免疫疗法
适体
微泡
癌症免疫疗法
量子点
癌症
计算机科学
计算生物学
癌症生物标志物
免疫系统
纳米技术
癌症研究
材料科学
医学
生物
免疫学
小RNA
基因
分子生物学
内科学
生物化学
作者
Yupeng Zhang,Hua‐Jie Chen,Yusi Hu,Leping Lin,Haiyan Wen,Dai‐Wen Pang,Shiwu Zhang,Zhi‐Gang Wang,Shu‐Lin Liu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-01-25
卷期号:24 (5): 1816-1824
被引量:4
标识
DOI:10.1021/acs.nanolett.3c05060
摘要
Accurate quantification of exosomal PD-L1 protein in tumors is closely linked to the response to immunotherapy, but robust methods to achieve high-precision quantitative detection of PD-L1 expression on the surface of circulating exosomes are still lacking. In this work, we developed a signal amplification approach based on aptamer recognition and DNA scaffold hybridization-triggered assembly of quantum dot nanospheres, which enables bicolor phenotyping of exosomes to accurately screen for cancers and predict PD-L1-guided immunotherapeutic effects through machine learning. Through DNA-mediated assembly, we utilized two aptamers for simultaneous ultrasensitive detection of exosomal antigens, which have synergistic roles in tumor diagnosis and treatment prediction, and thus, we achieved better sample classification and prediction through machine-learning algorithms. With a drop of blood, we can distinguish between different cancer patients and healthy individuals and predict the outcome of immunotherapy. This approach provides valuable insights into the development of personalized diagnostics and precision medicine.
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