Cell transplantation for Huntingtons disease: Practical and clinical considerations

Anne E. Rosser, Claire M. Kelly, Stephen B. Dunnett

Allbwn ymchwil: Cyfraniad at gyfnodolynErthygl adolyguadolygiad gan gymheiriaid

10 Dyfyniadau (Scopus)

Crynodeb

Huntingtons disease is a dominantly inherited neurodegenerative disorder, usually starting in mid-life and leading to progressive disability and early death. There are currently no disease-modifying treatments available. Cell transplantation is being considered as a potential therapy, following proof of principle that cell transplantation can improve outcomes in another basal ganglia disorder, namely Parkinsons disease. The principle aim is to replace the striatal medium spiny neurons lost in Huntingtons disease with new cells that are able to take over their function and reconnect the circuitry. This article reviews the experimental background and evidence from clinical studies that suggest that cell transplantation may improve function in Huntingtons disease, reviews the current status of the field and considers the current challenges to taking this experimental strategy forward to becoming a reliable therapeutic option.

Iaith wreiddiolSaesneg
Tudalennau (o-i)45-62
Nifer y tudalennau18
CyfnodolynFuture Neurology
Cyfrol6
Rhif cyhoeddi1
Dynodwyr Gwrthrych Digidol (DOIs)
StatwsCyhoeddwyd - 21 Rhag 2010
Cyhoeddwyd yn allanolIe

Dyfynnu hyn