Langer Lee F, Clay Timothy M, Morse Michael A
Duke University Medical Center, Department of Surgery, Program in Molecular Therapeutics, Comprehensive Cancer Center, Durham, NC 27710, USA.
Expert Opin Biol Ther. 2007 Aug;7(8):1245-56. doi: 10.1517/14712598.7.8.1245.
Breaking immune tolerance against tumor self-antigens is presently an area of intense research in the design of cancer therapies. One possible method to enhance immune system activation against tumor antigens is by blocking the inhibitory co-stimulatory signals mediated by cytotoxic T lymphocyte antigen 4, (CTLA-4) expressed on activated T cells. The fully human monoclonal antibodies that are directed against human CTLA-4, ipilimumab (Medarex/Bristol-Myers Squibb) and CP-675,206 (Pfizer/Abgenix, now Amgen), have demonstrated activity against metastatic melanoma, hormone refractory prostate cancer and other malignancies. They have also uncovered unusual immune-related adverse events manifesting as self-limiting inflammatory reactions of the bowel, skin and pituitary. This article reviews preclinical development and data generated from Phase I, II and III studies with regard to the end points reported and immune-related adverse events.
打破针对肿瘤自身抗原的免疫耐受是目前癌症治疗设计中一个深入研究的领域。增强免疫系统针对肿瘤抗原激活的一种可能方法是阻断由活化T细胞上表达的细胞毒性T淋巴细胞抗原4(CTLA-4)介导的抑制性共刺激信号。针对人CTLA-4的全人源单克隆抗体,易普利姆玛(Medarex/百时美施贵宝)和CP-675,206(辉瑞/Abgenix,现安进),已显示出对转移性黑色素瘤、激素难治性前列腺癌和其他恶性肿瘤的活性。它们还揭示了不寻常的免疫相关不良事件,表现为肠道、皮肤和垂体的自限性炎症反应。本文回顾了临床前开发以及关于所报告终点和免疫相关不良事件的I、II和III期研究产生的数据。