一种脱氧核糖核酸/改良安卡拉猴免疫缺陷病毒疫苗可引发强大但具有年龄依赖性的保护作用。

Strong, but Age-Dependent, Protection Elicited by a Deoxyribonucleic Acid/Modified Vaccinia Ankara Simian Immunodeficiency Virus Vaccine.

机构信息

Yerkes National Primate Research Center, Emory University , Atlanta, Georgia.

Department of Microbiology , Immunology and Parasitology, Louisiana State University Health Sciences Center , New Orleans.

出版信息

Open Forum Infect Dis. 2016 Feb 11;3(1):ofw034. doi: 10.1093/ofid/ofw034. eCollection 2016 Jan.

Abstract

Background.  In this study, we analyzed the protective efficacy of a simian immunodeficiency virus (SIV) macaque 239 (SIVmac239) analogue of the clinically tested GOVX-B11 deoxyribonucleic acid (DNA)/modified vaccinia Ankara (MVA) human immunodeficiency virus vaccine. Methods.  The tested vaccine used a DNA immunogen mutated to mimic the human vaccine and a regimen with DNA deliveries at weeks 0 and 8 and MVA deliveries at weeks 16 and 32. Twelve weekly rectal challenges with 0.3 animal infectious doses of SIV sootey mangabey E660 (SIVsmE660) were administered starting at 6 months after the last immunization. Results.  Over the first 6 rectal exposures to SIVsmE660, <10-year-old tripartite motif-containing protein 5 (TRIM5)α-permissive rhesus macaques showed an 80% reduction in per-exposure risk of infection as opposed to a 46% reduction in animals over 10 years old; and, over the 12 challenges, they showed a 72% as opposed to a 10% reduction. Analyses of elicited immune responses suggested that higher antibody responses in the younger animals had played a role in protection. Conclusions.  The simian analogue of the GOVX-B11 HIV provided strong protection against repeated rectal challenges in young adult macaques.

摘要

背景

在这项研究中,我们分析了一种猴免疫缺陷病毒(SIV)猕猴 239(SIVmac239)类似物的保护效力,该类似物是经过临床测试的 GOVX-B11 脱氧核糖核酸(DNA)/改良安卡拉痘苗(MVA)人类免疫缺陷病毒疫苗的类似物。方法:测试疫苗使用了一种 DNA 免疫原,该免疫原经过突变以模拟人类疫苗,并且采用 DNA 接种方案,在第 0 周和第 8 周进行接种,在第 16 周和第 32 周进行 MVA 接种。在最后一次免疫接种后 6 个月,开始每周进行 12 次直肠挑战,每次挑战用 0.3 个动物感染剂量的 SIV sootey mangabey E660(SIVsmE660)。结果:在首次 6 次直肠暴露于 SIVsmE660 中,<10 岁的三结构域蛋白 5(TRIM5)α允许的恒河猴显示出每暴露感染风险降低 80%,而 10 岁以上的动物降低了 46%;在 12 次挑战中,前者降低了 72%,而后者降低了 10%。对诱导免疫反应的分析表明,年轻动物中较高的抗体反应在保护中发挥了作用。结论:GOVX-B11 HIV 的灵长类动物类似物为年轻成年猕猴提供了对重复直肠挑战的强大保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a64a/4800464/7cc8c6d8e1d4/ofw03401.jpg

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