scholarly journals Parkinson's disease gene therapy: Will focused ultrasound and nanovectors be the next frontier?

2019 ◽  
Vol 34 (9) ◽  
pp. 1279-1282 ◽  
Author(s):  
Richard J. Price ◽  
Delaney G. Fisher ◽  
Jung Soo Suk ◽  
Justin Hanes ◽  
Han Seok Ko ◽  
...  
Viruses ◽  
2014 ◽  
Vol 6 (8) ◽  
pp. 3293-3310 ◽  
Author(s):  
Travis Lewis ◽  
Joel Glasgow ◽  
Ashley Harms ◽  
David Standaert ◽  
David Curiel

Nano Letters ◽  
2017 ◽  
Vol 17 (6) ◽  
pp. 3533-3542 ◽  
Author(s):  
Brian P. Mead ◽  
Namho Kim ◽  
G. Wilson Miller ◽  
David Hodges ◽  
Panagiotis Mastorakos ◽  
...  

2021 ◽  
pp. 1-8
Author(s):  
Paul S. Larson

A number of cell transplantation and gene therapy trials have been performed over the last three decades in an effort to restore function in Parkinson’s disease. Much has been learned about optimizing delivery methods for these therapeutics. This is particularly true in gene therapy, which has predominated the clinical trial landscape in recent years; however, cell transplantation for Parkinson’s disease is currently undergoing a renaissance. Innovations such as cannula design, iMRI-guided surgery and an evolution in delivery strategy has radically changed the way investigators approach clinical trial design. Future therapeutic strategies may employ newer delivery methods such as chronically implanted infusion devices and focal opening of the blood brain barrier with focused ultrasound.


2014 ◽  
Vol 22 (3) ◽  
pp. 487-497 ◽  
Author(s):  
Raymond T Bartus ◽  
Marc S Weinberg ◽  
R. Jude Samulski

2005 ◽  
Vol 32 (S 4) ◽  
Author(s):  
A.H Jacobs ◽  
R Hilker ◽  
L Burghaus ◽  
W.D Heiss

2021 ◽  
pp. 1-7
Author(s):  
Sarah Jarrin ◽  
Abrar Hakami ◽  
Ben Newland ◽  
Eilís Dowd

Despite decades of research and billions in global investment, there remains no preventative or curative treatment for any neurodegenerative condition, including Parkinson’s disease (PD). Arguably, the most promising approach for neuroprotection and neurorestoration in PD is using growth factors which can promote the growth and survival of degenerating neurons. However, although neurotrophin therapy may seem like the ideal approach for neurodegenerative disease, the use of growth factors as drugs presents major challenges because of their protein structure which creates serious hurdles related to accessing the brain and specific targeting of affected brain regions. To address these challenges, several different delivery systems have been developed, and two major approaches—direct infusion of the growth factor protein into the target brain region and in vivo gene therapy—have progressed to clinical trials in patients with PD. In addition to these clinically evaluated approaches, a range of other delivery methods are in various degrees of development, each with their own unique potential. This review will give a short overview of some of these alternative delivery systems, with a focus on ex vivo gene therapy and biomaterial-aided protein and gene delivery, and will provide some perspectives on their potential for clinical development and translation.


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