Replacement of damaged neuronal population by fetal tissue transplantation represents a potential treatment for neurodegenerative diseases. Consistent success has been achieved with fetal striatal transplantation in Huntington's disease animal models and patients. We report the neo-generation of metabolically active tissue with striatum-like imaging features after transplantation of striatal primordia in a patient with Huntington's disease. This study represents the first "in vivo" demonstration that a human striatal anlagen, transplanted into the adult human brain, is able to progress in its development and to generate a new anatomical structure in the host, without evidence of neoplasia or teratoma.
Development of human striatal anlagen after transplantation in a patient with Huntington's disease / P. Gallina, M. Paganini, L. Lombardini, R. Saccardi, M. Marini, M.T. De Cristofaro, P. Pinzani, F. Salvianti, C. Crescioli, A. Di Rita, S. Bucciantini, C. Mechi, E. Sarchielli, M. Moretti, S. Piacentini, G. Gritti, A. Bosi, S. Sorbi, G. Orlandini, G.B. Vannelli, et al.. - In: EXPERIMENTAL NEUROLOGY. - ISSN 0014-4886. - STAMPA. - 213:(2008), pp. 241-244.
Development of human striatal anlagen after transplantation in a patient with Huntington's disease.
GALLINA, PASQUALE;MARINI, MIRCA;PINZANI, PAMELA;SARCHIELLI, ERICA;PIACENTINI, SILVIA;GRITTI, GAETANO;BOSI, ALBERTO;SORBI, SANDRO;ORLANDINI, GIOVANNI;VANNELLI, GABRIELLA;DI LORENZO, NICOLA
2008
Abstract
Replacement of damaged neuronal population by fetal tissue transplantation represents a potential treatment for neurodegenerative diseases. Consistent success has been achieved with fetal striatal transplantation in Huntington's disease animal models and patients. We report the neo-generation of metabolically active tissue with striatum-like imaging features after transplantation of striatal primordia in a patient with Huntington's disease. This study represents the first "in vivo" demonstration that a human striatal anlagen, transplanted into the adult human brain, is able to progress in its development and to generate a new anatomical structure in the host, without evidence of neoplasia or teratoma.| File | Dimensione | Formato | |
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