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Updated: Apr 24, 2026

Isolation and Characterization of Human Umbilical Cord-derived Mesenchymal Stem Cells from Preterm and Term Infants
Published on: January 26, 2019
Hematopoietic stem cells in neonates: any differences between very preterm and term neonates?
Lukas Wisgrill1, Simone Schüller1, Markus Bammer1
1Dept. of Pediatrics and Adolescent Medicine, Division of Neonatology, Paediatric Intensive Care & Neuropaediatrics, Medical University of Vienna, Vienna, Austria.
Preterm cord blood has more hematopoietic stem and progenitor cells (HSPCs) with greater growth potential than term cord blood. This finding suggests potential for HSPCs in treating preterm infants.
Area of Science:
- Hematology
- Neonatology
- Regenerative Medicine
Background:
- Human full-term cord blood is a known source of hematopoietic stem and progenitor cells (HSPCs).
- Limited understanding exists regarding HSPC function in preterm neonates, despite interest in regenerative therapies.
Purpose of the Study:
- To investigate HSPC concentration and clonogenic capacity in preterm versus term cord blood.
- To determine the influence of perinatal factors on HSPC subsets.
Main Methods:
- Flow cytometry analyzed CD34+ HSPC subsets in 30 preterm and 30 term cord blood samples.
- Clonogenic assays assessed the proliferative potential of HSPCs, including subsets defined by CD133 and ALDH activity.
Main Results:
- Preterm cord blood showed significantly higher concentrations of CD34+ HSPCs and enhanced clonogenic capacity.
- Maternal age, gestational age, and white blood cell count influenced HSPC counts; gestational age impacted clonogenic potential.
- Isolated preterm HSPC subsets (CD34+/CD133+, CD34+/CD133-, ALDH(high)) exhibited greater clonogenic potential than term counterparts.
Conclusions:
- Preterm cord blood demonstrates superior HSPC concentration and clonogenic capacity compared to term cord blood.
- These findings support the potential use of HSPCs in autologous stem cell therapy for preterm neonates.
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