| Literature DB >> 18335482 |
Neil Cashman1, Lih-Yeen Tan, Charles Krieger, Burkhard Mädler, Alex Mackay, Ian Mackenzie, Barrett Benny, Stephen Nantel, Marife Fabros, Leslie Shinobu, Masoud Yousefi, Andrew Eisen.
Abstract
Amyotrophic lateral sclerosis (ALS) is characterized by degeneration of upper and lower motor neurons in the brain, brainstem, and spinal cord. It has been proposed that bone marrow (BM)-derived cells might supply motor neurons and other cells with a cellular milieu more conducive to survival in ALS. Direct injection of stem cells in ALS is problematic because of the large expanse of the neuraxis that would need to be injected. We reasoned that transiently increasing the number of circulating hematopoietic stem cells might be a useful therapeutic approach. However, agents stimulating the activation and mobilization of hematopoietic stem cells may have adverse effects such as activation of microglial cells. We conducted a small pilot trial of the collection and reinfusion of granulocyte-colony stimulating factor (G-CSF)-mobilized peripheral blood stem cells (PBSC) in ALS patients and found no adverse effects, paving the way for a properly powered therapeutic trial with an optimized regimen of G-CSF.Entities:
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Year: 2008 PMID: 18335482 DOI: 10.1002/mus.20951
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217