Providence Cancer Research Center, Earle A. Chiles Research Institute, Providence Portland Medical Center, Portland, OR 97213, USA.
Immunol Rev. 2011 Nov;244(1):218-31. doi: 10.1111/j.1600-065X.2011.01069.x.
OX40 (CD134) is a tumor necrosis factor (TNF) receptor expressed primarily on activated CD4(+) and CD8(+) T cells and transmits a potent costimulatory signal when engaged. OX40 is transiently expressed after T-cell receptor engagement and is upregulated on the most recently antigen-activated T cells within inflammatory lesions (e.g. sites of autoimmune destruction and on tumor-infiltrating lymphocytes). Hence, it is an attractive target to modulate immune responses: OX40 blocking agents to inhibit undesirable inflammation or OX40 agonists to enhance immune responses. In regards to this review, OX40 agonists enhance anti-tumor immunity, which leads to therapeutic effects in mouse tumor models. A team of laboratory and clinical scientists at the Providence Cancer Center has collaborated to bring the preclinical observations in cancer models from the bench to the bedside. This review describes the journey from in vitro experiments through preclinical mouse models to the successful translation of the first OX40 agonist to the clinic for the treatment of patients with cancer.
OX40(CD134)是一种肿瘤坏死因子(TNF)受体,主要表达于活化的 CD4(+)和 CD8(+)T 细胞上,当与之结合时会传递一种强烈的共刺激信号。OX40 在 T 细胞受体结合后短暂表达,并在上皮内炎症病灶(如自身免疫破坏部位和肿瘤浸润淋巴细胞)中最近被抗原激活的 T 细胞上上调。因此,它是调节免疫反应的一个有吸引力的靶点:OX40 阻断剂抑制不必要的炎症,或 OX40 激动剂增强免疫反应。关于这篇综述,OX40 激动剂增强了抗肿瘤免疫,从而在小鼠肿瘤模型中产生了治疗效果。普罗维登斯癌症中心的一组实验室和临床科学家合作,将癌症模型中的临床前观察结果从实验室转化到床边。这篇综述描述了从体外实验到临床前小鼠模型,再到成功将第一种 OX40 激动剂转化为治疗癌症患者的临床应用的历程。