Cargando…
Comparison of Lentiviral and Sleeping Beauty Mediated αβ T Cell Receptor Gene Transfer
Transfer of tumour antigen-specific receptors to T cells requires efficient delivery and integration of transgenes, and currently most clinical studies are using gamma retroviral or lentiviral systems. Whilst important proof-of-principle data has been generated for both chimeric antigen receptors an...
Autores principales: | Field, Anne-Christine, Vink, Conrad, Gabriel, Richard, Al-Subki, Roua, Schmidt, Manfred, Goulden, Nicholas, Stauss, Hans, Thrasher, Adrian, Morris, Emma, Qasim, Waseem |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695921/ https://www.ncbi.nlm.nih.gov/pubmed/23840834 http://dx.doi.org/10.1371/journal.pone.0068201 |
Ejemplares similares
-
Lentiviral Vector Production Titer Is Not Limited in HEK293T by Induced Intracellular Innate Immunity
por: Ferreira, Carolina B., et al.
Publicado: (2019) -
Lentiviral Gene Transfer Corrects Immune Abnormalities in XIAP Deficiency
por: Topal, Joseph, et al.
Publicado: (2022) -
Lentiviral vectors can be used for full-length dystrophin gene therapy
por: Counsell, John R., et al.
Publicado: (2017) -
Lentiviral vectors can be used for full-length dystrophin gene therapy
por: Counsell, John R., et al.
Publicado: (2017) -
Erratum: Lentiviral vectors can be used for full-length dystrophin gene therapy
por: Counsell, John R., et al.
Publicado: (2017)