechnology
Biomedical and Clinical Sciences
Biotechnology
Stem Cell Research - Nonembryonic - Non-Human
Stem Cell Research
Regenerative Medicine
Stem Cell Research - Nonembryonic - Human
5.2 Cellular and gene therapies
Development of treatments and therapeutic interventions
Generic health relevance
Cells
Cultured
Exosomes
Humans
Mesenchymal Stem Cells
exosomes
extracellular vesicles
mesenchymal stem cells
mesenchymal stromal cells
microvesicles
Biological Sciences
Technology
Medical and Health Sciences
Immunology
Biological sciences
Biomedical and clinical sciences
Language
Abstract
Exosomes are nanovesicles secreted by virtually all cells. Exosomes mediate the horizontal transfer of various macromolecules previously believed to be cell-autonomous in nature, including nonsecretory proteins, various classes of RNA, metabolites, and lipid membrane-associated factors. Exosomes derived from mesenchymal stem/stromal cells (MSCs) appear to be particularly beneficial for enhancing recovery in various models of disease. To date, there have been more than 200 preclinical studies of exosome-based therapies in a number of different animal models. Despite a growing number of studies reporting the therapeutic properties of MSC-derived exosomes, their underlying mechanism of action, pharmacokinetics, and scalable manufacturing remain largely outstanding questions. Here, we review the global trends associated with preclinical development of MSC-derived exosome-based therapies, including immunogenicity, source of exosomes, isolation methods, biodistribution, and disease categories tested to date. Although the in vivo data assessing the therapeutic properties of MSC-exosomes published to date are promising, several outstanding questions remain to be answered that warrant further preclinical investigation.