Roberts R B, Hollinger F B, Parks W P, Rasheed S, Laurence J, Heseltine P N, Makuch R W, Lubina J A, Johnson K M
New York Hospital-Cornell Medical Center, New York.
AIDS. 1990 Jan;4(1):67-72. doi: 10.1097/00002030-199001000-00009.
A double-blind, randomized, placebo-controlled trial comparing two daily doses of oral ribavirin (600 and 800 mg) and a placebo was performed at four medical centers geographically distributed throughout the USA. One hundred and sixty-four HIV-infected adult men with lymphadenopathy were enrolled over a 2-month period and received active treatment for 24 weeks followed by a 4-week interval during which they did not receive the study drug. A marked interlaboratory variation in HIV isolation from peripheral blood mononuclear cells was observed, underscoring the critical role of quality assurance in similar multicenter trials. Nevertheless, the combined data indicate that ribavirin did not significantly suppress HIV activity (on measurement of reverse transcriptase activity) after week 6 or reduce serum p24 antigenemia.
在美国四个地理位置分散的医疗中心进行了一项双盲、随机、安慰剂对照试验,比较两种每日口服剂量的利巴韦林(600毫克和800毫克)与安慰剂。在2个月的时间里招募了164名患有淋巴结病的HIV感染成年男性,他们接受了24周的积极治疗,随后有4周的间隔期,在此期间他们未接受研究药物。观察到从外周血单核细胞中分离HIV存在显著的实验室间差异,这突出了质量保证在类似多中心试验中的关键作用。然而,综合数据表明,利巴韦林在第6周后并未显著抑制HIV活性(通过逆转录酶活性测量),也未降低血清p24抗原血症。