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跨越近红外一区到近红外二区的AUNP-12近红外荧光探针可实现肿瘤微环境中PD-1/PD-L1轴的检测。

AUNP-12 Near-Infrared Fluorescence Probes across NIR-I to NIR-II Enable Detection of PD-1/PD-L1 Axis in the Tumor Microenvironment.

作者信息

Zhang Xinyu, Wang Ping, Shi Guangyuan, Tang Chu, Xue Huadan

机构信息

Department of Radiology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, No. 1 Shuaifuyuan, Dongcheng District, Beijing 100730, China.

Department of Cardiology, The Second Medical Center & National Clinical Research Center for Geriatric Diseases, Chinese People's Liberation Army (PLA) General Hospital, 28 Fuxing Road, Haidian District, Beijing 100853, China.

出版信息

Bioconjug Chem. 2024 Jul 17;35(7):1064-1074. doi: 10.1021/acs.bioconjchem.4c00266. Epub 2024 Jul 9.

Abstract

The innovative PD-1/PD-L1 pathway strategy is gaining significant traction in cancer therapeutics. However, fluctuating response rates of 20-40% to PD-1/PD-L1 inhibitors, coupled with the risk of hyperprogression after immunotherapy, underscore the need for accurate patient selection and the identification of more beneficiaries. Molecular imaging, specifically near-infrared (NIR) fluorescence imaging, is a valuable alternative for real-time, noninvasive visualization of dynamic PD-L1 expression . This research introduces AUNP-12, a novel PD-L1-targeting peptide antagonist conjugated with Cy5.5 and CH1055 for first (NIR-I) and second near-infrared (NIR-II) imaging. These probes have proven to be effective in mapping PD-L1 expression across various mouse tumor models, offering insights into tumor-immune interactions. This study highlights the potential of AUNP-12-Cy5.5 and AUNP-12-CH1055 for guiding clinical immunotherapy through precise patient stratification and dynamic monitoring, supporting the shift toward molecular imaging for personalized cancer care.

摘要

创新的PD-1/PD-L1通路策略在癌症治疗中越来越受到关注。然而,PD-1/PD-L1抑制剂的有效率在20%-40%之间波动,加上免疫治疗后出现疾病快速进展的风险,凸显了准确选择患者和识别更多受益人群的必要性。分子成像,特别是近红外(NIR)荧光成像,是实时、无创可视化动态PD-L1表达的一种有价值的替代方法。本研究介绍了AUNP-12,一种新型的与Cy5.5和CH1055偶联的靶向PD-L1的肽拮抗剂,用于第一近红外(NIR-I)和第二近红外(NIR-II)成像。这些探针已被证明可有效绘制多种小鼠肿瘤模型中的PD-L1表达情况,为肿瘤-免疫相互作用提供见解。本研究强调了AUNP-12-Cy5.5和AUNP-12-CH1055通过精确的患者分层和动态监测指导临床免疫治疗的潜力,支持向分子成像的个性化癌症护理转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fec0/11261610/256181243361/bc4c00266_0004.jpg

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