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Past and Future of Neurotrophic Growth Factors Therapies in ALS: From Single Neurotrophic Growth Factor to Stem Cells and Human Platelet Lysates

Overview
Journal Front Neurol
Specialty Neurology
Date 2019 Aug 21
PMID 31428042
Citations 21
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Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that typically results in death within 3-5 years after diagnosis. To date, there is no curative treatment and therefore an urgent unmet need of neuroprotective and/or neurorestorative treatments. Due to their spectrum of capacities in the central nervous system-e.g., development, plasticity, maintenance, neurogenesis-neurotrophic growth factors (NTF) have been exploited for therapeutic strategies in ALS for decades. In this review we present the initial strategy of using single NTF by different routes of administration to the use of stem cells transplantation to express a multiple NTFs-rich secretome to finally focus on a new biotherapy based on the human platelet lysates, the natural healing system containing a mix of pleitropic NTF and having immunomodulatory function. This review highlights that this latter treatment may be crucial to power the neuroprotection and/or neurorestoration therapy requested in this devastating disease.

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References
1.
Boonman Z, Isacson O . Apoptosis in neuronal development and transplantation: role of caspases and trophic factors. Exp Neurol. 1999; 156(1):1-15. DOI: 10.1006/exnr.1999.7056. View

2.
. A controlled trial of recombinant methionyl human BDNF in ALS: The BDNF Study Group (Phase III). Neurology. 1999; 52(7):1427-33. DOI: 10.1212/wnl.52.7.1427. View

3.
Ende N, Weinstein F, Chen R, Ende M . Human umbilical cord blood effect on sod mice (amyotrophic lateral sclerosis). Life Sci. 2000; 67(1):53-9. DOI: 10.1016/s0024-3205(00)00602-0. View

4.
Chen R, Ende N . The potential for the use of mononuclear cells from human umbilical cord blood in the treatment of amyotrophic lateral sclerosis in SOD1 mice. J Med. 2000; 31(1-2):21-30. View

5.
Ochs G, Penn R, York M, Giess R, Beck M, Tonn J . A phase I/II trial of recombinant methionyl human brain derived neurotrophic factor administered by intrathecal infusion to patients with amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001; 1(3):201-6. DOI: 10.1080/14660820050515197. View