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Reprogramming human T cell function and specificity with non-viral genome targeting
Decades of work have aimed to genetically reprogram T cells for therapeutic purposes(1) using recombinant viral vectors, which do not target transgenes to specific genomic sites(2,3). In addition, the need for viral vectors has slowed down research and clinical use as their manufacturing and testing...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6239417/ https://www.ncbi.nlm.nih.gov/pubmed/29995861 http://dx.doi.org/10.1038/s41586-018-0326-5 |