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A novel adeno-assoc...
A novel adeno-associated virus capsid with enhanced neurotropism corrects a lysosomal transmembrane enzyme deficiency
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- Tordo, Julie (författare)
- King's College London
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- O'Leary, Claire (författare)
- University of Manchester
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- Antunes, André S.L.M. (författare)
- King's College London
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- Palomar, Nuria (författare)
- King's College London
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- Aldrin-Kirk, Patrick (författare)
- Lund University,Lunds universitet,Molekylär neuromodulering,Forskargrupper vid Lunds universitet,Molecular Neuromodulation,Lund University Research Groups
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- Basche, Mark (författare)
- University College London
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- Bennett, Antonette (författare)
- Florida Museum Natural History
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- D'Souza, Zelpha (författare)
- University of Manchester
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- Gleitz, Hélène (författare)
- University of Manchester
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- Godwin, Annie (författare)
- University of Manchester
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- Holley, Rebecca J. (författare)
- University of Manchester
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- Parker, Helen (författare)
- University of Manchester
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- Liao, Ai Yin (författare)
- University of Manchester
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- Rouse, Paul (författare)
- University of Manchester
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- Youshani, Amir Saam (författare)
- University of Manchester
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- Dridi, Larbi (författare)
- Centre Hospitalier Universitaire Sainte-Justine
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- Martins, Carla (författare)
- Centre Hospitalier Universitaire Sainte-Justine
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- Levade, Thierry (författare)
- Toulouse University Hospital
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- Stacey, Kevin B. (författare)
- University of Manchester
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- Davis, Daniel M. (författare)
- University of Manchester
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- Dyer, Adam (författare)
- King's College London
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- Clément, Nathalie (författare)
- Florida Museum Natural History
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- Björklund, Tomas (författare)
- Lund University,Lunds universitet,Molekylär neuromodulering,Forskargrupper vid Lunds universitet,Molecular Neuromodulation,Lund University Research Groups
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- Ali, Robin R. (författare)
- University College London
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- Agbandje-McKenna, Mavis (författare)
- Florida Museum Natural History
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- Rahim, Ahad A. (författare)
- University College London
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- Pshezhetsky, Alexey (författare)
- Centre Hospitalier Universitaire Sainte-Justine
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- Waddington, Simon N. (författare)
- University of the Witwatersrand,University College London
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- Linden, R. Michael (författare)
- King's College London
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- Bigger, Brian W. (författare)
- University of Manchester
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- Henckaerts, Els (författare)
- King's College London
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(creator_code:org_t)
- 2018-05-16
- 2018
- Engelska 18 s.
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Ingår i: Brain. - : Oxford University Press (OUP). - 0006-8950 .- 1460-2156. ; 141:7, s. 2014-2031
- Relaterad länk:
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http://dx.doi.org/10... (free)
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https://academic.oup...
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https://lup.lub.lu.s...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- Recombinant adeno-associated viruses (AAVs) are popular in vivo gene transfer vehicles. However, vector doses needed to achieve therapeutic effect are high and some target tissues in the central nervous system remain difficult to transduce. Gene therapy trials using AAV for the treatment of neurological disorders have seldom led to demonstrated clinical efficacy. Important contributing factors are low transduction rates and inefficient distribution of the vector. To overcome these hurdles, a variety of capsid engineering methods have been utilized to generate capsids with improved transduction properties. Here we describe an alternative approach to capsid engineering, which draws on the natural evolution of the virus and aims to yield capsids that are better suited to infect human tissues. We generated an AAV capsid to include amino acids that are conserved among natural AAV2 isolates and tested its biodistribution properties in mice and rats. Intriguingly, this novel variant, AAV-TT, demonstrates strong neurotropism in rodents and displays significantly improved distribution throughout the central nervous system as compared to AAV2. Additionally, sub-retinal injections in mice revealed markedly enhanced transduction of photoreceptor cells when compared to AAV2. Importantly, AAV-TT exceeds the distribution abilities of benchmark neurotropic serotypes AAV9 and AAVrh10 in the central nervous system of mice, and is the only virus, when administered at low dose, that is able to correct the neurological phenotype in a mouse model of mucopolysaccharidosis IIIC, a transmembrane enzyme lysosomal storage disease, which requires delivery to every cell for biochemical correction. These data represent unprecedented correction of a lysosomal transmembrane enzyme deficiency in mice and suggest that AAV-TT-based gene therapies may be suitable for treatment of human neurological diseases such as mucopolysaccharidosis IIIC, which is characterized by global neuropathology.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
Nyckelord
- adeno-associated virus
- capsid engineering
- lysosomal transmembrane enzyme
- mucopolysaccharidosis
- neurotropism
Publikations- och innehållstyp
- art (ämneskategori)
- ref (ämneskategori)
Hitta via bibliotek
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Brain
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Till lärosätets databas
- Av författaren/redakt...
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Tordo, Julie
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O'Leary, Claire
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Antunes, André S ...
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Palomar, Nuria
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Aldrin-Kirk, Pat ...
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Basche, Mark
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visa fler...
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Bennett, Antonet ...
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D'Souza, Zelpha
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Gleitz, Hélène
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Godwin, Annie
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Holley, Rebecca ...
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Parker, Helen
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Liao, Ai Yin
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Rouse, Paul
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Youshani, Amir S ...
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Dridi, Larbi
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Martins, Carla
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Levade, Thierry
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Stacey, Kevin B.
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Davis, Daniel M.
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Dyer, Adam
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Clément, Nathali ...
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Björklund, Tomas
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Ali, Robin R.
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Agbandje-McKenna ...
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Rahim, Ahad A.
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Pshezhetsky, Ale ...
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Waddington, Simo ...
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Linden, R. Micha ...
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Bigger, Brian W.
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Henckaerts, Els
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