[64Cu]Cu-NOTA-TSHR-Ab在甲状腺癌中促甲状腺激素受体表达的临床前免疫pet成像

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Wenhui Fu, Ephraim E. Parent, Justyna J. Gleba, Joshua A. Knight, Otto Muzik, John A. Copland III* and Hancheng Cai*, 
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Human anti-TSHR recombinant antibody K1-70 (TSHR-Ab) was labeled with copper-64, yielding [<sup>64</sup>Cu]Cu-NOTA-TSHR-Ab with a radiochemical yield of 46.89 ± 3.74%, radiochemical purity of 98.77 ± 0.89%, and specific activity &gt;212 GBq/μmol (<i>n</i> = 5). <i>In vitro</i> studies on TSHR-positive (THJ529T<i><sup>TSHR+</sup></i>) and wild-type (THJ529T<i><sup>WT</sup></i>) cells demonstrated the radiotracer’s high specificity and nanomolar binding affinity for THJ529T<i><sup>TSHR+</sup></i> cells, with a dissociation constant (<i>K</i><sub>d</sub>) of 4.74 nM and an inhibition constant (<i>K</i><sub>i</sub>) of 0.92 nM. 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引用次数: 0

摘要

晚期甲状腺癌具有侵袭性,目前的治疗标准难以治疗。促甲状腺激素受体(TSHR)在甲状腺癌中高表达,很少在甲状腺外表达,使其成为发展晚期甲状腺癌影像学和治疗放射治疗的可行靶点。本研究报道了一种64cu标记的人抗体的放射合成和临床前评价,用于晚期甲状腺癌小鼠模型中TSHR表达的正电子发射断层扫描(PET)成像。用铜-64标记人抗tshr重组抗体K1-70 (TSHR-Ab),得到[64Cu]Cu-NOTA-TSHR-Ab,放射化学产率为46.89±3.74%,放射化学纯度为98.77±0.89%,比活性为bb0 212 GBq/μmol (n = 5)。对tshr阳性细胞(THJ529TTSHR+)和野生型细胞(THJ529TWT)的体外研究表明,该放射性示踪剂对THJ529TTSHR+细胞具有高特异性和纳米摩尔结合亲和力,解离常数(Kd)为4.74 nM,抑制常数(Ki)为0.92 nM。在注射后多个时间点(1、2、4、18、24和48 h)对双侧侧腹肿瘤(THJ529TWT和THJ529TTSHR+)小鼠的免疫pet成像显示,tshr阳性甲状腺肿瘤的肿瘤靶向性快,摄取高(18、24和48 h的SUVmax分别为3.63±0.42、3.82±0.44和4.09±0.56)。不同剂量的未标记TSHR-Ab(0、25、50、100 μg)共注射研究表明,共注射显著降低了背景信号,特别是在脾脏、肝脏和骨骼中,25 μg的剂量有效降低了脱靶信号,而不影响肿瘤的摄取。生物分布和免疫组织化学分析支持这些免疫pet成像结果。此外,与传统[18F]FDG PET成像的对比研究表明,[64Cu]Cu-NOTA-TSHR在肿瘤检测方面优于[18F]FDG。综上所述,[64Cu]Cu-NOTA-TSHR-Ab是一种很有前景的tshr阳性晚期甲状腺癌PET显像示踪剂,具有指导和监测tshr靶向治疗的潜力。[64Cu]Cu-NOTA-TSHR-Ab的进一步临床评价可为患者分层和优化抗tshr治疗提供有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Preclinical ImmunoPET Imaging of Thyroid-Stimulating Hormone Receptor Expression in Thyroid Cancer using [64Cu]Cu-NOTA-TSHR-Ab

Preclinical ImmunoPET Imaging of Thyroid-Stimulating Hormone Receptor Expression in Thyroid Cancer using [64Cu]Cu-NOTA-TSHR-Ab

Advanced thyroid cancers are aggressive and often refractory to the current standard of care. The thyroid-stimulating hormone receptor (TSHR) is highly expressed in thyroid cancers and rarely expressed outside the thyroid, making it a viable target for developing radiotheranostics for imaging and therapy of advanced thyroid cancer. This study reports the radiosynthesis and preclinical evaluation of a 64Cu-labeled human antibody for positron emission tomography (PET) imaging of TSHR expression in advanced thyroid cancer mouse models. Human anti-TSHR recombinant antibody K1-70 (TSHR-Ab) was labeled with copper-64, yielding [64Cu]Cu-NOTA-TSHR-Ab with a radiochemical yield of 46.89 ± 3.74%, radiochemical purity of 98.77 ± 0.89%, and specific activity >212 GBq/μmol (n = 5). In vitro studies on TSHR-positive (THJ529TTSHR+) and wild-type (THJ529TWT) cells demonstrated the radiotracer’s high specificity and nanomolar binding affinity for THJ529TTSHR+ cells, with a dissociation constant (Kd) of 4.74 nM and an inhibition constant (Ki) of 0.92 nM. ImmunoPET imaging in mice bearing dual-flank tumors (THJ529TWT and THJ529TTSHR+) at multiple time points (1, 2, 4, 18, 24, and 48 h) postinjection (p.i.) revealed rapid tumor targeting and high uptake in TSHR-positive thyroid tumors (SUVmax: 3.63 ± 0.42, 3.82 ± 0.44, and 4.09 ± 0.56 at 18, 24, and 48 h p.i., respectively). Co-injection studies with varying doses of unlabeled TSHR-Ab (0, 25, 50, 100 μg) demonstrated that the coinjection significantly reduced background signals, especially in the spleen, liver, and bone, with a dose of 25 μg effectively reducing off-target signals without affecting tumor uptake. Biodistribution and immunohistochemistry analyses supported these immunoPET imaging results. Furthermore, a comparison study with traditional [18F]FDG PET imaging showed that [64Cu]Cu-NOTA-TSHR outperformed [18F]FDG in tumor detection. In conclusion, [64Cu]Cu-NOTA-TSHR-Ab is a promising radiotracer for PET imaging of TSHR-positive advanced thyroid cancers, with the potential to guide and monitor TSHR-targeted therapies. Further clinical evaluation of [64Cu]Cu-NOTA-TSHR-Ab could provide valuable insights for patient stratification and optimization of anti-TSHR treatments.

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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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