化学
正电子发射断层摄影术
肽
粘蛋白
抗体
免疫疗法
癌症研究
蛋白酶
肿瘤微环境
临床前影像学
体内
Pet成像
分子成像
免疫球蛋白G
肿瘤细胞
分子生物学
碎片结晶区
免疫检查点
成像技术
细胞穿透肽
作者
Jiawen Huang,Jiale Xie,Junyu Bao,Kezhi Ding,Yuting Dai,Xiaochuan Zha,Chuan Chen,Wenhao Liu,Zonghua Luo
标识
DOI:10.1021/acs.bioconjchem.5c00504
摘要
T-cell immunoglobulin and mucin domain 3 (TIM-3), a critical immunosuppressive checkpoint receptor, regulates antitumor immunity within the tumor microenvironment (TME). Noninvasive quantification of TIM-3 expression could be helpful for guiding immunotherapy and monitoring treatment response. We developed 68 Ga-DOTA-D-P24, a novel D-configured peptide radiotracer designed for enhanced protease resistance and optimized TIM-3 targeting. Radiolabeling yielded high radiochemical purity (RCP) (>98%) and excellent in vitro / in vivo stability. Positron emission tomography (PET)/CT imaging across six tumor models demonstrated that 68 Ga-DOTA-D-P24 showed high specific uptake in MGC-803 gastric carcinoma. Comparative PET studies showed that the D -configured tracer exhibited 1.6-fold higher tumor uptake than that of 68 Ga-DOTA-L-P24. Furthermore, 68 Ga-DOTA-D-P24 successfully visualized the interleukin-15 (IL-15)-triggered elevation of TIM-3 expression in tumors, demonstrating its potential as a noninvasive tool for assessing target engagement and treatment response in TIM-3-associated malignancies.
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