体内分布
化学
体内
多发性骨髓瘤
单克隆抗体
Spect成像
药代动力学
显像剂
抗体
癌症研究
核医学
体外
药理学
免疫学
医学
生物化学
生物技术
生物
作者
Tianyao Wang,Qi Yang,Wenpeng Huang,Xinyao Sun,Youlan Lei,Hui Xu,Lele Song,Xiaojiang Duan,Futao Liu,Wenzhi Wang,Zheng Bao,Jie Gao,Feng Wang,Lei Kang
标识
DOI:10.1021/acs.jmedchem.5c01010
摘要
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, [89Zr]Zr-DFO-PFBH0L0, derived from a novel humanized anti-BCMA monoclonal antibody. The antibody was conjugated with deferoxamine (DFO) and radiolabeled with zirconium-89 (89Zr), 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 [89Zr]Zr-DFO-PFBH0L0 as a promising immunoPET imaging agent for noninvasive, whole-body evaluation of BCMA-expressing malignancies.
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