免疫疗法
癌症研究
黑色素瘤
生物标志物
细胞外小泡
癌症免疫疗法
癌症
医学
生物
细胞生物学
内科学
生物化学
作者
Junli Zhang,Mengting Guan,Min Lv,Yingying Liu,Hongling Zhang,Zhenzhong Zhang,Kaixiang Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-10-11
卷期号:17 (20): 20120-20134
被引量:4
标识
DOI:10.1021/acsnano.3c05799
摘要
Programmed death-ligand 1 (PD-L1) on tumor-derived small extracellular vesicles (EVs) is a biomarker for prediction of the immunotherapy response. However, conventional bulk measurement can hardly analyze the expression of PD-L1 on individual tumor-derived EVs. Herein, a method for localized imaging of tumor-derived individual EVs PD-L1 (LITIE) is developed. In this assay, EVs in plasma were directly captured on a biochip. Then the liposome-mediated membrane fusion strategy was used to image miR-21 in EVs to discriminate miR-21-positive EVs from the whole EVs populations. Subsequently, the primer exchange reaction (PER) is applied to generate localized and amplified fluorescent signals for imaging PD-L1 on identified tumor-derived EVs. When applied in clinical sample tests, the LITIE assay could effectively distinguish breast cancer patients from healthy donors or patients with benign tumors. Interestingly, in a mice melanoma model, the LITIE assay showed the ability to predict immunotherapy response even before drug treatment. Thus, we think the strategy of measuring individual tumor-derived EVs PD-L1 could serve as an alternative way for screening clinical responders suitable for immunotherapy.
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