Aaron Diamond AIDS Research Center, 455 First Avenue, New York, NY 10016, USA.
AIDS and Cancer Virus Program, Leidos Biomedical Research, Frederick National Laboratory, Frederick, MD 21702, USA.
Science. 2014 Jun 20;344(6190):1401-5. doi: 10.1126/science.1250761.
Primate lentiviruses exhibit narrow host tropism, reducing the occurrence of zoonoses but also impairing the development of optimal animal models of AIDS. To delineate the factors limiting cross-species HIV-1 transmission, we passaged a modified HIV-1 in pigtailed macaques that were transiently depleted of CD8(+) cells during acute infection. During adaptation over four passages in macaques, HIV-1 acquired the ability to antagonize the macaque restriction factor tetherin, replicated at progressively higher levels, and ultimately caused marked CD4(+) T cell depletion and AIDS-defining conditions. Transient treatment with an antibody to CD8 during acute HIV-1 infection caused rapid progression to AIDS, whereas untreated animals exhibited an elite controller phenotype. Thus, an adapted HIV-1 can cause AIDS in macaques, and stark differences in outcome can be determined by immunological perturbations during early infection.
灵长类慢病毒表现出狭窄的宿主嗜性,降低了人畜共患病的发生,但也妨碍了艾滋病最佳动物模型的发展。为了阐明限制 HIV-1 跨物种传播的因素,我们在恒河猴中传代了一种经过修饰的 HIV-1,在急性感染期间,恒河猴的 CD8(+)细胞被短暂耗尽。在恒河猴中经过四次传代的适应过程中,HIV-1获得了拮抗恒河猴限制因子 tetherin 的能力,复制水平逐渐升高,最终导致明显的 CD4(+)T 细胞耗竭和艾滋病定义的条件。在急性 HIV-1 感染期间,短暂用抗 CD8 抗体治疗会导致快速进展为艾滋病,而未治疗的动物则表现出精英控制者的表型。因此,适应性 HIV-1 可以在恒河猴中引起艾滋病,而早期感染期间的免疫干扰可以决定明显不同的结果。