Reduction of liver macrophage transduction by pseudotyping lentiviral vectors with a fusion envelope from Autographa californica GP64 and Sendai virus F2 domain

BACKGROUND: Lentiviral vectors are well suited for gene therapy because they can mediate long-term expression in both dividing and nondividing cells. However, lentiviral vectors seem less suitable for liver gene therapy because systemically administered lentiviral vectors are preferentially sequeste...

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Detalles Bibliográficos
Autores principales: Markusic, David M, van Til, Niek P, Hiralall, Johan K, Elferink, Ronald PJ Oude, Seppen, Jurgen
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762966/
https://www.ncbi.nlm.nih.gov/pubmed/19811629
http://dx.doi.org/10.1186/1472-6750-9-85

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2762966/
https://www.ncbi.nlm.nih.gov/pubmed/19811629
http://dx.doi.org/10.1186/1472-6750-9-85

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