TY - JOUR
T1 - Past and future of neurotrophic growth factors therapies in ALS
T2 - From single neurotrophic growth factor to stem cells and human platelet lysates
AU - Gouel, Flore
AU - Rolland, Anne Sophie
AU - Devedjian, Jean Christophe
AU - Burnouf, Thierry
AU - Devos, David
N1 - Funding Information:
The authors wish to acknowledge support from the ARSLA charity (Association pour la Recherche sur la Sclérose Latérale Amyotrophique et autres maladies du motoneurone), ISITE- ULNE Foundation, Credit Agricole Foundation, and SATT NORD.
Funding Information:
The authors wish to acknowledge support from the ARSLA charity (Association pour la Recherche sur la Sclérose Latérale Amyotrophique et autres maladies du motoneurone), I-SITE-ULNE Foundation, Credit Agricole Foundation, and SATT NORD.
Publisher Copyright:
Copyright © 2019 Gouel, Rolland, Devedjian, Burnouf and Devos.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - 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.
AB - 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.
KW - Amyotrophic lateral sclerosis
KW - Growth factors
KW - Human platelet lysate
KW - Stem cell
KW - Therapeutic
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U2 - 10.3389/fneur.2019.00835
DO - 10.3389/fneur.2019.00835
M3 - Article
AN - SCOPUS:85070792035
SN - 1664-2295
VL - 10
JO - Frontiers in Neurology
JF - Frontiers in Neurology
IS - JUL
M1 - 835
ER -