State Key Laboratory of Nuclear Physics and Technology, School of Physics, Peking University, Beijing 100871, P. R. China.
Key Laboratory of Radiation Physics and Technology, Ministry of Education, Institute of Nuclear Science and Technology, Sichuan University, Chengdu 610064, P. R. China.
J Radiat Res. 2020 Sep 8;61(5):684-690. doi: 10.1093/jrr/rraa049.
Targeted alpha therapy (TAT) is a promising tumor therapy that can specifically transport α particle to the vicinity of tumor cells while the normal cells are only slightly irradiated. Mesothelin is a highly promising molecular signature for many types of solid tumors including malignant mesothelioma, pancreatic cancer, ovarian cancer and lung adenocarcinoma etc., while the expression in normal human tissues are limited, thus making mesothelin a promising antigen for TAT. Previously we developed a theoretical model that could predict and optimize in vitro screening of potential TAT drugs. The aim of the study is construction and preclinical evaluation of 211At labeled anti-mesothelin antibodies as potential TAT drugs. Mesothelin expression of two tumor cell lines were confirmed by flow cytometry, and their radiosensitivities were also evaluated. We used two kinds of anti-mesothelin antibodies, ET210-6 and ET210-28, to construct TAT drugs. Then, radiochemical purity, stability in vitro, affinity of the conjugates and mesothelin expression level were assessed. The specific killing of mesothelin-positive cancer cells treated by 211At-ET210-28 and 211At-ET210-6 were studied via Cell Counting Kit-8 assay and colony formation assay. 211At-ET210-28 and 211At-ET210-6 revealed excellent affinity and stability in both phosphate buffer saline and fetal bovine serum environment. Radiolabeled antibody conjugates bound specifically to mesothelin-positive cells in vitro. Both 211At-ET210-28 and 211At-ET210-6 could specifically kill mesothelin-positive cells with negligible damages to mesothelin-negative cells. Our findings provide initial proof-of-concept for the potential use of 211At labeled ET210-28/ET210-6 anti-mesothelin antibody in specific killings of mesothelin-positive tumor cells.
靶向 α 治疗(TAT)是一种很有前途的肿瘤治疗方法,它可以特异性地将 α 粒子输送到肿瘤细胞附近,而正常细胞只受到轻微的辐射。间皮素是许多类型的实体瘤(包括恶性间皮瘤、胰腺癌、卵巢癌和肺腺癌等)的一个非常有前途的分子标志物,而在正常人体组织中的表达有限,因此间皮素是 TAT 的一个很有前途的抗原。此前,我们开发了一种理论模型,可以预测和优化潜在 TAT 药物的体外筛选。本研究的目的是构建和临床前评估 211At 标记的抗间皮素抗体作为潜在 TAT 药物。通过流式细胞术证实了两种肿瘤细胞系的间皮素表达,并评估了它们的放射敏感性。我们使用两种抗间皮素抗体 ET210-6 和 ET210-28 来构建 TAT 药物。然后,评估了放射性化学纯度、体外稳定性、缀合物的亲和力和间皮素表达水平。通过细胞计数试剂盒-8 测定法和集落形成测定法研究了 211At-ET210-28 和 211At-ET210-6 处理的间皮素阳性癌细胞的特异性杀伤作用。211At-ET210-28 和 211At-ET210-6 在磷酸盐缓冲盐水和胎牛血清环境中均显示出优异的亲和力和稳定性。放射性标记的抗体缀合物在体外特异性结合间皮素阳性细胞。211At-ET210-28 和 211At-ET210-6 均可特异性杀伤间皮素阳性细胞,而对间皮素阴性细胞几乎没有损伤。我们的发现为 211At 标记的 ET210-28/ET210-6 抗间皮素抗体在间皮素阳性肿瘤细胞的特异性杀伤中的潜在应用提供了初步的概念验证。