» Articles » PMID: 37623531

Progress in Research on Stem Cells in Neonatal Refractory Diseases

Overview
Journal J Pers Med
Date 2023 Aug 25
PMID 37623531
Authors
Affiliations
Soon will be listed here.
Abstract

With the development and progress of medical technology, the survival rate of premature and low-birth-weight infants has increased, as has the incidence of a variety of neonatal diseases, such as hypoxic-ischemic encephalopathy, intraventricular hemorrhage, bronchopulmonary dysplasia, necrotizing enterocolitis, and retinopathy of prematurity. These diseases cause severe health conditions with poor prognoses, and existing control methods are ineffective for such diseases. Stem cells are a special type of cells with self-renewal and differentiation potential, and their mechanisms mainly include anti-inflammatory and anti-apoptotic properties, reducing oxidative stress, and boosting regeneration. Their paracrine effects can affect the microenvironment in which they survive, thereby affecting the biological characteristics of other cells. Due to their unique abilities, stem cells have been used in treating various diseases. Therefore, stem cell therapy may open up the possibility of treating such neonatal diseases. This review summarizes the research progress on stem cells and exosomes derived from stem cells in neonatal refractory diseases to provide new insights for most researchers and clinicians regarding future treatments. In addition, the current challenges and perspectives in stem cell therapy are discussed.

Citing Articles

Therapeutic role of extracellular vesicles from human umbilical cord mesenchymal stem cells and their wide therapeutic implications in inflammatory bowel disease and other inflammatory disorder.

Azhar Ud Din M, Wan A, Chu Y, Zhou J, Yan Y, Xu Z Front Med (Lausanne). 2024; 11:1406547.

PMID: 39139783 PMC: 11319305. DOI: 10.3389/fmed.2024.1406547.

References
1.
Murphy S, Atala A . Amniotic fluid and placental membranes: unexpected sources of highly multipotent cells. Semin Reprod Med. 2013; 31(1):62-8. DOI: 10.1055/s-0032-1331799. View

2.
Bottai D, Cigognini D, Nicora E, Moro M, Grimoldi M, Adami R . Third trimester amniotic fluid cells with the capacity to develop neural phenotypes and with heterogeneity among sub-populations. Restor Neurol Neurosci. 2012; 30(1):55-68. DOI: 10.3233/RNN-2011-0620. View

3.
Nabetani M, Shintaku H, Hamazaki T . Future perspectives of cell therapy for neonatal hypoxic-ischemic encephalopathy. Pediatr Res. 2017; 83(1-2):356-363. DOI: 10.1038/pr.2017.260. View

4.
Ohshima M, Taguchi A, Sato Y, Ogawa Y, Saito S, Yamahara K . Evaluations of Intravenous Administration of CD34+ Human Umbilical Cord Blood Cells in a Mouse Model of Neonatal Hypoxic-Ischemic Encephalopathy. Dev Neurosci. 2017; 38(5):331-341. DOI: 10.1159/000454830. View

5.
Fisher S, Cutler A, Doree C, Brunskill S, Stanworth S, Navarrete C . Mesenchymal stromal cells as treatment or prophylaxis for acute or chronic graft-versus-host disease in haematopoietic stem cell transplant (HSCT) recipients with a haematological condition. Cochrane Database Syst Rev. 2019; 1:CD009768. PMC: 6353308. DOI: 10.1002/14651858.CD009768.pub2. View