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Chapter 14. Cell Therapy for Parkinson's Disease: Problems and Prospects

  1. Gregory Bock Organizer,
  2. Jamie Goode
  1. Anders Björklund

Published Online: 7 OCT 2008

DOI: 10.1002/0470091452.ch14

Stem Cells: Nuclear Reprogramming and Therapeutic Applications: Novartis Foundation Symposium 265

Stem Cells: Nuclear Reprogramming and Therapeutic Applications: Novartis Foundation Symposium 265

How to Cite

Björklund, A. (2008) Cell Therapy for Parkinson's Disease: Problems and Prospects, in Stem Cells: Nuclear Reprogramming and Therapeutic Applications: Novartis Foundation Symposium 265 (eds G. Bock and J. Goode), John Wiley & Sons, Ltd, Chichester, UK. doi: 10.1002/0470091452.ch14

Author Information

  1. Wallenberg Neuroscience Center, Division of Neurobiology, Lund University, BMC A11, S 22184 Lund, Sweden

Publication History

  1. Published Online: 7 OCT 2008
  2. Published Print: 18 MAR 2005

Book Series:

  1. Novartis Foundation Symposia

Book Series Editors:

  1. Novartis Foundation

ISBN Information

Print ISBN: 9780470091432

Online ISBN: 9780470091456

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Keywords:

  • Parkinson's disease (PD);
  • restorative cell therapy;
  • DA neuroblasts;
  • positron emission tomography (PET) scans;
  • multiple graft placements;
  • incomplete functional recovery;
  • DA neuron transplantation;
  • DA cell replacement;
  • nigrostriatal DA pathway degeneration

Summary

Cell replacement therapy in Parkinson's disease (PD) has so far been based on the use of primary dopaminergic (DA) neuroblasts obtained from the brain of aborted human fetuses. Clinical trials show that intrastriatal DA neuron transplants can give substantial symptomatic relief in advanced PD patients. Two recent NIH-sponsored placebo-controlled trials, however, have given disappointing results and highlighted a number of critical issues that need to be resolved in order to turn cell transplantation into an acceptable clinical therapy. First, graft survival and clinical outcome has so far been too variable, suggesting that DA neuron grafts may not be equally effective in all PD patients. Secondly, it has become clear that immune mechanisms leading to slowly developing inflammatory responses may compromise long-term graft survival and function. Third, the problems associated with the use of tissue from aborted fetuses make it necessary to develop alternative sources of cells for transplantation. Recent progress in the generation of DA neuroblasts from neural progenitors and embryonic stem cells suggest that these kinds of cell may offer more accessible, defined and standardized sources of cells for clinical transplantation in PD.