Cord blood-derived cell therapies for preterm brain injury

Abdul Razak1, Lindsay Zhou1, Graham Jenkin2

  • 1Department of Paediatrics, Monash University, Melbourne, Australia; Monash Newborn, Monash Children's Hospital, Melbourne, Australia; The Ritchie Centre, Hudson Institute of Medical Research, Melbourne, Australia.

Early Human Development
|August 29, 2025
PubMed

Insights

Umbilical cord blood cell therapy shows promise for treating preterm brain injuries by reducing inflammation and improving outcomes. Early clinical trials focus on safety and feasibility, with larger efficacy studies now underway.

Area of Science:

  • Neonatal Neurology
  • Regenerative Medicine
  • Neuroscience

Background:

  • Preterm birth (before 37 weeks) causes significant neonatal morbidity and long-term neurodevelopmental issues.
  • Brain injuries like intraventricular hemorrhage and hypoxic-ischemic encephalopathy are common in preterm infants, with limited treatment options.
  • These injuries share pathological mechanisms including inflammation, cerebrovascular immaturity, and impaired repair.

Purpose of the Study:

  • To explore the potential of umbilical cord blood (UCB)-derived cell therapy as a novel treatment for preterm brain injuries.
  • To review preclinical and early clinical evidence for UCB-derived cell therapy targeting shared pathophysiological pathways in preterm brain injury.
  • To identify current research gaps and future directions for clinical translation of UCB therapies.

Main Methods:

  • Review of preclinical studies in rodent and large-animal models investigating UCB-derived cell therapy effects.
  • Analysis of early-stage clinical trials assessing the safety and feasibility of UCB-derived cell therapies in preterm infants.
  • Examination of case series and ongoing trials for specific preterm brain injury types.

Main Results:

  • Preclinical models demonstrate UCB therapy attenuates neuroinflammation, reduces apoptosis, promotes oligodendrocyte maturation, and improves functional outcomes.
  • Early clinical research indicates UCB-derived cell therapy is feasible and safe, with some case series suggesting benefits for intraventricular hemorrhage.
  • Recent studies using autologous UCB cells show promise in reducing cerebral palsy risk, with larger efficacy trials now in progress.

Conclusions:

  • UCB-derived cell therapy offers a promising regenerative strategy for preterm brain injuries by addressing multiple pathophysiological mechanisms.
  • While preclinical data are consistent, clinical translation requires larger efficacy trials, particularly for severe or established injuries.
  • Ongoing and future trials are crucial for establishing the therapeutic efficacy of UCB-derived cells in diverse preterm brain injury contexts.