<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(6)</volume><submitter>Jin S</submitter><pubmed_abstract>Extracellular vesicles (EVs)-based cell-free therapy, particularly stem cell-derived extracellular vesicles (SC-EVs), offers new insights into treating a series of neurological disorders and becomes a promising candidate for alternative stem cell regenerative therapy. Currently, SC-EVs are considered direct therapeutic agents by themselves and/or dynamic delivery systems as they have a similar regenerative capacity of stem cells to promote neurogenesis and can easily load many functional small molecules to recipient cells in the central nervous system. Meanwhile, as non-living entities, SC-EVs avoid the uncontrollability and manufacturability limitations of live stem cell products &lt;i>in vivo&lt;/i> (&lt;i>e.g.&lt;/i>, low survival rate, immune response, and tumorigenicity) and &lt;i>in vitro&lt;/i> (&lt;i>e.g.&lt;/i>, restricted sources, complex preparation processes, poor quality control, low storage, shipping instability, and ethical controversy) by strict quality control system. Moreover, SC-EVs can be engineered or designed to enhance further overall yield, increase bioactivity, improve targeting, and extend their half-life. Here, this review provides an overview on the biological properties of SC-EVs, and the current progress in the strategies of native or bioengineered SC-EVs for nerve injury repairing is presented. Then we further summarize the challenges of recent research and perspectives for successful clinical application to advance SC-EVs from bench to bedside in neurological diseases.</pubmed_abstract><journal>Asian journal of pharmaceutical sciences</journal><pagination>779-797</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9800941</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Next generation of neurological therapeutics: Native and bioengineered extracellular vesicles derived from stem cells.</pubmed_title><pmcid>PMC9800941</pmcid><pubmed_authors>Lv Z</pubmed_authors><pubmed_authors>Shen L</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Jin S</pubmed_authors><pubmed_authors>Tan C</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Kang L</pubmed_authors><pubmed_authors>Wang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Next generation of neurological therapeutics: Native and bioengineered extracellular vesicles derived from stem cells.</name><description>Extracellular vesicles (EVs)-based cell-free therapy, particularly stem cell-derived extracellular vesicles (SC-EVs), offers new insights into treating a series of neurological disorders and becomes a promising candidate for alternative stem cell regenerative therapy. Currently, SC-EVs are considered direct therapeutic agents by themselves and/or dynamic delivery systems as they have a similar regenerative capacity of stem cells to promote neurogenesis and can easily load many functional small molecules to recipient cells in the central nervous system. Meanwhile, as non-living entities, SC-EVs avoid the uncontrollability and manufacturability limitations of live stem cell products &lt;i>in vivo&lt;/i> (&lt;i>e.g.&lt;/i>, low survival rate, immune response, and tumorigenicity) and &lt;i>in vitro&lt;/i> (&lt;i>e.g.&lt;/i>, restricted sources, complex preparation processes, poor quality control, low storage, shipping instability, and ethical controversy) by strict quality control system. Moreover, SC-EVs can be engineered or designed to enhance further overall yield, increase bioactivity, improve targeting, and extend their half-life. Here, this review provides an overview on the biological properties of SC-EVs, and the current progress in the strategies of native or bioengineered SC-EVs for nerve injury repairing is presented. Then we further summarize the challenges of recent research and perspectives for successful clinical application to advance SC-EVs from bench to bedside in neurological diseases.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-04T08:33:44.726Z</modification><creation>2025-04-04T08:33:44.726Z</creation></dates><accession>S-EPMC9800941</accession><cross_references><pubmed>36600903</pubmed><doi>10.1016/j.ajps.2022.10.002</doi></cross_references></HashMap>