Hetzel C, Bachran C, Tur M K, Fuchs H, Stöcker M
Fraunhofer IME, Department of Pharmaceutical Product Development, Forckenbeckstr. 6, 52074 AACHEN, Germany.
Curr Pharm Des. 2009;15(23):2700-11. doi: 10.2174/138161209788923930.
Immunotoxins (ITs) are protein-based drugs combining a target-specific binding domain (usually derived from an antibody) and a cytotoxic domain to kill target cells. They are among the most promising new therapeutic tools to fight cancer, and several clinical trials have been completed with encouraging results. Although the targeted elimination of malignant cells is an elegant concept, there are numerous practical challenges that limit the clinical use of ITs, including inefficient cellular uptake, low cytotoxicity and off-target effects. Here we present some of the strategies that have been developed to improve the efficacy of ITs, particularly those involving the incorporation of functional peptide sequences into recombinant ITs to improve target binding, modify plasma half life and distribution, boost tumor penetration, enhance cellular uptake and increase cytotoxic efficiency.
免疫毒素(ITs)是一种基于蛋白质的药物,它结合了一个靶向特异性结合结构域(通常来源于抗体)和一个细胞毒性结构域以杀死靶细胞。它们是对抗癌症最有前景的新型治疗工具之一,并且已经完成了多项临床试验,结果令人鼓舞。尽管靶向清除恶性细胞是一个精妙的概念,但仍有许多实际挑战限制了免疫毒素的临床应用,包括细胞摄取效率低下、细胞毒性低和脱靶效应。在此,我们介绍了一些已开发出的提高免疫毒素疗效的策略,特别是那些涉及将功能性肽序列整合到重组免疫毒素中以改善靶标结合、改变血浆半衰期和分布、增强肿瘤穿透性、提高细胞摄取并增加细胞毒性效率的策略。