Adapter-Mediated Transduction with Lentiviral Vectors: A Novel Tool for Cell-Type-Specific Gene Transfer

Selective gene delivery to a cell type of interest utilizing targeted lentiviral vectors (LVs) is an efficient and safe strategy for cell and gene therapy applications, including chimeric antigen receptor (CAR)-T cell therapy. LVs pseudotyped with measles virus envelope proteins (MV-LVs) have been r...

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Detalles Bibliográficos
Autores principales: Cordes, Nicole, Winter, Nora, Kolbe, Carolin, Kotter, Bettina, Mittelstaet, Joerg, Assenmacher, Mario, Cathomen, Toni, Kaiser, Andrew, Schaser, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9607492/
https://www.ncbi.nlm.nih.gov/pubmed/36298713
http://dx.doi.org/10.3390/v14102157

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9607492/
https://www.ncbi.nlm.nih.gov/pubmed/36298713
http://dx.doi.org/10.3390/v14102157

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