Immuno-PET/CT Imaging of Trop2 with [18F]AlF-RESCA-T4 Differentiates Lung Cancer from Inflammation.

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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Abstract

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