Near infrared photoimmunotherapy with avelumab, an antiprogrammed death-ligand 1 (PD-L1) antibody

被引:72
作者
Nagaya, Tadanobu [1 ]
Nakamura, Yuko [1 ]
Sato, Kazuhide [1 ]
Harada, Toshiko [1 ]
Choyke, Peter L. [1 ]
Hodge, James W. [2 ]
Schlom, Jeffrey [2 ]
Kobayashi, Hisataka [1 ]
机构
[1] NCI, Mol Imaging Program, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bldg 10, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
near infrared photoimmunotherapy; PD-L1; lung cancer; ANTI-PD-L1; ANTIBODY; ENHANCED PERMEABILITY; INTERFERON-GAMMA; LUNG-CANCER; TUMOR-CELLS; MELANOMA; METASTASIS; EXPRESSION; SAFETY; MODEL;
D O I
10.18632/oncotarget.12410
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Near Infrared-Photoimmunotherapy (NIR-PIT) is a highly selective tumor treatment that employs an antibody-photo-absorber conjugate (APC). Programmed cell death protein-1 ligand (PD-L1) is emerging as a molecular target. Here, we describe the efficacy of NIR-PIT, using fully human IgG1 anti-PD-L1 monoclonal antibody (mAb), avelumab, conjugated to the photo-absorber, IR700DX, in a PD-L1 expressing H441 cell line, papillary adenocarcinoma of lung. Avelumab-IR700 showed specific binding and cell-specific killing was observed after exposure of the cells to NIR in vitro. In the in vivo study, avelumab-IR700 showed high tumor accumulation and high tumor-background ratio. Tumor-bearing mice were separated into 4 groups: (1) no treatment; (2) 100 mu g of avelumab-IR700 i.v.; (3) NIR light exposure only, NIR light was administered; (4) 100 mu g of avelumab-IR700 i.v., NIR light was administered. Tumor growth was significantly inhibited by NIR-PIT treatment compared with the other groups (p < 0.001), and significantly prolonged survival was achieved (p < 0.01 vs other groups). In conclusion, the anti-PD-L1 antibody, avelumab, is suitable as an APC for NIR-PIT. Furthermore, NIR-PIT with avelumab-IR700 is a promising candidate of the treatment of PD-L1-expressing tumors that could be readily translated to humans.
引用
收藏
页码:8807 / 8817
页数:11
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