Immune responses to a recombinant human immunodeficiency virus type 1 (HIV-1) gpl60 vaccine among adults with advanced HIV infection. Massachusetts gp160 Working Group.

Journal of human virology Pub Date : 2000-07-01
A DeMaria, L Kunches, K Mayer, C Cohen, P Epstein, B Werner, J Day, J DeCristofaro, S Landers, Y Tang, W Coady
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Abstract

Objective: To assess immunogenicity of recombinant human immunodeficiency virus type 1 (HIV-1) envelope vaccine (rgp160) in late HIV infection.

Study design/methods: HIV-infected volunteers (n = 142), with CD4+ T lymphocyte counts of <400/mm3, were enrolled in a dose-comparison, open-label trial with stratification by CD4+ cell count, randomization to a primary series at two dose levels, and a sub-group receiving interferon-gamma (IFN-gamma) as an adjuvant. Subjects received booster doses of vaccine over a follow-up period of 18-28 months.

Results: At 6 and 12 months, 36% and 38% of participants, respectively, had new or augmented antibody titers (> or =4-fold increase) against one or more gpl60 epitopes (C1, V3, C41, 448C). Delayed-type hypersensitivity (DTH) to intradermal gpl60, initially not present in any participant, developed after immunization in 41%, with higher prevalence in participants receiving the lower dose of vaccine. Both antibody and skin test responses occurred in 20-25% of vaccine recipients. Virtually all antibody and skin test responses occurred in participants with initial CD4+ cell counts of >100 cells/mm3. IFN-gamma had no significant effect on immune response. Immunization was well tolerated. Trends in CD4+ cell count, clinical events, and laboratory findings correlated with baseline CD4+ T lymphocyte count stratum and not with immunization regimen. Opportunistic conditions occurred at expected rates. Viral load trends (p24 antigen in all participants and viral RNA by reverse transcription-polymerase chain reaction in a subset of 26 participants) did not correlate with immunization regimen.

Conclusion: Immunization of patients with advanced HIV infection with rgpl60 resulted in new and augmented humoral and DTH responses, without unexpected significant adverse events or evident clinical benefits attributable to immunization.

晚期HIV感染成人对重组人免疫缺陷病毒1型(HIV-1) gpl60疫苗的免疫应答马萨诸塞州gp160工作组。
目的:评价重组人免疫缺陷病毒1型(HIV-1)包膜疫苗(rgp160)对HIV晚期感染的免疫原性。研究设计/方法:hiv感染志愿者(n = 142), CD4+ T淋巴细胞计数结果:在6个月和12个月时,分别有36%和38%的参与者具有针对一个或多个gpl60表位(C1, V3, C41, 448C)的新抗体滴度或增强抗体滴度(>或=4倍增加)。对皮内gpl60的延迟型超敏反应(DTH),最初不存在于任何参与者中,在接种疫苗后发展为41%,在接受低剂量疫苗的参与者中患病率更高。20-25%的疫苗接种者出现抗体和皮肤试验反应。几乎所有抗体和皮肤试验反应都发生在初始CD4+细胞计数>100细胞/mm3的参与者中。ifn - γ对免疫反应无显著影响。免疫耐受良好。CD4+细胞计数、临床事件和实验室结果的趋势与基线CD4+ T淋巴细胞计数层相关,而与免疫方案无关。机会条件以预期的速率发生。病毒载量趋势(所有参与者的p24抗原和26名参与者的病毒RNA逆转录聚合酶链反应)与免疫方案无关。结论:晚期HIV感染患者接种rgpl60可产生新的和增强的体液和DTH应答,未出现意外的显著不良事件或明显的临床获益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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