用[18F]AlF-RESCA-T4对Trop2进行免疫PET/CT成像,可区分肺癌和炎症。

Wei Huang, Min Cao, Yanfei Wu, You Zhang, Shuxian An, Xinbing Pan, Xinyuan Zhou, Hongda Shao, Yihui Guan, Gang Huang, Fabrizia Gelardi, Arturo Chiti, Fang Xie, Jianjun Liu, Weijun Wei
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引用次数: 0

摘要

免疫-PET/CT成像是分子成像的一个分支,可以无创、特异性地观察全身生物标记物的表达。滋养层细胞表面抗原2(Trop2)是一种泛癌症生物标志物,通过多种信号通路在肿瘤发生过程中发挥关键作用。该研究旨在开发新型 Trop2 单域抗体(sdAb)示踪剂并将其应用于临床。研究方法在中国仓鼠卵巢细胞中重组表达两种 sdAb(即 His 标记的 T4 和无 His 标记的 RT4)。纯度和结合动力学是通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳、高效液相色谱和表面等离子体共振检测确定的。应用 AlF 限制复合剂(RESCA)方法开发了 18F 标记的 sdAb 示踪剂([18F]AlF-RESCA-T4 和 [18F]AlF-RESCA-RT4),随后在肿瘤小鼠上进行了全面的临床前成像和阻断研究,并进行了试点临床试验,评估 [18F]AlF-RESCA-T4 免疫 PET/CT 的临床成像安全性和可行性。研究结果[18F]AlF-RESCA-T4和[18F]AlF-RESCA-RT4具有很高的放射化学纯度。T3M-4肿瘤模型的临床前成像显示,[18F]AlF-RESCA-T4(11.13 ± 1.53,n = 4)和[18F]AlF-RESCA-RT4(8.83 ± 1.22,n = 4)的摄取量(注射剂量/克百分比)显著增加,在阻断研究中,联合注射未标记的T4和RT4可显著减少摄取量。去除 His 标记的策略进一步优化了探针的体内药代动力学,减少了肾脏放射性累积,同时也没有显著降低肿瘤摄取。在一项试点临床试验中,[18F]AlF-RESCA-T4 免疫 PET/CT 在注释 Trop2 表达和区分肿瘤与结核等炎症性疾病方面显示出良好的功效。结论[18F]AlF-RESCA-T4和[18F]AlF-RESCA-RT4可特异性标记Trop2的表达。临床[18F]AlF-RESCA-T4免疫PET/CT成像可筛选Trop2靶向疗法患者,并区分肺部炎症和癌症。
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Immuno-PET/CT Imaging of Trop2 with [18F]AlF-RESCA-T4 Differentiates Lung Cancer from Inflammation.

Immuno-PET/CT imaging, a branch of molecular imaging, can noninvasively and specifically visualize biomarker expression across the body. Trophoblast cell surface antigen 2 (Trop2) is a pan-cancer biomarker and plays a crucial role in tumorigenesis through multiple signaling pathways. The study aims to develop and translate novel Trop2 single-domain antibody (sdAb) tracers for clinical use. Methods: Two sdAbs (i.e., His-tagged T4 and His-tag-free RT4) are recombinantly expressed in Chinese hamster ovary cells. The purities and binding kinetics are determined by sodium dodecyl sulfate polyacrylamide gel electrophoresis, high-performance liquid chromatography, and surface plasmon resonance assays. The AlF restrained complexing agent (RESCA) method is applied to develop 18F-labeled sdAb tracers ([18F]AlF-RESCA-T4 and [18F]AlF-RESCA-RT4), followed by thorough preclinical imaging and blocking studies on tumor-bearing mice and a pilot clinical trial evaluating the clinical imaging safety and feasibility of [18F]AlF-RESCA-T4 immuno-PET/CT. Results: [18F]AlF-RESCA-T4 and [18F]AlF-RESCA-RT4 possess high radiochemical purities. Preclinical imaging in the T3M-4 tumor model revealed prominent uptake (percentage injected dose/g) of [18F]AlF-RESCA-T4 (11.13 ± 1.53, n = 4) and [18F]AlF-RESCA-RT4 (8.83 ± 1.22, n = 4), which were significantly reduced by coinjection of unlabeled T4 and RT4 in blocking studies. The His-tag removal strategy further optimized the probe's in vivo pharmacokinetics and reduced renal radioactivity accumulation without significantly decreasing tumor uptake. In a pilot clinical trial, [18F]AlF-RESCA-T4 immuno-PET/CT showed promising potency in annotating Trop2 expression and differentiating tumors from inflammatory diseases such as tuberculosis. Conclusion: [18F]AlF-RESCA-T4 and [18F]AlF-RESCA-RT4 can specifically annotate Trop2 expression. Clinical [18F]AlF-RESCA-T4 immuno-PET/CT imaging can screen patients for Trop2-targeted therapies and differentiate lung inflammation from cancer.

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