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dc.contributor.authorMaxan, A
dc.contributor.authorMason, S
dc.contributor.authorSaint-Pierre, M
dc.contributor.authorSmith, E
dc.contributor.authorHo, A
dc.contributor.authorHarrower, T
dc.contributor.authorWatts, C
dc.contributor.authorTai, Y
dc.contributor.authorPavese, N
dc.contributor.authorSavage, JC
dc.contributor.authorTremblay, M-E
dc.contributor.authorGould, P
dc.contributor.authorRosser, AE
dc.contributor.authorDunnett, SB
dc.contributor.authorPiccini, P
dc.contributor.authorBarker, RA
dc.contributor.authorCicchetti, F
dc.date.accessioned2020-01-13T08:41:03Z
dc.date.issued2018-10-25
dc.description.abstractFor patients with incurable neurodegenerative disorders such as Huntington's (HD) and Parkinson's disease, cell transplantation has been explored as a potential treatment option. Here, we present the first clinicopathological study of a patient with HD in receipt of cell‐suspension striatal allografts who took part in the NEST‐UK multicenter clinical transplantation trial. Using various immunohistochemical techniques, we found a discrepancy in the survival of grafted projection neurons with respect to grafted interneurons as well as major ongoing inflammatory and immune responses to the grafted tissue with evidence of mutant huntingtin aggregates within the transplant area. Our results indicate that grafts can survive more than a decade post‐transplantation, but show compromised survival with inflammation and mutant protein being observed within the transplant site.en_GB
dc.description.sponsorshipMRCen_GB
dc.description.sponsorshipNIHRen_GB
dc.description.sponsorshipFonds de Recherche du Québec en santé (FRQS)en_GB
dc.description.sponsorshipO’Brien Foundationen_GB
dc.description.sponsorshipCanadian Institutes of Health Research (CIHR)en_GB
dc.description.sponsorshipWellcomeen_GB
dc.identifier.citationVol. 84 (6), pp. 950 - 956en_GB
dc.identifier.doi10.1002/ana.25354
dc.identifier.urihttp://hdl.handle.net/10871/40383
dc.language.isoenen_GB
dc.publisherWileyen_GB
dc.rights© 2018 The Authors. Annals of Neurology published by Wiley Periodicals, Inc. on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_GB
dc.titleOutcome of cell suspension allografts in a patient with Huntington's diseaseen_GB
dc.typeArticleen_GB
dc.date.available2020-01-13T08:41:03Z
dc.identifier.issn0364-5134
dc.descriptionThis is the final version. Available from Wiley via the DOI in this record. en_GB
dc.identifier.journalAnnals of Neurologyen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2018-09-27
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2018-09-27
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2020-01-13T08:29:11Z
refterms.versionFCDAM
refterms.dateFOA2020-01-13T08:41:10Z
refterms.panelAen_GB


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© 2018 The Authors. Annals of Neurology published by Wiley Periodicals, Inc. on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's licence is described as © 2018 The Authors. Annals of Neurology published by Wiley Periodicals, Inc. on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.