Neural transplants in patients with Huntington's disease undergo disease-like neuronal degeneration

F. Cicchetti, S. Saporta, R. A. Hauser, M. Parent, M. Saint-Pierre, P. R. Sanberg, X. J. Li, J. R. Parker, Y. Chu, E. J. Mufson, J. H. Kordower, T. B. Freeman

Research output: Contribution to journalArticlepeer-review

157 Scopus citations

Abstract

The clinical evaluation of neural transplantation as a potential treatment for Huntington's disease (HD) was initiated in an attempt to replace lost neurons and improve patient outcomes. Two of 3 patients with HD reported here, who underwent neural transplantation containing striatal anlagen in the striatum a decade earlier, have demonstrated marginal and transient clinical benefits. Their brains were evaluated immunohistochemically and with electron microscopy for markers of projection neurons and interneurons, inflammatory cells, abnormal huntingtin protein, and host-derived connectivity. Surviving grafts were identified bilaterally in 2 of the subjects and displayed classic striatal projection neurons and interneurons. Genetic markers of HD were not expressed within the graft. Here we report in patients with HD that (i) graft survival is attenuated long-term; (ii) grafts undergo disease-like neuronal degeneration with a preferential loss of projection neurons in comparison to interneurons; (iii) immunologically unrelated cells degenerate more rapidly than the patient's neurons, particularly the projection neuron subtype; (iv) graft survival is attenuated in the caudate in comparison to the putamen in HD; (v) glutamatergic cortical neurons project to transplanted striatal neurons; and (vi) microglial inflammatory changes in the grafts specifically target the neuronal components of the grafts. These results, when combined, raise uncertainty about this potential therapeutic approach for the treatment of HD. However, these observations provide new opportunities to investigate the underlying mechanisms involved in HD, as well as to explore additional therapeutic paradigms.

Original languageEnglish (US)
Pages (from-to)12483-12488
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume106
Issue number30
DOIs
StatePublished - Jul 28 2009
Externally publishedYes

Keywords

  • Excitotoxicity
  • Glutamate
  • Inflammation
  • Microglia
  • Mutant huntingtin

ASJC Scopus subject areas

  • General

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