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Amnion epithelial cells - a novel therapy for ischemic stroke?
Evans, Megan A; Broughton, Brad R S; Drummond, Grant R; Ma, Henry; Phan, Thanh G; Wallace, Euan M; Lim, Rebecca; Sobey, Christopher G.
Afiliación
  • Evans MA; Department of Physiology, Anatomy & Microbiology, La Trobe University, Melbourne, Australia.
  • Broughton BRS; Cardiovascular Disease Program, Department of Pharmacology, Biomedicine Discovery Institute, Monash University, Melbourne, Australia.
  • Drummond GR; Department of Physiology, Anatomy & Microbiology, La Trobe University, Melbourne, Australia.
  • Ma H; Department of Medicine, Monash University, Melbourne, Australia.
  • Phan TG; Department of Medicine, Monash University, Melbourne, Australia.
  • Wallace EM; The Ritchie Centre, Hudson Institute of Medical Research; Department of Obstetrics and Gynaecology, Monash University, Melbourne, Australia.
  • Lim R; The Ritchie Centre, Hudson Institute of Medical Research; Department of Obstetrics and Gynaecology, Monash University, Melbourne, Australia.
  • Sobey CG; Department of Physiology, Anatomy & Microbiology, La Trobe University, Melbourne, Australia.
Neural Regen Res ; 13(8): 1346-1349, 2018 Aug.
Article en En | MEDLINE | ID: mdl-30106038
ABSTRACT
Stroke is a leading cause of death and disability and new therapies are desperately needed. Given the complex nature of ischemic brain injury, it has been postulated that cell-based therapies may be useful. However, cell resources, invasive extraction procedures, immunological rejection, tumorigenesis and ethical challenges make it unlikely that many stem cell types could serve as a practical source for therapy. By contrast, these issues do not pertain to human amnion epithelial cells (hAECs), which are placenta-derived stem cells. We recently assessed the effects of systemically delivered hAECs on stroke outcome using four animal models of stroke. We demonstrated that when injected intravenously after ischemia onset, hAECs migrate preferentially to the spleen and injured brain to limit apoptosis and inflammation, and attenuate early brain infiltration of immune cells, progression of infarction and systemic immunosuppression and to ultimately ameliorate functional deficits. When administration of hAECs is delayed by 1-3 days post-stroke, long-term functional recovery can still be enhanced in young and aged mice of either sex. Moreover, our proof-of-principle findings suggest that hAECs are effective at limiting post-stroke infarct development in non-human primates. Overall, the results suggest that hAECs could be a viable clinical stroke therapy.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Neural Regen Res Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Neural Regen Res Año: 2018 Tipo del documento: Article