Altai Mohamed, Membreno Rosemery, Cook Brendon, Tolmachev Vladimir, Zeglis Brian M
Department of Immunology, Genetics, and Pathology, Uppsala University, Uppsala, Sweden.
Department of Chemistry, Hunter College of the City University of New York, New York, New York.
J Nucl Med. 2017 Oct;58(10):1553-1559. doi: 10.2967/jnumed.117.189944. Epub 2017 Jul 7.
In vivo pretargeting stands as a promising approach to harnessing the exquisite tumor-targeting properties of antibodies for nuclear imaging and therapy while simultaneously skirting their pharmacokinetic limitations. The core premise of pretargeting lies in administering the targeting vector and radioisotope separately and having the 2 components combine within the body. In this manner, pretargeting strategies decrease the circulation time of the radioactivity, reduce the uptake of the radionuclide in healthy nontarget tissues, and facilitate the use of short-lived radionuclides that would otherwise be incompatible with antibody-based vectors. In this short review, we seek to provide a brief yet informative survey of the 4 preeminent mechanistic approaches to pretargeting, strategies predicated on streptavidin and biotin, bispecific antibodies, complementary oligonucleotides, and bioorthogonal click chemistry.
体内预靶向是一种很有前景的方法,可利用抗体出色的肿瘤靶向特性进行核成像和治疗,同时规避其药代动力学限制。预靶向的核心前提是分别给予靶向载体和放射性同位素,使这两种成分在体内结合。通过这种方式,预靶向策略可缩短放射性物质的循环时间,减少放射性核素在健康非靶组织中的摄取,并便于使用否则与基于抗体的载体不兼容的短寿命放射性核素。在这篇简短的综述中,我们旨在对预靶向的4种卓越机制方法进行简要而详实的概述,这些策略基于链霉亲和素和生物素、双特异性抗体、互补寡核苷酸以及生物正交点击化学。