Cell therapy for neonatal hypoxia-ischemia and cerebral palsy

被引:135
作者
Bennet, Laura [1 ]
Tan, Sidhartha [2 ]
Van den Heuij, Lotte [1 ]
Derrick, Matthew [2 ]
Groenendaal, Floris [3 ]
van Bel, Frank [3 ]
Juul, Sandra [4 ]
Back, Stephen A. [5 ]
Northington, Frances [6 ,7 ]
Robertson, Nicola J. [8 ]
Mallard, Carina [9 ]
Gunn, Alistair Jan [1 ,10 ]
机构
[1] Univ Auckland, Dept Physiol, Auckland 1, New Zealand
[2] NorthShore Univ HealthSyst, Dept Pediat, Evanston, IL USA
[3] Univ Med Ctr Utrecht, Dept Neonatol, Utrecht, Netherlands
[4] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[5] Oregon Hlth & Sci Univ, Dept Pediat, Portland, OR 97201 USA
[6] Johns Hopkins Sch Med, Div Neonatol, Baltimore, MD USA
[7] Johns Hopkins Sch Med, Neonatal Res Lab, Baltimore, MD USA
[8] UCL, Inst Womens Hlth, London, England
[9] Univ Gothenburg, Sahlgrenska Acad, Dept Physiol, Inst Neurosci & Physiol, Gothenburg, Sweden
[10] Univ Auckland, Dept Paediat, Auckland, New Zealand
关键词
NEURAL STEM-CELLS; CORD BLOOD-CELLS; ADULT PROGENITOR CELLS; BRAIN-INJURY; BEHAVIORAL RECOVERY; TRANSPLANTATION; RATS; DAMAGE; GRAFTS; MOUSE;
D O I
10.1002/ana.22670
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Perinatal hypoxicischemic brain injury remains a major cause of cerebral palsy. Although therapeutic hypothermia is now established to improve recovery from hypoxiaischemia (HI) at term, many infants continue to survive with disability, and hypothermia has not yet been tested in preterm infants. There is increasing evidence from in vitro and in vivo preclinical studies that stem/progenitor cells may have multiple beneficial effects on outcome after hypoxicischemic injury. Stem/progenitor cells have shown great promise in animal studies in decreasing neurological impairment; however, the mechanisms of action of stem cells, and the optimal type, dose, and method of administration remain surprisingly unclear, and some studies have found no benefit. Although cell-based interventions after completion of the majority of secondary cell death appear to have potential to improve functional outcome for neonates after HI, further rigorous testing in translational animal models is required before randomized controlled trials should be considered. ANN NEUROL 2012;
引用
收藏
页码:589 / 600
页数:12
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