| Literature DB >> 27177671 |
Emily Lowe1, Laurel C Truscott2,3, Satiro N De Oliveira4,5.
Abstract
NK cells represent a very promising source for adoptive cellular approaches for cancer immunotherapy, and extensive research has been conducted, including clinical trials. Gene modification of NK cells can direct their specificity and enhance their function, but the efficiency of gene transfer techniques is very limited. Here we describe two protocols designed to generate mature human NK cells from gene-modified hematopoietic stem cells. These protocols use chimeric antigen receptor as the transgene, but could potentially be modified for the expression any particular transgene in human NK cells.Entities:
Keywords: Gene transfer; Hematopoietic stem cells; Lentiviral vector; NK cells; OP9 cell line
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Year: 2016 PMID: 27177671 PMCID: PMC5065352 DOI: 10.1007/978-1-4939-3684-7_20
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745