间隙
癌症
生物
癌症治疗
癌症研究
计算生物学
癌症治疗
医学
遗传学
泌尿科
作者
Neema Ahishakiye Jumapili,Maida Živalj,Romina Mora Barthelmess,Geert Raes,Timo W. M. De Groof,Nick Devoogdt,Benoı̂t Stijlemans,Cécile Vincke,Jo A. Van Ginderachter
标识
DOI:10.1002/eji.202250024
摘要
Abstract mAbs have been instrumental for targeted cancer therapies. However, their relatively large size and physicochemical properties result in a heterogenous distribution in the tumor microenvironment, usually restricted to the first cell layers surrounding blood vessels, and a limited ability to penetrate the brain. Nanobodies are tenfold smaller, resulting in a deeper tumor penetration and the ability to reach cells in poorly perfused tumor areas. Nanobodies are rapidly cleared from the circulation, which generates a fast target‐to‐background contrast that is ideally suited for molecular imaging purposes but may be less optimal for therapy. To circumvent this problem, nanobodies have been formatted to noncovalently bind albumin, increasing their serum half‐life without majorly increasing their size. Finally, nanobodies have shown superior qualities to infiltrate brain tumors as compared to mAbs. In this review, we discuss why these features make nanobodies prime candidates for targeted therapy of cancer.
科研通智能强力驱动
Strongly Powered by AbleSci AI