Literature DB >> 35283274

Durability of transgene expression after rAAV gene therapy.

Manish Muhuri1, Daniel I Levy2, Martin Schulz3, Douglas McCarty2, Guangping Gao4.   

Abstract

Recombinant adeno-associated virus (rAAV) gene therapy has the potential to transform the lives of patients with certain genetic disorders by increasing or restoring function to affected tissues. Following the initial establishment of transgene expression, it is unknown how long the therapeutic effect will last, although animal and emerging human data show that expression can be maintained for more than 10 years. The durability of therapeutic response is key to long-term treatment success, especially since immune responses to rAAV vectors may prevent re-dosing with the same therapy. This review explores the non-immunological and immunological processes that may limit or improve durability and the strategies that can be used to increase the duration of the therapeutic effect.
Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  animals; gene expression; gene expression regulation; gene therapy; gene transfer techniques; genetic therapy/methods; genetic vectors; human genetics; transgenes

Mesh:

Year:  2022        PMID: 35283274      PMCID: PMC9077371          DOI: 10.1016/j.ymthe.2022.03.004

Source DB:  PubMed          Journal:  Mol Ther        ISSN: 1525-0016            Impact factor:   12.910


  154 in total

1.  A phase I study of an adeno-associated virus-CFTR gene vector in adult CF patients with mild lung disease.

Authors:  T Flotte; B Carter; C Conrad; W Guggino; T Reynolds; B Rosenstein; G Taylor; S Walden; R Wetzel
Journal:  Hum Gene Ther       Date:  1996-06-10       Impact factor: 5.695

2.  Differential and persistent expression patterns of CNS gene transfer by an adeno-associated virus (AAV) vector.

Authors:  T J McCown; X Xiao; J Li; G R Breese; R J Samulski
Journal:  Brain Res       Date:  1996-03-25       Impact factor: 3.252

Review 3.  Discussing investigational AAV gene therapy with hemophilia patients: A guide.

Authors:  Robert F Sidonio; Steven W Pipe; Michael U Callaghan; Leonard A Valentino; Paul E Monahan; Stacy E Croteau
Journal:  Blood Rev       Date:  2020-11-10       Impact factor: 8.250

4.  Effects of adeno-associated virus DNA hairpin structure on recombination.

Authors:  Vivian W Choi; R Jude Samulski; Douglas M McCarty
Journal:  J Virol       Date:  2005-06       Impact factor: 5.103

5.  CD8(+) T-cell responses to adeno-associated virus capsid in humans.

Authors:  Federico Mingozzi; Marcela V Maus; Daniel J Hui; Denise E Sabatino; Samuel L Murphy; John E J Rasko; Margaret V Ragni; Catherine S Manno; Jurg Sommer; Haiyan Jiang; Glenn F Pierce; Hildegund C J Ertl; Katherine A High
Journal:  Nat Med       Date:  2007-03-18       Impact factor: 53.440

6.  Prophylactic immune tolerance induced by changing the ratio of antigen-specific effector to regulatory T cells.

Authors:  S Nayak; O Cao; B E Hoffman; M Cooper; S Zhou; M A Atkinson; R W Herzog
Journal:  J Thromb Haemost       Date:  2009-07-06       Impact factor: 5.824

7.  A Guide to Creating and Testing New INTRSECT Constructs.

Authors:  Lief E Fenno; Joanna Mattis; Charu Ramakrishnan; Karl Deisseroth
Journal:  Curr Protoc Neurosci       Date:  2017-07-05

8.  Hepatotoxicity following administration of onasemnogene abeparvovec (AVXS-101) for the treatment of spinal muscular atrophy.

Authors:  Deepa Chand; Franziska Mohr; Hugh McMillan; Francis Fonyuy Tukov; Kyle Montgomery; Aaron Kleyn; Rui Sun; Sitra Tauscher-Wisniewski; Petra Kaufmann; Gerd Kullak-Ublick
Journal:  J Hepatol       Date:  2020-11-10       Impact factor: 25.083

9.  Five-Year Extension Results of the Phase 1 START Trial of Onasemnogene Abeparvovec in Spinal Muscular Atrophy.

Authors:  Jerry R Mendell; Samiah A Al-Zaidy; Kelly J Lehman; Markus McColly; Linda P Lowes; Lindsay N Alfano; Natalie F Reash; Megan A Iammarino; Kathleen R Church; Aaron Kleyn; Matthew N Meriggioli; Richard Shell
Journal:  JAMA Neurol       Date:  2021-07-01       Impact factor: 18.302

10.  Subretinal Injection of HY Peptides Induces Systemic Antigen-Specific Inhibition of Effector CD4+ and CD8+ T-Cell Responses.

Authors:  Julie Vendomèle; Safa Dehmani; Quentin Khebizi; Anne Galy; Sylvain Fisson
Journal:  Front Immunol       Date:  2018-03-13       Impact factor: 7.561

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