Melero Ignacio, Murillo Oihana, Dubrot Juan, Hervás-Stubbs Sandra, Perez-Gracia José L
Center for Applied Medical Research, Universidad de Navarra, Avenida de Pio XII, 55. 31008 Pamplona, Spain.
Trends Pharmacol Sci. 2008 Aug;29(8):383-90. doi: 10.1016/j.tips.2008.05.005. Epub 2008 Jul 1.
CD137 (also known as 4-1BB) is a surface co-stimulatory glycoprotein originally described as present on activated T lymphocytes. Artificial stimulation of this molecule with monoclonal antibodies or other agonist moieties therapeutically augments the cellular immune response against tumors, regardless of the absence of CD137 on tumor cells. These pharmacological agents, when administered systemically, surpass the immune effects of the membrane-bound natural ligand (CD137 or 4-1BB ligand), the activity of which is confined to cell-to-cell interactions. Greater affinity and broader distribution of the CD137 pharmacological agonists cause much more intense receptor crosslinking and stronger intracellular signals than the natural ligand. Target engagement on a variety of immune cell types such as T, natural killer and dendritic cells and on tumor vessels could switch on multiple mechanisms of action. As an agonist, anti-CD137 monoclonal antibody has entered Phase II clinical trials; elucidation of the mechanisms behind the antitumor efficacy requires further research in mice and patients to understand and rationally combine these new treatments.
CD137(也称为4-1BB)是一种表面共刺激糖蛋白,最初被描述为存在于活化的T淋巴细胞上。用单克隆抗体或其他激动剂部分对该分子进行人工刺激,可在治疗上增强针对肿瘤的细胞免疫反应,而不管肿瘤细胞上是否存在CD137。这些药物制剂全身给药时,其免疫效果超过膜结合天然配体(CD137或4-1BB配体)的免疫效果,后者的活性局限于细胞间相互作用。与天然配体相比,CD137药物激动剂具有更高的亲和力和更广泛的分布,可导致更强烈的受体交联和更强的细胞内信号。在多种免疫细胞类型(如T细胞、自然杀伤细胞和树突状细胞)以及肿瘤血管上的靶点结合可开启多种作用机制。作为一种激动剂,抗CD137单克隆抗体已进入II期临床试验;阐明抗肿瘤疗效背后的机制需要在小鼠和患者中进一步研究,以理解并合理联合这些新疗法。