INSERM, U848; Villejuif, France ; Institut Gustave Roussy; Villejuif, France ; Université Paris-Sud/Paris XI; Le Kremlin-Bicêtre, France.
Oncoimmunology. 2012 Jan 1;1(1):28-37. doi: 10.4161/onci.1.1.17938.
Since the advent of hybridoma technology, dating back to 1975, monoclonal antibodies have become an irreplaceable diagnostic and therapeutic tool for a wide array of human diseases. During the last 15 years, several monoclonal antibodies (mAbs) have been approved by FDA for cancer therapy. These mAbs are designed to (1) activate the immune system against tumor cells, (2) inhibit cancer cell-intrinsic signaling pathways, (3) bring toxins in the close proximity of cancer cells, or (4) interfere with the tumor-stroma interaction. More recently, major efforts have been made for the development of immunostimulatory mAbs that either enhance cancer-directed immune responses or limit tumor- (or therapy-) driven immunosuppression. Some of these antibodies, which are thought to facilitate tumor eradication by initiating or sustaining a tumor-specific immune response, have already entered clinical trials. In this Trial Watch, we will review and discuss the clinical progress of the most important mAbs that are have entered clinical trials after January 2008.
自 1975 年杂交瘤技术问世以来,单克隆抗体已成为治疗多种人类疾病不可或缺的诊断和治疗工具。在过去的 15 年中,FDA 已经批准了几种单克隆抗体(mAbs)用于癌症治疗。这些 mAbs 的设计目的是:(1)激活免疫系统对抗肿瘤细胞,(2)抑制癌细胞内在的信号通路,(3)使毒素接近癌细胞,或(4)干扰肿瘤-基质相互作用。最近,人们为开发免疫刺激 mAbs 做出了巨大努力,这些 mAbs 可以增强针对癌症的免疫反应或限制肿瘤(或治疗)驱动的免疫抑制。其中一些抗体被认为通过启动或维持肿瘤特异性免疫反应来促进肿瘤的清除,它们已经进入临床试验。在本次临床试验观察中,我们将回顾和讨论自 2008 年 1 月以来进入临床试验的最重要的 mAbs 的临床进展。