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评估抗体 - PNA 缀合物作为基于抗体的 PNA 介导放射性核素前靶向的清除剂。

Evaluation of an antibody-PNA conjugate as a clearing agent for antibody-based PNA-mediated radionuclide pretargeting.

机构信息

Department of Protein Science, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, Stockholm, Sweden.

Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.

出版信息

Sci Rep. 2020 Nov 27;10(1):20777. doi: 10.1038/s41598-020-77523-y.

Abstract

Radionuclide molecular imaging of cancer-specific targets is a promising method to identify patients for targeted antibody therapy. Radiolabeled full-length antibodies however suffer from slow clearance, resulting in high background radiation. To overcome this problem, a pretargeting system based on complementary peptide nucleic acid (PNA) probes has been investigated. The pretargeting relies on sequential injections of primary, PNA-tagged antibody and secondary, radiolabeled PNA probe, which are separated in time, to allow for clearance of non-bound primary agent. We now suggest to include a clearing agent (CA), designed for removal of primary tumor-targeting agent from the blood. The CA is based on the antibody cetuximab, which was conjugated to PNA and lactosaminated by reductive amination to improve hepatic clearance. The CA was evaluated in combination with PNA-labelled trastuzumab, T-ZHP1, for radionuclide HER2 pretargeting. Biodistribution studies in normal mice demonstrated that the CA cleared ca. 7 times more rapidly from blood than unmodified cetuximab. Injection of the CA 6 h post injection of the radiolabeled primary agent [I]I-T-ZHP1 gave a moderate reduction of the radioactivity concentration in the blood after 1 h from 8.5 ± 1.8 to 6.0 ± 0.4%ID/g. These proof-of-principle results could guide future development of a more efficient CA.

摘要

癌症特异性靶点的放射性核素分子成像,是一种有前途的方法,可以识别接受靶向抗体治疗的患者。然而,放射性标记的全长抗体由于清除缓慢,导致背景辐射高。为了解决这个问题,人们研究了基于互补肽核酸(PNA)探针的前靶向系统。该前靶向系统依赖于初级 PNA 标记抗体和次级放射性标记 PNA 探针的顺序注射,这两种探针在时间上是分开的,以允许清除非结合的初级试剂。我们现在建议加入一种清除剂(CA),用于从血液中去除原发性肿瘤靶向剂。CA 基于抗体西妥昔单抗,通过还原胺化与 PNA 缀合,并通过乳糖胺化提高肝清除率。CA 与放射性标记的曲妥珠单抗(T-ZHP1)联合用于 HER2 放射性核素前靶向进行了评估。在正常小鼠中的生物分布研究表明,CA 从血液中的清除速度比未修饰的西妥昔单抗快约 7 倍。在注射放射性标记的初级试剂[I]I-T-ZHP1 后 6 小时注射 CA,在 1 小时后,血液中的放射性浓度从 8.5±1.8%ID/g 适度降低至 6.0±0.4%ID/g。这些原理验证结果可以为开发更有效的 CA 提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea26/7695838/e1792a06f23a/41598_2020_77523_Fig1_HTML.jpg

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