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2000
Volume 5, Issue 4
  • ISSN: 1574-888X
  • E-ISSN: 2212-3946

Abstract

Cellular therapies represent a new frontier in the treatment of neurological disease. Mesenchymal stem cells (MSCs), which can be harvested from bone marrow, adipose tissue, and umbilical cord blood, among many other sources, possess several qualities which may be used to treat diseases of the central nervous system. MSCs migrate to sites of malignancy, a property which may be used for the treatment of brain cancer. MSCs possess immunosuppressive properties, which may be used for the treatment of neurological disorders with an inflammatory etiology. Finally, MSCs restore injured neural tissue, a property which may be used for the treatment of neural injury. Approximately 23 clinical trials have been completed to date, with many more ongoing, and all have been listed in this review. The long-term safety of MSC-based therapies is not well established, and continues to be one major limitation to clinical translation. More broadly, only a small minority of clinical trials have employed rigorous designs that include prospective randomization, patients from multiple centers, clinically-relevant and reproducible endpoints, and adequate long-term follow-up. These limitations must be addressed before MSCs can enter widespread clinical use. Nevertheless, MSCs represent a promising new approach to treating diseases of the central nervous system that are traditionally associated with morbid outcomes. With additional pre-clinical and clinical studies that focus on their potential benefits as well as dangers, MSCs may one day find translation to clinical use in the setting of neurological disease.

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/content/journals/cscr/10.2174/157488810793351631
2010-12-01
2025-09-18
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  • Article Type:
    Research Article
Keyword(s): adhesion molecules; adipogenic; adipose tissue; allogeneic donors; Alzheimer disease; amyloid formation; Amyotrophic Lateral Sclerosis; angiogenesis; B Lymphocytes; basal forbrain; biosafety; brain cancer; brain neoplasms; cell transplantation; central nervous system; chemotactic potential; chondrocytes; chromosomal anomalies; clinical applications; clinical trial; colony-forming unit fibroblasts; cytotoxic effect; defensive mechanisms; Dendritic Cells; excitioxocity; fibroblasts; forebrain cholinergic neurons; gastrointestinal inflammation; glands; graft-versus-host disease; HARVESTING MESENCHYMAL STEM CELLS; Helicobacter pylori; implantation of Renca adenocarcinoma; inflammatory component; insertional mutagenesis; interferon; ipsilateral carotid artery; isoform of the human leukocyte; Lewis lung carcinoma; ligands; liposuction; marrow stromal cells; maternal tolerance; melanoma lung metastasis models; Mesenchymal stem cells; metastasis; migration toward cancer; mononuclear cells; morbidity; mortality; multiple cell types; myocardial infarction; Natural Killer Cells; nervous system diseases; NEURODEGENERATIVE DISORDERS; neurosurgical procedures; Neutrophils; nological cells; non-adherent cells; non-ischemic hemisphere; osteoblasts; osteocytic, chondrocytic; Parkinson disease; pathogenic material; periodontal ligament; placenta; Plastic-adherence; postmortem brain; proliferation; restoration of injured tissue; stroke; T Lymphocytes; T-regulatory cells; TREATMENT OF ISCHEMIC NEURAL INJURY; Treatment of Neurological Diseases; Treatment of Stroke; Tumor Growth; umbilical cord blood
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