Targeting multiple types of tumors using NKG2D-coated iron oxide nanoparticles

被引:5
作者
Wu, Ming-Ru [1 ]
Cook, W. James [1 ]
Zhang, Tong [1 ]
Sentman, Charles L. [1 ]
机构
[1] Geisel Sch Med Dartmouth, Dept Microbiol & Immunol, Lebanon, NH USA
关键词
nanoparticles; NKG2D; lymphoma; ovarian cancer; MICA; Rae-1; CHIMERIC NKG2D RECEPTOR; NKG2D-MODIFIED T-CELLS; MAGNETIC NANOPARTICLES; CANCER-THERAPY; CONTRAST AGENTS; OVARIAN-CANCER; BREAST-CANCER; HYPERTHERMIA; MRI;
D O I
10.1088/0957-4484/25/47/475101
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Iron oxide nanoparticles (IONPs) hold great potential for cancer therapy. Actively targeting IONPs to tumor cells can further increase therapeutic efficacy and decrease off-target side effects. To target tumor cells, a natural killer (NK) cell activating receptor, NKG2D, was utilized to develop pan-tumor targeting IONPs. NKG2D ligands are expressed on many tumor types and its ligands are not found on most normal tissues under steady state conditions. The data showed that mouse and human fragment crystallizable (Fc)-fusion NKG2D (Fc-NKG2D) coated IONPs (NKG2D/NPs) can target multiple NKG2D ligand positive tumor types in vitro in a dose dependent manner by magnetic cell sorting. Tumor targeting effect was robust even under a very low tumor cell to normal cell ratio and targeting efficiency correlated with NKG2D ligand expression level on tumor cells. Furthermore, the magnetic separation platform utilized to test NKG2D/NP specificity has the potential to be developed into high throughput screening strategies to identify ideal fusion proteins or antibodies for targeting IONPs. In conclusion, NKG2D/NPs can be used to target multiple tumor types and magnetic separation platform can facilitate the proof-of-concept phase of tumor targeting IONP development.
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页数:10
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