Jacobson Jeffrey M, Saag Michael S, Thompson Melanie A, Fischl Margaret A, Liporace Ralph, Reichman Richard C, Redfield Robert R, Fichtenbaum Carl J, Zingman Barry S, Patel Mahesh C, Murga Jose D, Pemrick Suzanne M, D'Ambrosio Paul, Michael Marti, Kroger Hans, Ly Hieu, Rotshteyn Yakov, Buice Robert, Morris Stephen A, Stavola Joseph J, Maddon Paul J, Kremer Alton B, Olson William C
Drexel University College of Medicine, Philadelphia, PA 19104, USA.
J Infect Dis. 2008 Nov 1;198(9):1345-52. doi: 10.1086/592169.
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.
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.
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.
This trial established clear proof of concept for PRO 140 as a potent antiretroviral agent with extended activity after a single dose.
ISRCTN Register: ISRCTN45537485 .
目前1型人类免疫缺陷病毒(HIV-1)治疗的目标是最大程度地抑制病毒复制。要实现这一目标需要新的药物和治疗类别。趋化因子受体CCR5为HIV-1提供了一个进入门户,而PRO 140是一种人源化单克隆抗体,它与CCR5结合并在体外有效抑制CCR5嗜性(R5)HIV-1。
对39名HIV-1 RNA水平≥5000拷贝/毫升、CD4(+)细胞计数≥250个/微升、3个月内未接受抗逆转录病毒治疗且仅可检测到R5 HIV-1的个体进行了一项随机、双盲、安慰剂对照、剂量递增研究。各队列按3:10随机分组,接受安慰剂或0.5、2或5毫克/千克剂量的PRO 140。对受试者进行58天的安全性、抗病毒效果及PRO 140血清浓度监测。
PRO 140总体耐受性良好,并表现出强效、快速、持久及剂量依赖性的抗病毒活性。0.5、2和5毫克/千克剂量组的HIV-1RNA水平平均下降分别为0.58 log(10)、1.20 log(10)(P = .0002)和1.83 log(10)(P = .0001)。治疗后4天内平均病毒载量下降≥10倍,并在治疗后持续2至3周。
该试验明确证实了PRO 140作为一种单剂量后具有延长活性的强效抗逆转录病毒药物的概念。
国际标准随机对照试验编号注册库:ISRCTN45537485 。