Extracellular Vesicles as a Potential Therapy for Neonatal Conditions: State of the Art and Challenges in Clinical Translation.

BPD HIE NEC ROP bronchopulmonary dysplasia exosomes hypoxic ischemic encephalopathy necrotizing enterocolitis retinopathy of prematurity spina bifida

Journal

Pharmaceutics
ISSN: 1999-4923
Titre abrégé: Pharmaceutics
Pays: Switzerland
ID NLM: 101534003

Informations de publication

Date de publication:
11 Aug 2019
Historique:
received: 30 06 2019
revised: 27 07 2019
accepted: 31 07 2019
entrez: 14 8 2019
pubmed: 14 8 2019
medline: 14 8 2019
Statut: epublish

Résumé

Despite advances in intensive care, several neonatal conditions typically due to prematurity affect vital organs and are associated with high mortality and long-term morbidities. Current treatment strategies for these babies are only partially successful or are effective only in selected patients. Regenerative medicine has been shown to be a promising option for these conditions at an experimental level, but still warrants further exploration for the development of optimal treatment. Although stem cell-based therapy has emerged as a treatment option, studies have shown that it is associated with potential risks and hazards, especially in the fragile population of babies. Recently, extracellular vesicles (EVs) have emerged as an attractive therapeutic alternative that holds great regenerative potential and is cell-free. EVs are nanosized particles endogenously produced by cells that mediate intercellular communication through the transfer of their cargo. Currently, EVs are garnering considerable attention as they are the key effectors of stem cell paracrine signaling and can epigenetically regulate target cell genes through the release of RNA species, such as microRNA. Herein, we review the emerging literature on the therapeutic potential of EVs derived from different sources for the treatment of neonatal conditions that affect the brain, retinas, spine, lungs, and intestines and discuss the challenges for the translation of EVs into clinical practice.

Identifiants

pubmed: 31405234
pii: pharmaceutics11080404
doi: 10.3390/pharmaceutics11080404
pmc: PMC6723449
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : CIHR
ID : NI18
Pays : Canada
Organisme : Sick Kids Foundation
ID : 1270R

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Auteurs

Andreea C Matei (AC)

Developmental and Stem Cell Biology Program, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.

Lina Antounians (L)

Developmental and Stem Cell Biology Program, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.

Augusto Zani (A)

Developmental and Stem Cell Biology Program, Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada. augusto.zani@sickkids.ca.
Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada. augusto.zani@sickkids.ca.

Classifications MeSH