No Impact of Lentiviral Transduction on Hematopoietic Stem/Progenitor Cell Telomere Length or Gene Expression in the Rhesus Macaque Model-Reference-Cited by-同舟云学术

No Impact of Lentiviral Transduction on Hematopoietic Stem/Progenitor Cell Telomere Length or Gene Expression in the Rhesus Macaque Model

Published:2014-01 Issue:1 Volume:22 Page:52-58
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Sellers Stephanie E,Dumitriu Bogdan,Morgan Mary J,Hughes William M.,Wu Colin O,Raghavarchari Nalini,Yang Yanqin,Uchida Naoya,Tisdale John F,An Dong S,Chen Irvin S,Hematti Peiman,Donahue Robert E,LaRochelle Andre,Young Neal S,Calado Rodrigo T,Dunbar Cynthia E

Publisher

Elsevier BV

Subject

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

Reference49 articles.

1. Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease;Cavazzana-Calvo;Science,2000

2. LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1;Hacein-Bey-Abina;Science,2003

3. Genotoxicity of retroviral integration in hematopoietic cells;Nienhuis;Mol Ther,2006

4. Hematopoietic stem cell gene therapy: dead or alive?;Ferguson;Trends Biotechnol,2005

5. Challenges in vector and trial design using retroviral vectors for long-term gene correction in hematopoietic stem cell gene therapy;Corrigan-Curay;Mol Ther,2012

Cited by 4 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. Barcode clonal tracking of tissue-resident immune cells in rhesus macaque highlights distinct clonal distribution pattern of tissue NK cells;Frontiers in Immunology;2022-11-10

2. Lentiviral vectors escape innate sensing but trigger p53 in human hematopoietic stem and progenitor cells;EMBO Molecular Medicine;2017-06-30

3. Cellular Innate Immunity and Restriction of Viral Infection: Implications for Lentiviral Gene Therapy in Human Hematopoietic Cells;Human Gene Therapy;2015-04

4. Pigtailed macaques as a model to study long-term safety of lentivirus vector-mediated gene therapy for hemoglobinopathies;Molecular Therapy - Methods & Clinical Development;2014