...
首页> 外文期刊>Antiviral therapy >Safety, pharmacokinetics and immune effects in normal volunteers of CPG 10101 (ACTILOM), an investigational synthetic toll-like receptor 9 agonist.
【24h】

Safety, pharmacokinetics and immune effects in normal volunteers of CPG 10101 (ACTILOM), an investigational synthetic toll-like receptor 9 agonist.

机译:CPG 10101(ACTILOM)的正常志愿者的安全性,药代动力学和免疫作用,CPG 10101是一种研究性合成的收费样受体9激动剂。

获取原文
获取原文并翻译 | 示例
           

摘要

CPG 10101 (ACTILON) is a novel potent and selective unmethylated cytidine-phosphate-guanosine (CpG)-containing oligodeoxynucleotide agonist of Toll-like receptor 9 (TLR9) being developed for the treatment of chronic infections such as HCV. OBJECTIVES AND METHODS: In this randomized, double-blind, placebo-controlled Phase I study in 48 normal volunteers, we investigated the safety, pharmacokinetic parameters and immune effects of subcutaneous administration of CPG 10101. Five sequential escalating doses from 0.25 to 20 mg were administered twice, 14 days apart. In addition, a 4 mg dose was administered twice weekly for four weeks. RESULTS: A maximum tolerated dose was not reached and the adverse event profile was consistent with the known immunostimulatory effects of TLR9 agonists, mostly consisting of injection site reactions or flu-like symptoms that were generally mild in intensity. CPG 10101 induced interferons, cytokines and chemokines in a pattern consistent with the biology of TLR9. The most sensitive marker was IP-10/CXCL10, whose induction was detected in some subjects even at the 0.25 mg dose. Some cytokines showed transient circulating levels, while the levels of others such as the antiviral cytokine 2',5'-oligoadenylate synthetase were sustained for several days. CONCLUSION: This study warrants further investigation of CPG 10101 for the treatment of chronic infections such as HCV.
机译:CPG 10101(ACTILON)是一种新型强效且选择性的含Toll样受体9(TLR9)的未甲基化胞苷-磷酸-鸟苷(CpG)寡聚脱氧核苷酸激动剂,正在开发中,可用于治疗HCV等慢性感染。目的和方法:在这项针对48位正常志愿者的随机,双盲,安慰剂对照的I期研究中,我们研究了CPG 10101皮下给药的安全性,药代动力学参数和免疫效果。从0.25到20 mg的5种连续递增剂量两次给药,间隔14天。另外,每周两次给予4 mg剂量,持续4周。结果:未达到最大耐受剂量,不良事件特征与TLR9激动剂的已知免疫刺激作用一致,主要由注射部位反应或强度一般较轻的流感样症状组成。 CPG 10101以与TLR9生物学一致的模式诱导干扰素,细胞因子和趋化因子。最敏感的标记是IP-10 / CXCL10,即使在0.25 mg剂量下,在某些受试者中也能检测到其诱导作用。一些细胞因子显示出短暂的循环水平,而其他细胞因子(例如抗病毒细胞因子2',5'-寡腺苷酸合成酶)的水平持续数天。结论:该研究值得进一步研究CPG 10101用于治疗慢性感染如HCV。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号