Flushing Out Antibodies to Make AAV Gene Therapy Available to More Patients
Author:
Publisher
Elsevier BV
Subject
Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine
Reference17 articles.
1. The gene therapy journey for hemophilia: are we there yet?;High;Blood,2012
2. Adenovirus-associated virus vector–mediated gene transfer in hemophilia B;Nathwani;N Engl J Med,2011
3. The pleiotropic effects of natural AAV infections on liver-directed gene transfer in macaques;Wang;Mol Ther,2010
4. Impact of pre-existing immunity on gene transfer to nonhuman primate liver with adeno-associated virus 8 vectors;Wang;Hum Gene Ther,2011
5. Minimizing the inhibitory effect of neutralizing antibody for efficient gene expression in the liver with adeno-associated virus 8 vectors;Mimuro;Mol Ther,2013
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Immunogenicity of Recombinant Adeno-Associated Virus (AAV) Vectors for Gene Transfer;BioDrugs;2023-03-02
2. Obstacles and future of gene therapy for hemophilia;Expert Opinion on Orphan Drugs;2015-07-18
3. Immune System Obstacles to In vivo Gene Transfer with Adeno-Associated Virus Vectors;Translating Gene Therapy to the Clinic;2015
4. Gene Therapy to Treat Cardiovascular Disease;Journal of the American Heart Association;2013-08-22
5. Pre-existing Anti–Adeno-Associated Virus Antibodies as a Challenge in AAV Gene Therapy;Human Gene Therapy Methods;2013-04
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