CDNF Protein Therapy in Parkinson’s Disease

Neurotrophic factors (NTF) are a subgroup of growth factors that promote survival and differentiation of neurons. Due to their neuroprotective and neurorestorative properties, their therapeutic potential has been tested in various neurodegenerative diseases. Bioavailability of NTFs in the target tis...

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Main Authors: Henri J. Huttunen, Mart Saarma
Format: Article
Language:English
Published: SAGE Publishing 2019-04-01
Series:Cell Transplantation
Online Access:https://doi.org/10.1177/0963689719840290
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spelling doaj-29daf89731b44eaf92deacb85d31cf3b2020-11-25T03:35:23ZengSAGE PublishingCell Transplantation0963-68971555-38922019-04-012810.1177/0963689719840290CDNF Protein Therapy in Parkinson’s DiseaseHenri J. Huttunen0Mart Saarma1 Neuroscience Center, HiLIFE, University of Helsinki, Helsinki, Finland Institute of Biotechnology, HiLIFE, University of Helsinki, Helsinki, FinlandNeurotrophic factors (NTF) are a subgroup of growth factors that promote survival and differentiation of neurons. Due to their neuroprotective and neurorestorative properties, their therapeutic potential has been tested in various neurodegenerative diseases. Bioavailability of NTFs in the target tissue remains a major challenge for NTF-based therapies. Various intracerebral delivery approaches, both protein and gene transfer-based, have been tested with varying outcomes. Three growth factors, glial cell-line derived neurotrophic factor (GDNF), neurturin (NRTN) and platelet-derived growth factor (PDGF-BB) have been tested in clinical trials in Parkinson’s disease (PD) during the past 20 years. A new protein can now be added to this list, as cerebral dopamine neurotrophic factor (CDNF) has recently entered clinical trials. Despite their misleading names, CDNF, together with its closest relative mesencephalic astrocyte-derived neurotrophic factor (MANF), form a novel family of unconventional NTF that are both structurally and mechanistically distinct from other growth factors. CDNF and MANF are localized mainly to the lumen of endoplasmic reticulum (ER) and their primary function appears to be modulation of the unfolded protein response (UPR) pathway. Prolonged ER stress, via the UPR signaling pathways, contributes to the pathogenesis in a number of chronic degenerative diseases, and is an important target for therapeutic modulation. Intraputamenally administered recombinant human CDNF has shown robust neurorestorative effects in a number of small and large animal models of PD, and had a good safety profile in preclinical toxicology studies. Intermittent monthly bilateral intraputamenal infusions of CDNF are currently being tested in a randomized placebo-controlled phase I–II clinical study in moderately advanced PD patients. Here, we review the history of growth factor-based clinical trials in PD, and discuss how CDNF differs from the previously tested growth factors.https://doi.org/10.1177/0963689719840290
collection DOAJ
language English
format Article
sources DOAJ
author Henri J. Huttunen
Mart Saarma
spellingShingle Henri J. Huttunen
Mart Saarma
CDNF Protein Therapy in Parkinson’s Disease
Cell Transplantation
author_facet Henri J. Huttunen
Mart Saarma
author_sort Henri J. Huttunen
title CDNF Protein Therapy in Parkinson’s Disease
title_short CDNF Protein Therapy in Parkinson’s Disease
title_full CDNF Protein Therapy in Parkinson’s Disease
title_fullStr CDNF Protein Therapy in Parkinson’s Disease
title_full_unstemmed CDNF Protein Therapy in Parkinson’s Disease
title_sort cdnf protein therapy in parkinson’s disease
publisher SAGE Publishing
series Cell Transplantation
issn 0963-6897
1555-3892
publishDate 2019-04-01
description Neurotrophic factors (NTF) are a subgroup of growth factors that promote survival and differentiation of neurons. Due to their neuroprotective and neurorestorative properties, their therapeutic potential has been tested in various neurodegenerative diseases. Bioavailability of NTFs in the target tissue remains a major challenge for NTF-based therapies. Various intracerebral delivery approaches, both protein and gene transfer-based, have been tested with varying outcomes. Three growth factors, glial cell-line derived neurotrophic factor (GDNF), neurturin (NRTN) and platelet-derived growth factor (PDGF-BB) have been tested in clinical trials in Parkinson’s disease (PD) during the past 20 years. A new protein can now be added to this list, as cerebral dopamine neurotrophic factor (CDNF) has recently entered clinical trials. Despite their misleading names, CDNF, together with its closest relative mesencephalic astrocyte-derived neurotrophic factor (MANF), form a novel family of unconventional NTF that are both structurally and mechanistically distinct from other growth factors. CDNF and MANF are localized mainly to the lumen of endoplasmic reticulum (ER) and their primary function appears to be modulation of the unfolded protein response (UPR) pathway. Prolonged ER stress, via the UPR signaling pathways, contributes to the pathogenesis in a number of chronic degenerative diseases, and is an important target for therapeutic modulation. Intraputamenally administered recombinant human CDNF has shown robust neurorestorative effects in a number of small and large animal models of PD, and had a good safety profile in preclinical toxicology studies. Intermittent monthly bilateral intraputamenal infusions of CDNF are currently being tested in a randomized placebo-controlled phase I–II clinical study in moderately advanced PD patients. Here, we review the history of growth factor-based clinical trials in PD, and discuss how CDNF differs from the previously tested growth factors.
url https://doi.org/10.1177/0963689719840290
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