首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Cutting Edge: Novel vaccination modality provides significant protection against mucosal infection by highly pathogenic simian immunodeficiency virus
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Cutting Edge: Novel vaccination modality provides significant protection against mucosal infection by highly pathogenic simian immunodeficiency virus

机译:前沿:新型的疫苗接种方式可有效抵抗高致病性猿猴免疫缺陷病毒的粘膜感染

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Vaccine-induced protection against infection by HIV or highly pathogenic and virulent SIV strains has been limited. In a proof-of-concept study, we show that a novel vaccine approach significantly protects rhesus macaques from mucosal infection by the highly pathogenic strain SIVmac251. We vaccinated three cohorts of 12 macaques each with live, irradiated vaccine cells secreting the modified endoplasmic reticulum chaperone gp96-Ig. Cohort 1 was vaccinated with cells secreting gp96SIVIg carrying SIV peptides. In addition, Cohort 2 received recombinant envelope protein SIV-gp120. Cohort 3 was injected with cells secreting gp96-Ig (no SIV Ags) vaccines. Cohort 2 was protected from infection. After seven rectal challenges with highly pathogenic SIVmac251, the hazard ratio was 0.27, corresponding to a highly significant, 73% reduced risk for viral acquisition. The apparent success of the novel vaccine modality recommends further study. ? 2013 by The American Association of Immunologists, Inc.
机译:疫苗诱导的针对HIV或高致病性和强毒SIV株感染的保护作用有限。在概念验证研究中,我们显示了一种新颖的疫苗方法可有效保护猕猴免受高致病性菌株SIVmac251的粘膜感染。我们给三个队列的每只12只猕猴接种了活的,经过辐射的疫苗细胞,这些细胞分泌了修饰的内质网伴侣蛋白gp96-Ig。队列1用分泌携带SIV肽的gp96SIVIg的细胞接种。另外,队列2接受了重组包膜蛋白SIV-gp120。向队列3注射分泌gp96-Ig(无SIV Ags)疫苗的细胞。队列2被保护免受感染。在使用高致病性的SIVmac251进行七次直肠挑战后,危险比为0.27,对应于病毒获取的风险显着降低73%。新疫苗形式的明显成功建议进一步研究。 ?美国免疫学家协会,2013年。

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