Schechter Mauro
Universidade Federal do Rio de Janeiro, Av. Brig. Trompowski, CEP 21941-590, Rio de Janeiro, Brazil.
Vaccine. 2002 May 6;20(15):1909-11. doi: 10.1016/s0264-410x(02)00065-8.
We conducted an HIV seroincidence study among high-risk men who have sex with men in Rio de Janeiro to determine whether this population would be suitable for vaccine and non-vaccine HIV prevention studies. There were 34 HIV seroconversions during the follow-up period, for a seroincidence of 3.1 per 100 person-years. The incidence among the youngest members of our cohort was over 8%, an extraordinarily high transmission rate for a homosexual male population. We have used the sensitive/less sensitive ELISA assay to identify a high-risk heterosexual population for intervention studies in Brazil. The estimated seroincidence was 1.9 and 2.8 per 100 person-years among heterosexual females and males, respectively. We are presently conducting a study to investigate behavior changes among 202 participants of a post-sexual-exposure chemoprophylaxis (PEP) study. During a median follow-up of 24 months, there were 11 HIV seroconversions, 10 of which were among non-PEP users. Additionally, we are conducting a phase 2 HIV vaccine trial of the ALVAC-HIV vector vCP1452 alone and in combination with a subunit vaccine, MN rgp120, in healthy adult volunteers. The primary goal of this trial is to define the immunogenicity and confirm the safety of the most promising vector-based vaccine alone and in combination with a recombinant envelope protein vaccine with an established safety and immunogenicity profile. A phase 3 HIV vaccine trial is planned to begin in the next 18-24 months.
我们在里约热内卢的男男性行为高危人群中开展了一项艾滋病毒血清阳转率研究,以确定该人群是否适合进行疫苗及非疫苗预防艾滋病毒的研究。随访期间有34例艾滋病毒血清阳转,血清阳转率为每100人年3.1例。我们队列中最年轻成员的发病率超过8%,这在同性恋男性人群中是极高的传播率。我们已使用敏感性/较低敏感性酶联免疫吸附测定法来确定巴西用于干预研究的高危异性恋人群。异性恋女性和男性的估计血清阳转率分别为每100人年1.9例和2.8例。我们目前正在开展一项研究,调查性暴露后化学预防(PEP)研究的202名参与者的行为变化。在中位随访24个月期间,有11例艾滋病毒血清阳转,其中10例发生在未使用PEP的人群中。此外,我们正在健康成年志愿者中开展一项2期艾滋病毒疫苗试验,研究单独使用ALVAC-HIV载体vCP1452以及将其与亚单位疫苗MN rgp120联合使用的效果。该试验的主要目标是确定最有前景的基于载体的疫苗单独使用以及与具有既定安全性和免疫原性的重组包膜蛋白疫苗联合使用时的免疫原性并确认其安全性。计划在未来18至24个月内开始一项3期艾滋病毒疫苗试验。