Department of Radiology and Radiological Science, Johns Hopkins Medical Institutions, Baltimore, Maryland; and
Department of Radiology and Radiological Science, Johns Hopkins Medical Institutions, Baltimore, Maryland; and.
J Nucl Med. 2019 Mar;60(3):400-406. doi: 10.2967/jnumed.118.214403. Epub 2018 Sep 20.
5D3 is a new high-affinity murine monoclonal antibody specific for prostate-specific membrane antigen (PSMA). PSMA is a target for the imaging and therapy of prostate cancer. In-labeled antibodies have been used as surrogates for Lu/Y-labeled therapeutics. We characterized In-DOTA-5D3 by SPECT/CT imaging, tissue biodistribution studies, and dosimetry. Radiolabeling, stability, cell uptake, and internalization of In-DOTA-5D3 were performed by established techniques. Biodistribution and SPECT imaging were done on male nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice bearing human PSMA(+) PC3 PIP and PSMA(-) PC3 flu prostate cancer xenografts on the upper right and left flanks, respectively, at 2, 24, 48, 72, and 192 h after injection. Biodistribution was also evaluated in tumor-free, healthy male CD-1 mice. Blocking studies were performed by coinjection of a 10-fold and 50-fold excess of 5D3 followed by biodistribution at 24 h to determine PSMA binding specificity. The absorbed radiation doses were calculated on the basis of murine biodistribution data, which were translated to a human adult man using organ weights as implemented in OLINDA/EXM. In-DOTA-5D3 was synthesized with specific activity of approximately 2.24 ± 0.74 MBq/μg (60.54 ± 20 μCi/μg). Distribution of In-DOTA-5D3 in PSMA(+) PC3 PIP tumor peaked at 24 h after injection and remained high until 72 h. Uptake in normal tissues, including the blood, spleen, liver, heart, and lungs, was highest at 2 h after injection. Coinjection of In-DOTA-5D3 with a 10- and 50-fold excess of nonradiolabeled antibody significantly reduced PSMA(+) PC3 PIP tumor and salivary gland uptake at 24 h but did not reduce uptake in kidneys and lacrimal glands. Significant clearance of In-DOTA-5D3 from all organs occurred at 192 h. The highest radiation dose was received by the liver (0.5 mGy/MBq), followed by the spleen and kidneys. Absorbed radiation doses to the salivary and lacrimal glands and bone marrow were low. In-DOTA-5D3 is a new radiolabeled antibody for imaging and a surrogate for therapy of malignant tissues expressing PSMA.
5D3 是一种新型高亲和力的鼠单克隆抗体,特异性针对前列腺特异性膜抗原(PSMA)。PSMA 是前列腺癌成像和治疗的靶点。放射性标记的抗体已被用作 Lu/Y 标记治疗剂的替代物。我们通过 SPECT/CT 成像、组织分布研究和剂量学对 In-DOTA-5D3 进行了表征。通过既定技术进行了 In-DOTA-5D3 的放射性标记、稳定性、细胞摄取和内化。在注射后 2、24、48、72 和 192 小时,在分别在上右侧和左侧侧翼携带人 PSMA(+)PC3 PIP 和 PSMA(-)PC3 flu 前列腺癌异种移植的雄性非肥胖糖尿病/严重联合免疫缺陷(NOD/SCID)小鼠上进行了生物分布和 SPECT 成像。还在无肿瘤、健康的雄性 CD-1 小鼠中评估了生物分布。通过共注射 10 倍和 50 倍过量的 5D3 并在 24 小时进行生物分布来进行阻断研究,以确定 PSMA 结合特异性。根据鼠生物分布数据计算吸收的辐射剂量,然后使用器官重量将其转换为人类成年男子,OLINDA/EXM 中实现了这一点。In-DOTA-5D3 的比活度约为 2.24±0.74MBq/μg(60.54±20μCi/μg)。In-DOTA-5D3 在 PSMA(+)PC3 PIP 肿瘤中的分布在注射后 24 小时达到峰值,并在 72 小时内保持较高水平。在注射后 2 小时,包括血液、脾脏、肝脏、心脏和肺在内的正常组织中的摄取最高。在 24 小时时,与非放射性标记抗体共注射 10 倍和 50 倍过量的 In-DOTA-5D3 可显著减少 PSMA(+)PC3 PIP 肿瘤和唾液腺摄取,但不会减少肾脏和泪腺摄取。在 192 小时时,In-DOTA-5D3 从所有器官中的清除率显著增加。肝脏(0.5 mGy/MBq)接收到的辐射剂量最高,其次是脾脏和肾脏。唾液腺和泪腺以及骨髓的吸收辐射剂量较低。In-DOTA-5D3 是一种用于成像的新型放射性标记抗体,也是表达 PSMA 的恶性组织的治疗替代物。