封锁
支柱
癌症研究
肿瘤科
癌症
免疫疗法
医学
癌症免疫疗法
免疫检查点
内科学
结构工程
工程类
受体
作者
Rinat Meir,Katerina Shamalov,Tamar Sadan,Menachem Motiei,Gur Yaari,Cyrille J. Cohen,Rachela Popovtzer
出处
期刊:ACS Nano
[American Chemical Society]
日期:2017-10-20
卷期号:11 (11): 11127-11134
被引量:104
标识
DOI:10.1021/acsnano.7b05299
摘要
Cancer immunotherapy has made enormous progress in offering safer and more effective treatments for the disease. Specifically, programmed death ligand 1 antibody (αPDL1), designed to perform immune checkpoint blockade (ICB), is now considered a pillar in cancer immunotherapy. However, due to the complexity and heterogeneity of tumors, as well as the diversity in patient response, ICB therapy only has a 30% success rate, at most; moreover, the efficacy of ICB can be evaluated only two months after start of treatment. Therefore, early identification of potential responders and nonresponders to therapy, using noninvasive means, is crucial for improving treatment decisions. Here, we report a straightforward approach for fast, image-guided prediction of therapeutic response to ICB. In a colon cancer mouse model, we demonstrate that the combination of computed tomography imaging and gold nanoparticles conjugated to αPDL1 allowed prediction of therapeutic response, as early as 48 h after treatment. This was achieved by noninvasive measurement of nanoparticle accumulation levels within the tumors. Moreover, we show that the nanoparticles efficiently prevented tumor growth with only a fifth of the standard dosage of clinical care. This technology may be developed into a powerful tool for early and noninvasive patient stratification as responders or nonresponders.
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