Batten C Jane, De Rose Robert, Wilson Kim M, Agy Michael B, Chea Socheata, Stratov Ivan, Montefiori David C, Kent Stephen J
Department of Microbiology and Immunology, University of Melbourne, Victoria 3010, Australia.
AIDS Res Hum Retroviruses. 2006 Jun;22(6):580-8. doi: 10.1089/aid.2006.22.580.
The global impact of HIV/AIDS intensifies the need for a preventive vaccine and nonhuman primate models can help provide critical insights into effective immunity. Pigtail macaques (Macaca nemestrina) are increasingly studied as a nonhuman primate model for AIDS. We compared the virologic and immunologic characteristics of HIV-1, SIV, and SHIV infection of naive pigtail macaques across a series of preclinical HIV vaccine studies. SIVmac251 and SIVmac239 infection of naive pigtail macaques resulted in a gradual decline in peripheral CD4+ T cells in the setting of high levels of viremia, approximating most closely human infection of HIV-1. In contrast, the CXCR4-utilizing SHIVmn229 virus resulted in rapid depletion of CD4+ T cells and minimal generation of humoral or cellular immune responses, similar to that observed with SHIV89.6P infection of rhesus macaques. Infection with the CCR5-utilizing, rhesus macaque passaged, SHIVSF162P3 resulted in some overall CD4+ T cell decline, however, three of eight macaques naturally control SHIVSF162P3 viremia to very low levels in the setting of robust adaptive immunity. Despite attempts at infecting pigtail macaques with HIV-1 strains passaged in juvenile pigtail macaques in vivo or in PBMC isolated from pigtail macaques in vitro, only lower nonsustained levels of viral replication were observed. Our results provide a series of virologic models with which to evaluate potential AIDS vaccines in pigtail macaques.
艾滋病毒/艾滋病的全球影响凸显了对预防性疫苗的需求,而非人灵长类动物模型有助于深入了解有效的免疫反应。猪尾猕猴(食蟹猴)作为艾滋病的非人灵长类动物模型正受到越来越多的研究。在一系列临床前艾滋病毒疫苗研究中,我们比较了初免猪尾猕猴感染HIV-1、SIV和SHIV后的病毒学和免疫学特征。初免猪尾猕猴感染SIVmac251和SIVmac239后,在病毒血症水平较高的情况下,外周血CD4+T细胞逐渐减少,与人类感染HIV-1的情况最为接近。相比之下,利用CXCR4的SHIVmn229病毒导致CD4+T细胞迅速耗竭,体液或细胞免疫反应产生极少,这与恒河猴感染SHIV89.6P时观察到的情况相似。感染利用CCR5的、经恒河猴传代的SHIVSF162P3后,总体上CD4+T细胞有所下降,然而,八只猕猴中有三只在强大的适应性免疫情况下,能将SHIVSF162P3病毒血症自然控制在非常低的水平。尽管尝试用在幼年猪尾猕猴体内传代的HIV-1毒株或从猪尾猕猴分离的外周血单核细胞(PBMC)在体外感染猪尾猕猴,但仅观察到较低的、无法持续的病毒复制水平。我们的结果提供了一系列病毒学模型,可用于评估猪尾猕猴的潜在艾滋病疫苗。