Antibody-Based Therapeutic Interventions for Amyotrophic Lateral Sclerosis: A Systematic Literature Review

Amyotrophic Lateral Sclerosis (ALS) is a mid-life onset neurodegenerative disease that manifests its symptomatology with motor impairments and cognitive deficits overlapping with Frontotemporal Lobar Degeneration (FTLD). The etiology of ALS remains elusive, with various mechanisms and cellular targe...

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Autores principales: Amélie Poulin-Brière, Edris Rezaei, Silvia Pozzi
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:677940c8688947009b4e499213572c042021-12-01T13:58:55ZAntibody-Based Therapeutic Interventions for Amyotrophic Lateral Sclerosis: A Systematic Literature Review1662-453X10.3389/fnins.2021.790114https://doaj.org/article/677940c8688947009b4e499213572c042021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fnins.2021.790114/fullhttps://doaj.org/toc/1662-453XAmyotrophic Lateral Sclerosis (ALS) is a mid-life onset neurodegenerative disease that manifests its symptomatology with motor impairments and cognitive deficits overlapping with Frontotemporal Lobar Degeneration (FTLD). The etiology of ALS remains elusive, with various mechanisms and cellular targets implicated, and no treatment can reverse or stop the progression of the pathology. Therapeutic interventions based on passive immunization are gaining attention for neurodegenerative diseases, and FDA recently approved the first antibody-based approach for Alzheimer's disease. The present systematic review of the literature aims to highlight the efforts made over the past years at developing antibody-based strategies to cure ALS. Thirty-one original research papers have been selected where the therapeutic efficacy of antibodies were investigated and described in patients and animal models of ALS. Antibody-based interventions analyzed, target both extracellular molecules implicated in the pathology and intracellular pathogenic proteins known to drive the disease, such as SOD1, TDP-43 or C9ORF72 repeats expansions. The potentials and limitations of these therapeutic interventions have been described and discussed in the present review.Amélie Poulin-BrièreEdris RezaeiSilvia PozziSilvia PozziFrontiers Media S.A.articleamyotrophic lateral sclerosisantibody-based therapysystematic reviewknowledge synthesispassive immunizationNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571ENFrontiers in Neuroscience, Vol 15 (2021)
institution DOAJ
collection DOAJ
language EN
topic amyotrophic lateral sclerosis
antibody-based therapy
systematic review
knowledge synthesis
passive immunization
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
spellingShingle amyotrophic lateral sclerosis
antibody-based therapy
systematic review
knowledge synthesis
passive immunization
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Amélie Poulin-Brière
Edris Rezaei
Silvia Pozzi
Silvia Pozzi
Antibody-Based Therapeutic Interventions for Amyotrophic Lateral Sclerosis: A Systematic Literature Review
description Amyotrophic Lateral Sclerosis (ALS) is a mid-life onset neurodegenerative disease that manifests its symptomatology with motor impairments and cognitive deficits overlapping with Frontotemporal Lobar Degeneration (FTLD). The etiology of ALS remains elusive, with various mechanisms and cellular targets implicated, and no treatment can reverse or stop the progression of the pathology. Therapeutic interventions based on passive immunization are gaining attention for neurodegenerative diseases, and FDA recently approved the first antibody-based approach for Alzheimer's disease. The present systematic review of the literature aims to highlight the efforts made over the past years at developing antibody-based strategies to cure ALS. Thirty-one original research papers have been selected where the therapeutic efficacy of antibodies were investigated and described in patients and animal models of ALS. Antibody-based interventions analyzed, target both extracellular molecules implicated in the pathology and intracellular pathogenic proteins known to drive the disease, such as SOD1, TDP-43 or C9ORF72 repeats expansions. The potentials and limitations of these therapeutic interventions have been described and discussed in the present review.
format article
author Amélie Poulin-Brière
Edris Rezaei
Silvia Pozzi
Silvia Pozzi
author_facet Amélie Poulin-Brière
Edris Rezaei
Silvia Pozzi
Silvia Pozzi
author_sort Amélie Poulin-Brière
title Antibody-Based Therapeutic Interventions for Amyotrophic Lateral Sclerosis: A Systematic Literature Review
title_short Antibody-Based Therapeutic Interventions for Amyotrophic Lateral Sclerosis: A Systematic Literature Review
title_full Antibody-Based Therapeutic Interventions for Amyotrophic Lateral Sclerosis: A Systematic Literature Review
title_fullStr Antibody-Based Therapeutic Interventions for Amyotrophic Lateral Sclerosis: A Systematic Literature Review
title_full_unstemmed Antibody-Based Therapeutic Interventions for Amyotrophic Lateral Sclerosis: A Systematic Literature Review
title_sort antibody-based therapeutic interventions for amyotrophic lateral sclerosis: a systematic literature review
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/677940c8688947009b4e499213572c04
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AT silviapozzi antibodybasedtherapeuticinterventionsforamyotrophiclateralsclerosisasystematicliteraturereview
AT silviapozzi antibodybasedtherapeuticinterventionsforamyotrophiclateralsclerosisasystematicliteraturereview
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