Suppr超能文献

使用抗程序性死亡配体1(PD-L1)抗体阿维鲁单抗进行近红外光免疫治疗。

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

作者信息

Nagaya Tadanobu, Nakamura Yuko, Sato Kazuhide, Harada Toshiko, Choyke Peter L, Hodge James W, Schlom Jeffrey, Kobayashi Hisataka

机构信息

Molecular Imaging Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, United States of America.

Laboratory of Tumor Immunology and Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, United States of America.

出版信息

Oncotarget. 2017 Jan 31;8(5):8807-8817. doi: 10.18632/oncotarget.12410.

Abstract

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 μg of avelumab-IR700 i.v.; (3) NIR light exposure only, NIR light was administered; (4) 100 μg 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.

摘要

近红外光免疫疗法(NIR-PIT)是一种高度选择性的肿瘤治疗方法,它采用抗体-光吸收剂偶联物(APC)。程序性细胞死亡蛋白1配体(PD-L1)正成为一个分子靶点。在此,我们描述了在表达PD-L1的肺乳头状腺癌H441细胞系中,使用与光吸收剂IR700DX偶联的全人IgG1抗PD-L1单克隆抗体(mAb)阿维鲁单抗进行NIR-PIT的疗效。阿维鲁单抗-IR700显示出特异性结合,并且在体外将细胞暴露于近红外光后观察到细胞特异性杀伤。在体内研究中,阿维鲁单抗-IR700显示出高肿瘤蓄积和高肿瘤-背景比。荷瘤小鼠被分为4组:(1)不治疗;(2)静脉注射100μg阿维鲁单抗-IR700;(3)仅近红外光照射;(4)静脉注射100μg阿维鲁单抗-IR700并进行近红外光照射。与其他组相比,NIR-PIT治疗显著抑制了肿瘤生长(p<0.001),并且实现了显著延长生存期(与其他组相比,p<0.01)。总之,抗PD-L1抗体阿维鲁单抗适合作为NIR-PIT的APC。此外,阿维鲁单抗-IR700的NIR-PIT是治疗表达PD-L1肿瘤的一种有前景的候选方法,有望很快应用于人类。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e239/5341755/a6333754c306/oncotarget-08-8807-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验