Bugelski P J, Capocasale R J, Makropoulos D, Marshall D, Fisher P W, Lu J, Achuthanandam R, Spinka-Doms T, Kwok D, Graden D, Volk A, Nesspor T, James I E, Huang C
Centocor Research and Development, Radnor, PA 19087, United States.
J Biotechnol. 2008 Mar 20;134(1-2):171-80. doi: 10.1016/j.jbiotec.2007.12.005. Epub 2007 Dec 27.
CNTO 530 is a 58 kD antibody Fc domain fusion protein, created using Centocor's MIMETIBODY platform, that contains two EMP1 sequences as a pharmacophore. CNTO 530 has no sequence homology with EPO but acts as a novel erythropoietin receptor agonist. In UT-7(EPO) cells, CNTO 530 caused protein phosporylation of the erythropoietin receptor associated signaling pathway (Jak2, STAT5, AKT and ERK1/2). CNTO 530 also rescued these cells from apoptosis and mediated proliferation. In mice, pharmacokinetic analysis showed that CNTO 530 was slowly cleared from circulation with a t(1/2) approximately 40 h. Pharmacodynamic analysis in mice showed that a single sc dose of CNTO 530 caused a long-lived stimulation of erythropoiesis that translated into increases in red blood cell counts and hemoglobin values that were maintained for at least 28 d. In conclusion, CNTO 530 is a long-lived EPO-R agonist that stimulates erythropoiesis in a manner similar to epoetin-alpha. These data suggest that CNTO 530 may be an effective treatment of anemia in humans.
CNTO 530是一种58千道尔顿的抗体Fc结构域融合蛋白,利用Centocor公司的MIMETIBODY平台制备,含有两个作为药效基团的EMP1序列。CNTO 530与促红细胞生成素(EPO)无序列同源性,但作为一种新型促红细胞生成素受体激动剂发挥作用。在UT-7(EPO)细胞中,CNTO 530导致促红细胞生成素受体相关信号通路(Jak2、STAT5、AKT和ERK1/2)的蛋白磷酸化。CNTO 530还使这些细胞免于凋亡并介导增殖。在小鼠中,药代动力学分析表明,CNTO 530从循环中清除缓慢,半衰期约为40小时。小鼠体内的药效学分析表明,单次皮下注射CNTO 530可引起促红细胞生成的长期刺激,转化为红细胞计数和血红蛋白值的增加,并至少维持28天。总之,CNTO 530是一种长效促红细胞生成素受体激动剂,以类似于α-促红细胞生成素的方式刺激促红细胞生成。这些数据表明,CNTO 530可能是治疗人类贫血的有效药物。