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用于免疫正电子发射断层扫描成像的新型锆标记靶向B细胞成熟抗原抗体的研发及临床前验证:在多发性骨髓瘤模型中的应用及首次非人灵长类动物实验

Development and Preclinical Validation of a Novel Zr-Labeled BCMA-Targeting Antibody for ImmunoPET Imaging: Application in Multiple Myeloma Models and First-In-Nonhuman-Primates.

作者信息

Wang Tianyao, Yang Qi, Huang Wenpeng, Sun Xinyao, Lei Youlan, Xu Hui, Song Lele, Duan Xiaojiang, Liu Futao, Wang Wenzhi, Bao Zheng, Gao Jinquan, Wang Feng, Kang Lei

机构信息

Department of Nuclear Medicine, Peking University First Hospital, Beijing 100034, China.

Key Laboratory of Carcinogenesis and Translational Research, (Ministry of Education/Beijing), Key Laboratory for Research and Evaluation of Radiopharmaceuticals (National Medical Products Administration), Department of Nuclear Medicine, Peking University Cancer Hospital & Institute, Beijing 100142, China.

出版信息

J Med Chem. 2025 Jul 24;68(14):14843-14858. doi: 10.1021/acs.jmedchem.5c01010. Epub 2025 Jun 25.

Abstract

B-cell maturation antigen (BCMA) is a clinically validated biomarker and therapeutic target in multiple myeloma (MM). Here, we report the design, synthesis, and preclinical evaluation of an immunoPET probe, [Zr]Zr-DFO-PFBH0L0, derived from a novel humanized anti-BCMA monoclonal antibody. The antibody was conjugated with deferoxamine (DFO) and radiolabeled with zirconium-89 (Zr), yielding a probe with excellent in vitro stability. The tracer retained high binding affinity and demonstrated specific binding to BCMA-positive MM cell lines. In vivo PET imaging and biodistribution studies demonstrated significantly higher tumor uptake in H929-bearing BCMA xenografts (10.04 ± 1.04% ID/g) and a tumor-to-blood ratio exceeding 88, outperforming all controls. Notably, this study presents the first BCMA-targeted PET/CT imaging in nonhuman primates (rhesus macaques), revealing favorable pharmacokinetics, biodistribution, and metabolic stability - underscoring its translational potential for clinical immunoPET imaging and therapeutic monitoring. These results establish [Zr]Zr-DFO-PFBH0L0 as a promising immunoPET imaging agent for noninvasive, whole-body evaluation of BCMA-expressing malignancies.

摘要

B细胞成熟抗原(BCMA)是多发性骨髓瘤(MM)中经过临床验证的生物标志物和治疗靶点。在此,我们报告了一种免疫正电子发射断层扫描(immunoPET)探针[Zr]Zr-DFO-PFBH0L0的设计、合成及临床前评估,该探针源自一种新型人源化抗BCMA单克隆抗体。该抗体与去铁胺(DFO)偶联,并使用锆-89(Zr)进行放射性标记,得到一种具有出色体外稳定性的探针。该示踪剂保留了高结合亲和力,并证明与BCMA阳性的MM细胞系具有特异性结合。体内PET成像和生物分布研究表明,在携带H929的BCMA异种移植瘤中肿瘤摄取显著更高(10.04±1.04% ID/g),肿瘤与血液的比率超过88,优于所有对照。值得注意的是,本研究展示了在非人类灵长类动物(恒河猴)中首次进行的靶向BCMA的PET/CT成像,揭示了良好的药代动力学、生物分布和代谢稳定性——突出了其在临床免疫PET成像和治疗监测方面的转化潜力。这些结果确立了[Zr]Zr-DFO-PFBH0L0作为一种有前景的免疫PET成像剂,可用于对表达BCMA的恶性肿瘤进行无创全身评估。

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