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Evidence for Recombination of Live, Attenuated Immunodeficiency Virus Vaccine with Challenge Virus to a More Virulent Strain

机译:用减毒病毒将活的减毒的免疫缺陷病毒疫苗重组为更强毒株的证据

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摘要

Live, attenuated immunodeficiency virus vaccines, such as nef deletion mutants, are the most effective vaccines tested in the simian immunodeficiency virus (SIV) macaque model. In two independent studies designed to determine the breadth of protection induced by live, attenuated SIV vaccines, we noticed that three of the vaccinated macaques developed higher set point viral load levels than unvaccinated control monkeys. Two of these vaccinated monkeys developed AIDS, while the control monkeys infected in parallel remained asymptomatic. Concomitant with an increase in viral load, a recombinant of the vaccine virus and the challenge virus could be detected. Therefore, the emergence of more-virulent recombinants of live, attenuated immunodeficiency viruses and less-aggressive wild-type viruses seems to be an additional risk of live, attenuated immunodeficiency virus vaccines.
机译:减毒活免疫减毒活疫苗(例如nef缺失突变体)是在猿猴免疫缺损病毒(SIV)猕猴模型中测试的最有效的疫苗。在两项旨在确定由活的减毒SIV疫苗诱导的保护范围的独立研究中,我们注意到,三只接种过免疫的猕猴比未接种过接种的对照猴具有更高的设定病毒载量水平。这些接种过疫苗的猴子中有两只患有艾滋病,而平行感染的对照猴子则无症状。随着病毒载量的增加,可以检测到疫苗病毒和攻击病毒的重组体。因此,出现弱毒的活的,减毒的免疫缺陷病毒和低攻击性的野生型病毒的重组体似乎是活毒的,减毒的免疫缺陷病毒疫苗的另一风险。

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