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Efficient and Highly Specific Gene Transfer Using Mutated Lentiviral Vectors Redirected with Bispecific Antibodies
Despite their exceptional potencies, the broad tropism of most commonly used lentivirus (LV) vectors limits their use for targeted gene delivery in vivo. We hypothesized that we could improve the specificity of LV targeting by coupling (i) reduction of their binding to off-target cells with (ii) red...
Autores principales: | Parker, Christina L., Jacobs, Timothy M., Huckaby, Justin T., Harit, Dimple, Lai, Samuel K. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6989108/ https://www.ncbi.nlm.nih.gov/pubmed/31964730 http://dx.doi.org/10.1128/mBio.02990-19 |
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