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dc.contributor.authorMuhuri, Manish
dc.contributor.authorLevy, Daniel I
dc.contributor.authorSchulz, Martin
dc.contributor.authorMcCarty, Douglas
dc.contributor.authorGao, Guangping
dc.date.accessioned2023-08-10T20:18:55Z
dc.date.available2023-08-10T20:18:55Z
dc.date.issued2022-03-10
dc.identifier.citationMuhuri M, Levy DI, Schulz M, McCarty D, Gao G. Durability of transgene expression after rAAV gene therapy. Mol Ther. 2022 Apr 6;30(4):1364-1380. doi: 10.1016/j.ymthe.2022.03.004. Epub 2022 Mar 10. PMID: 35283274; PMCID: PMC9077371.en_US
dc.identifier.eissn1525-0024
dc.identifier.doi10.1016/j.ymthe.2022.03.004en_US
dc.identifier.pmid35283274
dc.identifier.urihttp://hdl.handle.net/20.500.14038/52405
dc.description.abstractRecombinant 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.en_US
dc.language.isoenen_US
dc.relation.ispartofMolecular Therapyen_US
dc.relation.urlhttps://doi.org/10.1016/j.ymthe.2022.03.004en_US
dc.rightsCopyright 2022 The Author(s). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectanimalsen_US
dc.subjectgene expressionen_US
dc.subjectgene expression regulationen_US
dc.subjectgene therapyen_US
dc.subjectgene transfer techniquesen_US
dc.subjectgenetic therapy/methodsen_US
dc.subjectgenetic vectorsen_US
dc.subjecthuman geneticsen_US
dc.subjecttransgenesen_US
dc.titleDurability of transgene expression after rAAV gene therapyen_US
dc.typeJournal Articleen_US
dc.source.journaltitleMolecular therapy : the journal of the American Society of Gene Therapy
dc.source.volume30
dc.source.issue4
dc.source.beginpage1364
dc.source.endpage1380
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.identifier.journalMolecular therapy : the journal of the American Society of Gene Therapy
refterms.dateFOA2023-08-10T20:18:56Z
dc.contributor.departmentHorae Gene Therapy Centeren_US
dc.contributor.departmentLi Weibo Institute for Rare Diseases Researchen_US
dc.contributor.departmentMicrobiology and Physiological Systemsen_US


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Copyright 2022 The Author(s).
This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Except where otherwise noted, this item's license is described as Copyright 2022 The Author(s). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).