Binding and neutralizing anti-AAV antibodies: Detection and implications for rAAV-mediated gene therapy-Reference-Cited by-同舟云学术

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Binding and neutralizing anti-AAV antibodies: Detection and implications for rAAV-mediated gene therapy

Published:2023-03 Issue:3 Volume:31 Page:616-630
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Schulz Martin,Levy Daniel I.,Petropoulos Christos J.,Bashirians George,Winburn Ian,Mahn Matthias,Somanathan Suryanarayan,Cheng Seng H.,Byrne Barry J.

Funder

Pfizer

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

Reference138 articles.

1. Current and future prospects for gene therapy for rare genetic diseases affecting the brain and spinal cord;Jensen;Front. Mol. Neurosci.,2021

2. Gene therapy for monogenic liver diseases: clinical successes, current challenges and future prospects;Baruteau;J. Inherit. Metab. Dis.,2017

3. Adeno-associated virus vector as a platform for gene therapy delivery;Wang;Nat. Rev. Drug Discov.,2019

4. Evolutionary relationships among parvoviruses: virus-host coevolution among autonomous primate parvoviruses and links between adeno-associated and avian parvoviruses;Lukashov;J. Virol.,2001

5. Adeno-associated virus-mediated IL-10 gene transfer suppresses lacrimal gland immunopathology in a rabbit model of autoimmune dacryoadenitis;Thomas;Invest. Ophthalmol. Vis. Sci.,2010

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