探测claud18.2的68Ga/18F/ 64cu标记纳米体示踪剂的研制与比较

IF 5.3 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Molecular Therapy Oncolytics Pub Date : 2022-12-15 DOI:10.1016/j.omto.2022.11.003
Weijun Wei, Di Zhang, You Zhang, Lianghua Li, Yuchen Jin, Shuxian An, Chun Lv, Haitao Zhao, Cheng Wang, Yanshan Huang, Jiali Dong, Gang Huang, Jianjun Liu
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引用次数: 5

摘要

Claudin 18.2 (CLDN18.2)是一个新兴的胃癌治疗靶点。我们的目标是开发示踪剂来成像CLDN18.2的表达。制备了靶向CLDN18.2的人源化纳米体(克隆hu19V3),并用68Ga、64Cu和18F标记。该示踪剂在两种不同小鼠类型(裸小鼠和Balb/c小鼠)和两种不同细胞系(CHO-CLDN18.2和CT26-CLDN18.2)建立的皮下和转移模型中进行了研究。进一步建立胃癌患者源性异种移植瘤(PDX)模型进行验证实验。开发了三种新型cldn18.2靶向示踪剂(即[68Ga]Ga-NOTA-hu19V3, [64Cu]Cu-NOTA-hu19V3和[18F]F-hu19V3),具有良好的放射化学产率和优异的放射化学纯度。[68Ga]Ga-NOTA-hu19V3免疫正电子发射断层扫描(immunoPET)快速描绘皮下CHO-CLDN18.2病变和CT26-CLDN18.2肿瘤,并在自然表达CLDN18.2的PDX模型中显示出良好的诊断价值。[68Ga]Ga-NOTA-hu19V3肾脏堆积较多,[64Cu]Cu-NOTA-hu19V3肾脏堆积较少,后期图像对比度提高。此外,[18F]F-hu19V3在温和条件下通过点击化学反应产生,并在肺部精确播散CHO-CLDN18.2病变。此外,兴趣区分析、生物分布研究和组织病理学染色结果与体内成像结果具有良好的相关性。综上所述,三种示踪剂的免疫pet成像可以可靠地显示CLDN18.2的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Development and comparison of 68Ga/18F/64Cu-labeled nanobody tracers probing Claudin18.2.

Claudin 18.2 (CLDN18.2) is an emerging target for the treatment of gastric cancers. We aim to develop tracers to image the expression of CLDN18.2. A humanized nanobody targeting CLDN18.2 (clone hu19V3) was produced and labeled with 68Ga, 64Cu, and 18F. The tracers were investigated in subcutaneous and metastatic models established using two different mouse types (nude and Balb/c mice) and two different cell lines (CHO-CLDN18.2 and CT26-CLDN18.2). Gastric cancer patient-derived xenograft (PDX) models were further established for validation experiments. Three novel CLDN18.2-targeted tracers (i.e., [68Ga]Ga-NOTA-hu19V3, [64Cu]Cu-NOTA-hu19V3, and [18F]F-hu19V3) were developed with good radiochemical yields and excellent radiochemical purities. [68Ga]Ga-NOTA-hu19V3 immuno-positron emission tomography (immunoPET) rapidly delineated subcutaneous CHO-CLDN18.2 lesions and CT26-CLDN18.2 tumors, as well as showing excellent diagnostic value in PDX models naturally expressing CLDN18.2. While [68Ga]Ga-NOTA-hu19V3 had high kidney accumulation, [64Cu]Cu-NOTA-hu19V3 showed reduced kidney accumulation and improved image contrast at late time points. Moreover, [18F]F-hu19V3 was developed via click chemistry reaction under mild conditions and precisely disseminated CHO-CLDN18.2 lesions in the lungs. Furthermore, region of interest analysis, biodistribution study, and histopathological staining results correlated well with the in vivo imaging results. Taken together, immunoPET imaging with the three tracers can reliably visualize CLDN18.2 expression.

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来源期刊
Molecular Therapy Oncolytics
Molecular Therapy Oncolytics Medicine-Oncology
CiteScore
10.90
自引率
3.50%
发文量
152
审稿时长
6 weeks
期刊介绍: Molecular Therapy — Oncolytics is an international, online-only, open access journal focusing on the development and clinical testing of viral, cellular, and other biological therapies targeting cancer.
期刊最新文献
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