Targeting the lung epithelium after intravenous delivery by directed evolution of underexplored sites on the AAV capsid-Reference-Cited by-同舟云学术

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Targeting the lung epithelium after intravenous delivery by directed evolution of underexplored sites on the AAV capsid

Published:2022-09 Issue: Volume:26 Page:331-342
ISSN:2329-0501
Container-title:Molecular Therapy - Methods & Clinical Development
language:en
Short-container-title:Molecular Therapy - Methods & Clinical Development

Author:

Goertsen David^ORCID,Goeden Nick,Flytzanis Nicholas C.,Gradinaru Viviana^ORCID

Funder

Defense Advanced Research Projects Agency

Cystic Fibrosis Foundation

Natural Sciences and Engineering Research Council of Canada

National Institutes of Health

Publisher

Elsevier BV

Subject

Genetics,Molecular Biology,Molecular Medicine

Reference85 articles.

1. Gene therapy using adeno-associated virus vectors;Daya;Clin. Microbiol. Rev.,2008

2. Long-term expression and repeated administration of AAV type 1, 2 and 5 vectors in skeletal muscle of immunocompetent adult mice;Rivière;Gene Ther.,2006

3. Adeno-associated virus (AAV) as a vector for gene therapy;Naso;BioDrugs,2017

4. Gene therapy for lipoprotein lipase deficiency;Gaudet;Curr. Opin. Lipidol.,2012

5. The clinical landscape for AAV gene therapies;Kuzmin;Nat. Rev. Drug Discov.,2021

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1. Recent Advances in Therapeutics and Manufacturing Processes of Recombinant Adeno-Associated Virus for the Treatment of Lung Diseases;Current Gene Therapy;2024-09-02

2. Adeno-associated virus–based gene therapy treats inflammatory kidney disease in mice;Journal of Clinical Investigation;2024-08-15

3. Microglia targeting by adeno-associated viral vectors;Frontiers in Immunology;2024-07-05

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