首页> 外文期刊>European journal of clinical microbiology and infectious diseases: Official publication of the European Society of Clinical Microbiology >Phase I clinical trial with HIV-1 gp160 plasmid vaccine in HIV-1-infected asymptomatic subjects.
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Phase I clinical trial with HIV-1 gp160 plasmid vaccine in HIV-1-infected asymptomatic subjects.

机译:HIV-1 gp160质粒疫苗在HIV-1感染的无症状受试者中进行的I期临床试验。

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The aim of the study was to investigate the safety of an HIV-1 gp160 plasmid vaccine. Four asymptomatic HIV-1-infected subjects with CD4+ lymphocyte counts >500/microl were injected with four times 400 microg of HIV-1 modified gp160 env and rev coding DNA vaccine at 0, 4, 10 and 28 weeks. Safety parameters, including autoimmune antibodies as well as CD4+/CD8+ cell counts and HIV-1 plasma concentrations, were monitored for 52 weeks after the first vaccine application. Follow-up data for more than 3 years are now available. The DNA vaccine proved to be safe and, specifically, did not induce anti-DNA autoimmune antibodies. Vaccination had no long-term effects on the CD4+/CD8+ lymphocyte counts, plasma HIV-1 RNA concentrations or disease progression. The present data supplement published data from Philadelphia, USA, where a dose-escalating study (30-300 microg) with the same HIV-1 DNA vaccine was performed.
机译:该研究的目的是研究HIV-1 gp160质粒疫苗的安全性。在0、4、10和28周时,对4例无症状的HIV-1感染的CD4 +淋巴细胞计数> 500 /μl的受试者注射400克HIV-1修饰的gp160 env和rev编码DNA疫苗的四倍。首次接种疫苗后52周,应监测安全性参数,包括自身免疫抗体以及CD4 + / CD8 +细胞计数和HIV-1血浆浓度。现在可以提供3年以上的跟踪数据。 DNA疫苗被证明是安全的,特别是不会诱导抗DNA自身免疫抗体。疫苗接种对CD4 + / CD8 +淋巴细胞计数,血浆HIV-1 RNA浓度或疾病进展没有长期影响。本数据补充资料来自美国费城,在该数据中使用相同的HIV-1 DNA疫苗进行了剂量递增研究(30-300微克)。

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