Stott E J, Chan W L, Mills K H, Page M, Taffs F, Cranage M, Greenaway P, Kitchin P
AIDS Collaborating Centre, National Institute for Biological Standards and Control, Hertfordshire, UK.
Lancet. 1990;336(8730):1538-41. doi: 10.1016/0140-6736(90)93310-l.
Cynomolgus macaques were vaccinated with inactivated simian immunodeficiency virus-infected cells and 'Quil-A' as adjuvant at 0, 4, 8, and 36 weeks or at 0, 4, 8, and 16 weeks. 2 weeks later these animals, together with a similar unvaccinated group, were challenged with 10 MID50 (50% monkey infectious doses) of a pool of SIVmac251 previously titrated in vivo. Virus was repeatedly isolated from unvaccinated animals on at least five separate occasions and proviral DNA was detected in circulating lymphocytes by polymerase chain reaction amplification. By contrast, virus and proviral DNA were not found in any of the vaccinated animals. However, the same vaccination regimen used after live virus challenge did not eliminate virus from previously infected macaques.
食蟹猴在第0、4、8和36周或第0、4、8和16周时,用灭活的感染猿猴免疫缺陷病毒的细胞以及“Quil - A”作为佐剂进行接种。2周后,这些动物与一组未接种的相似动物一起,接受10个半数猴感染剂量(MID50)的先前在体内滴定过的SIVmac251病毒库的攻击。在至少五个不同的时间点,从未接种的动物中反复分离出病毒,并且通过聚合酶链反应扩增在循环淋巴细胞中检测到前病毒DNA。相比之下,在任何接种过的动物中均未发现病毒和前病毒DNA。然而,在活病毒攻击后使用相同的接种方案,并不能从先前感染的猕猴中清除病毒。