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Advances in stem cell therapy for amyotrophic lateral sclerosis

Authors :
Mazzini, L
Ferrari, D
Andjus, P
Buzanska, L
Cantello, R
De Marchi, F
Gelati, M
Giniatullin, R
Glover, J
Grilli, M
Kozlova, E
Maioli, M
Mitrečić, D
Pivoriunas, A
Sanchez-Pernaute, R
Sarnowska, A
Vescovi, A
Mazzini, Letizia
Ferrari, Daniela
Andjus, Pavle R
Buzanska, Leonora
Cantello, Roberto
De Marchi, Fabiola
Gelati, Maurizio
Giniatullin, Rashid
Glover, Joel C.
Grilli, Mariagrazia
Kozlova, Elena N.
Maioli, Margherita
Mitrečić, Dinko
Pivoriunas, Augustas
Sanchez-Pernaute, Rosario
Sarnowska, Anna
Vescovi, Angelo L.
Mazzini, L
Ferrari, D
Andjus, P
Buzanska, L
Cantello, R
De Marchi, F
Gelati, M
Giniatullin, R
Glover, J
Grilli, M
Kozlova, E
Maioli, M
Mitrečić, D
Pivoriunas, A
Sanchez-Pernaute, R
Sarnowska, A
Vescovi, A
Mazzini, Letizia
Ferrari, Daniela
Andjus, Pavle R
Buzanska, Leonora
Cantello, Roberto
De Marchi, Fabiola
Gelati, Maurizio
Giniatullin, Rashid
Glover, Joel C.
Grilli, Mariagrazia
Kozlova, Elena N.
Maioli, Margherita
Mitrečić, Dinko
Pivoriunas, Augustas
Sanchez-Pernaute, Rosario
Sarnowska, Anna
Vescovi, Angelo L.
Publication Year :
2018

Abstract

Introduction: Amyotrophic Lateral Sclerosis (ALS) is a progressive, incurable neurodegenerative disease that targets motoneurons. Cell-based therapies have generated widespread interest as a potential therapeutic approach but no conclusive results have yet been reported either from pre-clinical or clinical studies. Areas covered: This is an integrated review of pre-clinical and clinical studies focused on the development of cell-based therapies for ALS. We analyze the biology of stem cell treatments and results obtained from pre-clinical models of ALS and examine the methods and the results obtained to date from clinical trials. We discuss scientific, clinical, and ethical issues and propose some directions for future studies. Expert opinion: While data from individual studies are encouraging, stem-cell-based therapies do not yet represent a satisfactory, reliable clinical option. The field will critically benefit from the introduction of well-designed, randomized and reproducible, powered clinical trials. Comparative studies addressing key issues such as the nature, properties, and number of donor cells, the delivery mode and the selection of proper patient populations that may benefit the most from cell-based therapies are now of the essence. Multidisciplinary networks of experts should be established to empower effective translation of research into the clinic.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1308927423
Document Type :
Electronic Resource