Genetic modification of primary natural killer cells overcomes inhibitory signals and induces specific killing of leukemic cells
St. Jude Children's Research Hospital · University of Tennessee Health Science Center
Abstract
Natural killer (NK) cells hold promise for improving the therapeutic potential of allogeneic hematopoietic transplantation, but their effectiveness is limited by inhibitory HLA types. We sought to overcome this intrinsic resistance by transducing CD56+CD3- NK cells with chimeric receptors directed against CD19, a molecule widely expressed by malignant B cells. An abundance of NK cells for transduction was secured by culturing peripheral blood mononuclear cells with K562 cells expressing the NK-stimulatory molecules 4-1BB ligand and interleukin 15, which yielded a median greater than 1000-fold expansion of CD56+CD3- cells at 3 weeks of culture, without T-lymphocyte expansion. Expression of anti-CD19 receptors…
Citation impact
- FWCI
- 5.28
- Percentile
- 100%
- References
- 71
Authors
3- CIChihaya ImaiCorresponding
St. Jude Children's Research Hospital, University of Tennessee Health Science Center
- SIShotaro Iwamoto
St. Jude Children's Research Hospital, University of Tennessee Health Science Center
- DCDario Campana
St. Jude Children's Research Hospital, University of Tennessee Health Science Center
Topics & keywords
- Interleukin 12
- Interleukin 21
- Biology
- Lymphokine-activated killer cell
- Janus kinase 3
- NK-92
- Receptor
- Cell biology