Trachsel Eveline, Neri Dario
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology Zurich, Wolfgang-Pauli-Str.10, ETH Hönggerberg, HCI G396, CH-8093 Zürich, Switzerland.
Adv Drug Deliv Rev. 2006 Aug 7;58(5-6):735-54. doi: 10.1016/j.addr.2005.11.002. Epub 2006 May 20.
The endothelium is increasingly recognized as a target for biomedical intervention, not only for its accessibility to molecular agents coming from the blood-stream, but also for the active role played by endothelial cell proliferation to support diseases such as cancer, blinding ocular disorders and chronic inflammatory conditions. The notion that solid tumors cannot grow beyond a size of few millimeters without inducing the proliferation of new blood vessels has stimulated the search for mediators of angiogenesis and for inhibitors of this process, culminating in the approval of a humanized monoclonal antibody to VEGF-A for oncology applications. In parallel, researchers have begun to consider imaging and therapeutic strategies based on the selective delivery of bioactive agents to the new blood vessels, mediated by monoclonal antibody derivatives. Recently, the field of vascular targeting research has been extended to the investigation of molecular agents that may mediate endothelial cell transcytosis, in the hope to overcome this body barrier for drug delivery. This article reviews some of the most significant advances in these areas, and outlines future challenges and opportunities.
内皮细胞越来越被视为生物医学干预的靶点,这不仅是因为它易于接触来自血流的分子试剂,还因为内皮细胞增殖在支持癌症、致盲性眼部疾病和慢性炎症等疾病中发挥的积极作用。实体肿瘤如果不诱导新血管的增殖就无法生长到几毫米以上,这一观念激发了人们对血管生成介质和该过程抑制剂的寻找,最终促成了一种用于肿瘤学应用的人源化抗VEGF-A单克隆抗体的获批。与此同时,研究人员已经开始考虑基于单克隆抗体衍生物介导的生物活性剂向新血管的选择性递送的成像和治疗策略。最近,血管靶向研究领域已经扩展到对可能介导内皮细胞转胞吞作用的分子试剂的研究,以期克服这一药物递送的身体屏障。本文综述了这些领域的一些最重要进展,并概述了未来的挑战和机遇。