Smaglo Brandon G, Aldeghaither Dalal, Weiner Louis M
Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, 3970 Reservoir Road NW, Washington, DC 20057, USA.
Nat Rev Clin Oncol. 2014 Nov;11(11):637-48. doi: 10.1038/nrclinonc.2014.159. Epub 2014 Sep 30.
Immunoconjugates are specific, highly effective, minimally toxic anticancer therapies that are beginning to show promise in the clinic. Immunoconjugates consist of three separate components: an antibody that binds to a cancer cell antigen with high specificity, an effector molecule that has a high capacity to kill the cancer cell, and a linker that will ensure the effector does not separate from the antibody during transit and will reliably release the effector to the cancer cell or tumour stroma. The high affinity antibody-antigen interaction allows specific and selective delivery of a range of effectors, including pharmacologic agents, radioisotopes, and toxins, to cancer cells. Some anticancer molecules are not well tolerated when administered systemically owing to unacceptable toxicity to the host. However, this limitation can be overcome through the linking of such cytotoxins to specific antibodies, which mask the toxic effects of the drug until it reaches its target. Conversely, many unconjugated antibodies are highly specific for a cancer target, but have low therapeutic potential and can be repurposed as delivery vehicles for highly potent effectors. In this Review, we summarize the successes and shortcomings of immunoconjugates, and discuss the future potential for the development of these therapies.
免疫偶联物是一种特异性强、疗效高、毒性低的抗癌疗法,已开始在临床上显示出应用前景。免疫偶联物由三个独立的成分组成:一种能高度特异性结合癌细胞抗原的抗体、一种具有高杀伤癌细胞能力的效应分子,以及一种连接子,该连接子可确保效应分子在转运过程中不与抗体分离,并能可靠地将效应分子释放到癌细胞或肿瘤基质中。高亲和力的抗体 - 抗原相互作用使得一系列效应分子(包括药物、放射性同位素和毒素)能够特异性、选择性地递送至癌细胞。一些抗癌分子由于对宿主具有不可接受的毒性,全身给药时耐受性不佳。然而,通过将此类细胞毒素与特异性抗体连接,可以克服这一限制,抗体可掩盖药物的毒性作用,直至其到达靶点。相反,许多未偶联的抗体对癌症靶点具有高度特异性,但治疗潜力较低,可重新用作高效应分子的递送载体。在本综述中,我们总结了免疫偶联物的成功与不足,并讨论了这些疗法未来的发展潜力。