| Literature DB >> 29061445 |
Tomonori Iyoda1, Satoru Yamasaki1, Michihiro Hidaka2, Fumio Kawano2, Yu Abe3, Kenshi Suzuki3, Norimitsu Kadowaki4, Kanako Shimizu1, Shin-Ichiro Fujii5.
Abstract
NK cells represent a first line of immune defense, but are progressively dysregulated in multiple myeloma (MM) patients. To restore and facilitate their antitumor effect, NK cells are required in sufficient quantities and must be stimulated. We initially assessed the proportions of NKT and NK cells in 34 MM patients. The frequencies of both in PBMC populations correlated with those in BMMNCs irrespective of low BMMNC numbers. We then assessed the adjunctive effect of stimulating NKT cells with CD1d and α-GalCer complexes on the NK cells. The expression of NKG2D on CD56dimCD16+ NK cells and DNAM-1 on CD56brightCD16- NK cells increased after NKT cell activation. Apparently, NK cell-mediated anti-tumor effects were dependent on NKG2D and DNAM-1 ligands on myeloma cells. Thus, NK cell function in patients could be ameliorated, beyond the effect of immunosuppression, by NKT cell activation. This NKT-driven NK cell therapy could represent a potential new treatment modality.Entities:
Keywords: Innate immunity; Multiple myeloma; NK cells; NKT cells
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Year: 2017 PMID: 29061445 DOI: 10.1016/j.clim.2017.10.007
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969