University of Zimbabwe, Clinical Trials Research Centre, Harare, Zimbabwe.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
J Acquir Immune Defic Syndr. 2021 May 1;87(1):680-687. doi: 10.1097/QAI.0000000000002649.
BACKGROUND: HIV Vaccine Trials Network 703/HIV Prevention Trials Network 081 is a phase 2b randomized, double-blind, placebo-controlled trial to assess the safety and efficacy of passively infused monoclonal antibody VRC01 in preventing HIV acquisition in heterosexual women between the ages of 18 and 50 years at risk of HIV. Participants were enrolled at 20 sites in Botswana, Kenya, Malawi, Mozambique, South Africa, Tanzania, and Zimbabwe. It is one of the 2 Antibody Mediated Prevention efficacy trials, with HIV Vaccine Trials Network 704/HIV Prevention Trials Network 085, evaluating VRC01 for HIV prevention. METHODS: Intense community engagement was used to optimize participant recruitment and retention. Participants were randomly assigned to receive intravenous VRC01 10 mg/kg, VRC01 30 mg/kg, or placebo in a 1:1:1 ratio. Infusions were given every 8 weeks with a total of 10 infusions and 104 weeks of follow-up after the first infusion. RESULTS: Between May 2016 and September 2018, 1924 women from sub-Saharan Africa were enrolled. The median age was 26 years (interquartile range: 22-30), and 98.9% were Black. Sexually transmitted infection prevalence at enrollment included chlamydia (16.9%), trichomonas (7.2%), gonorrhea (5.7%), and syphilis (2.2%). External condoms (83.2%) and injectable contraceptives (61.1%) were the methods of contraception most frequently used by participants. In total, through April 3, 2020, 38,490 clinic visits were completed with a retention rate of 96% and 16,807 infusions administered with an adherence rate of 98%. CONCLUSIONS: This proof-of-concept, large-scale monoclonal antibody study demonstrates the feasibility of conducting complex trials involving intravenous infusions in high incidence populations in sub-Saharan Africa.
背景:HIV 疫苗试验网络 703/HIV 预防试验网络 081 是一项 2b 期随机、双盲、安慰剂对照试验,旨在评估被动输注单克隆抗体 VRC01 在预防年龄在 18 至 50 岁之间、有 HIV 感染风险的异性恋女性中的安全性和有效性。参与者在博茨瓦纳、肯尼亚、马拉维、莫桑比克、南非、坦桑尼亚和津巴布韦的 20 个地点入组。这是两项抗体介导预防功效试验之一,另一个试验是 HIV 疫苗试验网络 704/HIV 预防试验网络 085,评估 VRC01 预防 HIV 的效果。
方法:采用强化社区参与的方式,以优化参与者的招募和保留。参与者被随机分配接受静脉注射 VRC01 10mg/kg、VRC01 30mg/kg 或安慰剂,比例为 1:1:1。每 8 周输注一次,共输注 10 次,首次输注后随访 104 周。
结果:2016 年 5 月至 2018 年 9 月,来自撒哈拉以南非洲的 1924 名女性入组。中位年龄为 26 岁(四分位间距:22-30 岁),98.9%为黑人。入组时性传播感染的患病率包括衣原体(16.9%)、滴虫病(7.2%)、淋病(5.7%)和梅毒(2.2%)。外部避孕套(83.2%)和注射避孕药(61.1%)是参与者最常使用的避孕方法。截至 2020 年 4 月 3 日,共完成 38490 次就诊,保留率为 96%,共输注 16807 次,依从率为 98%。
结论:这项概念验证、大规模的单克隆抗体研究表明,在撒哈拉以南非洲高发人群中开展涉及静脉输注的复杂试验是可行的。
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