Please use this identifier to cite or link to this item: https://doi.org/10.3389/fphar.2014.00223
DC FieldValue
dc.titlePrenatal transplantation of mesenchymal stem cells to treat osteogenesis imperfecta
dc.contributor.authorChan, J.K.Y
dc.contributor.authorGötherström, C
dc.date.accessioned2020-10-27T11:12:24Z
dc.date.available2020-10-27T11:12:24Z
dc.date.issued2014
dc.identifier.citationChan, J.K.Y, Götherström, C (2014). Prenatal transplantation of mesenchymal stem cells to treat osteogenesis imperfecta. Frontiers in Pharmacology 5 (OCT) : 223. ScholarBank@NUS Repository. https://doi.org/10.3389/fphar.2014.00223
dc.identifier.issn16639812
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181526
dc.description.abstractOsteogenesis imperfecta (OI) can be a severe disorder that can be diagnosed before birth. Transplantation of mesenchymal stem cells (MSC) has the potential to improve the bone structure, growth, and fracture healing. In this review, we give an introduction to OI and MSC, and the basis for pre- and postnatal transplantation in OI. We also summarize the two patients with OI who have received pre- and postnatal transplantation of MSC. The findings suggest that prenatal transplantation of allogeneic MSC in OI is safe. The cell therapy is of likely clinical benefit with improved linear growth, mobility, and reduced fracture incidence. Unfortunately, the effect is transient. For this reason, postnatal booster infusions using same-donor MSC have been performed with clinical benefit, and without any adverse events. So far there is limited experience in this specific field and proper studies are required to accurately conclude on clinical benefits of MSC transplantation to treat OI. © 2014 Chan and Götherström.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectbisphosphonic acid derivative
dc.subjectallogeneic stem cell transplantation
dc.subjectallogenic bone marrow transplantation
dc.subjectalloimmunity
dc.subjectautosomal dominant inheritance
dc.subjectbone dysplasia
dc.subjectclinical effectiveness
dc.subjectcompression fracture
dc.subjectengraftment
dc.subjectfeasibility study
dc.subjectfemur fracture
dc.subjectfetal stem cell
dc.subjecthuman
dc.subjectimmunomodulation
dc.subjectmesenchymal stem cell
dc.subjectnonhuman
dc.subjectosteoblast
dc.subjectosteogenesis imperfecta
dc.subjectpostnatal care
dc.subjectprenatal care
dc.subjectprenatal transplantation
dc.subjectShort Survey
dc.typeOthers
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.3389/fphar.2014.00223
dc.description.sourcetitleFrontiers in Pharmacology
dc.description.volume5
dc.description.issueOCT
dc.description.page223
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