Advances in Neurotrophic Factor and Cell-Based Therapies for Parkinson's Disease: A Mini-Review.
Identifieur interne : 001C97 ( Ncbi/Curation ); précédent : 001C96; suivant : 001C98Advances in Neurotrophic Factor and Cell-Based Therapies for Parkinson's Disease: A Mini-Review.
Auteurs : Michael D. Staudt [Canada] ; Andrea R. Di Sebastiano ; Hu Xu ; Mandar Jog ; Susanne Schmid ; Paula Foster ; Matthew O. HebbSource :
- Gerontology [ 1423-0003 ] ; 2016.
English descriptors
- KwdEn :
- Brain (metabolism), Cell- and Tissue-Based Therapy (methods), Dopamine (metabolism), Fetal Tissue Transplantation (methods), Genetic Vectors, Glial Cell Line-Derived Neurotrophic Factor (therapeutic use), Humans, Induced Pluripotent Stem Cells (transplantation), Mesencephalon (transplantation), Nerve Growth Factors (therapeutic use), Neurturin (therapeutic use), Parkinson Disease (metabolism), Parkinson Disease (therapy).
- MESH :
- chemical , metabolism : Dopamine.
- metabolism : Brain, Parkinson Disease.
- methods : Cell- and Tissue-Based Therapy, Fetal Tissue Transplantation.
- chemical , therapeutic use : Glial Cell Line-Derived Neurotrophic Factor, Nerve Growth Factors, Neurturin.
- therapy : Parkinson Disease.
- transplantation : Induced Pluripotent Stem Cells, Mesencephalon.
- Genetic Vectors, Humans.
Abstract
Parkinson's disease (PD) affects an estimated 7-10 million people worldwide and remains without definitive or disease-modifying treatment. There have been many recent developments in cell-based therapy (CBT) to replace lost circuitry and provide chronic biological sources of therapeutic agents to the PD-affected brain. Early neural transplantation studies underscored the challenges of immune compatibility, graft integration and the need for renewable, autologous graft sources. Neurotrophic factors (NTFs) offer a potential class of cytoprotective pharmacotherapeutics that may complement dopamine (DA) replacement and CBT strategies in PD. Chronic NTF delivery may be an integral goal of CBT, with grafts consisting of autologous drug-producing (e.g., DA, NTF) cells that are capable of integration and function in the host brain. In this mini-review, we outline the past experience and recent advances in NTF technology and CBT as promising and integrated approaches for the treatment of PD.
DOI: 10.1159/000438701
PubMed: 26330171
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pubmed:26330171Le document en format XML
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<term>Fetal Tissue Transplantation (methods)</term>
<term>Genetic Vectors</term>
<term>Glial Cell Line-Derived Neurotrophic Factor (therapeutic use)</term>
<term>Humans</term>
<term>Induced Pluripotent Stem Cells (transplantation)</term>
<term>Mesencephalon (transplantation)</term>
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<term>Neurturin (therapeutic use)</term>
<term>Parkinson Disease (metabolism)</term>
<term>Parkinson Disease (therapy)</term>
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<front><div type="abstract" xml:lang="en">Parkinson's disease (PD) affects an estimated 7-10 million people worldwide and remains without definitive or disease-modifying treatment. There have been many recent developments in cell-based therapy (CBT) to replace lost circuitry and provide chronic biological sources of therapeutic agents to the PD-affected brain. Early neural transplantation studies underscored the challenges of immune compatibility, graft integration and the need for renewable, autologous graft sources. Neurotrophic factors (NTFs) offer a potential class of cytoprotective pharmacotherapeutics that may complement dopamine (DA) replacement and CBT strategies in PD. Chronic NTF delivery may be an integral goal of CBT, with grafts consisting of autologous drug-producing (e.g., DA, NTF) cells that are capable of integration and function in the host brain. In this mini-review, we outline the past experience and recent advances in NTF technology and CBT as promising and integrated approaches for the treatment of PD.</div>
</front>
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