首页> 外文期刊>The Journal of Infectious Diseases >Antiviral activity of single-dose PRO 140, a CCR5 monoclonal antibody, in HIV-infected adults.
【24h】

Antiviral activity of single-dose PRO 140, a CCR5 monoclonal antibody, in HIV-infected adults.

机译:单剂量PRO 140(一种CCR5单克隆抗体)在HIV感染的成年人中的抗病毒活性。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: The current goal of human immunodeficiency virus type 1 (HIV-1) therapy is to maximally suppress viral replication. Securing this goal requires new drugs and treatment classes. The chemokine receptor CCR5 provides an entry portal for HIV-1, and PRO 140 is a humanized monoclonal antibody that binds to CCR5 and potently inhibits CCR5-tropic (R5) HIV-1 in vitro. METHODS: A randomized, double-blind, placebo-controlled, dose-escalating study was conducted in 39 individuals with HIV-1 RNA levels or =5000 copies/mL, CD4(+) cell counts > or =250 cells/microL, no antiretroviral therapy for 3 months, and only R5 HIV-1 detectable. Cohorts were randomized 3:10 to receive placebo or doses of PRO 140 of 0.5, 2, or 5 mg/kg. Subjects were monitored for 58 days for safety, antiviral effects, and serum concentrations of PRO 140. RESULTS: PRO 140 was generally well tolerated and demonstrated potent, rapid, prolonged, and dose-dependent antiviral activity. Mean reductions in HIV-1 RNA level of 0.58 log(10), 1.20 log(10) (P= .0002) and 1.83 log(10) (P= .0001) were observed for the 0.5-, 2-, and 5-mg/kg dose groups, respectively. Reductions in mean viral load of > or =10-fold were observed within 4 days and persisted for 2-3 weeks after treatment. CONCLUSIONS: This trial established clear proof of concept for PRO 140 as a potent antiretroviral agent with extended activity after a single dose. TRIAL REGISTRATION: ISRCTN Register: ISRCTN45537485 .
机译:背景:人类免疫缺陷病毒1型(HIV-1)治疗的当前目标是最大程度地抑制病毒复制。确保这一目标需要新的药物和治疗方法。趋化因子受体CCR5提供了HIV-1的进入门户,PRO 140是一种人源化单克隆抗体,可与CCR5结合并在体外有效抑制CCR5-tropic(R5)HIV-1。方法:对39名HIV-1 RNA水平或= 5000拷贝/ mL,CD4(+)细胞计数>或= 250细胞/ microL的个体进行了一项随机,双盲,安慰剂对照的剂量递增研究。抗逆转录病毒疗法治疗3个月,仅可检测到R5 HIV-1。将队列3:10随机接受安慰剂或0.5、2或5 mg / kg的PRO 140剂量。监测受试者58天的安全性,抗病毒作用和PRO 140的血清浓度。结果:PRO 140一般耐受性良好,并表现出有效,快速,长期和剂量依赖性的抗病毒活性。对于0.5-,2-和5观察到HIV-1 RNA水平平均降低了0.58 log(10),1.20 log(10)(P = .0002)和1.83 log(10)(P = .0001) -mg / kg剂量组。在4天内观察到平均病毒载量减少了>或= 10倍,并在治疗后持续了2-3周。结论:该试验为PRO 140作为有效的抗逆转录病毒药,单剂给药后具有延长的活性建立了明确的概念证明。试用注册:ISRCTN注册:ISRCTN45537485。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 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