AI Article Synopsis

  • The COVID-19 pandemic, caused by a new coronavirus, led to a reevaluation of treatments using mesenchymal stem cells (MSCs) and their extracellular vesicles (specifically exosomes).
  • MSCs initially showed promise in early treatments, but safety concerns related to their use prompted increased focus on exosomes, which exhibit similar therapeutic effects without the same risks.
  • The review aims to explore the potential of MSC-derived exosomes in treating COVID-19 and compares the challenges and advancements in using these exosomes versus their original stem cells.

Article Abstract

It only took 8 months for the pneumonia caused by a previously unknown coronavirus to turn into a global pandemic of unprecedentedly far-reaching implications. Failure of the already discovered treatment measures opened up a new opportunity to evaluate the potentials of mesenchymal stem cells and their extracellular vesicles (EVs), exosomes in particular. Eventually, the initial success experienced after the use of MSCs in treating the new pneumonia by Lnge and his team backed up the idea of MSC-based therapies and pushed them closer to becoming a reality. However, MSC-related concerns regarding safety such as abnormal differentiation, spontaneous malignant and the formation of ectopic tissues have triggered the replacement of MSCs by their secreted exosomes. The issue has been further strengthened by the fact that the exosomes leave similar treatment impacts when compared to their parental cells. In recent years, much attention has been paid to the use of MSC-derived exosomes in the treatment of a variety of diseases. With a primary focus on COVID-19 and its current treatment methods, the present review looks into the potentials of MSCs and MSC-derived exosomes in battling the ongoing pandemic. Finally, the research will draw an analogy between exosomes and their parental cells, when it comes to the progresses and challenges in using exosomes as a large-scale treatment method.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8765836PMC
http://dx.doi.org/10.1007/s10529-021-03209-8DOI Listing

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