Schindler Michael, Würfl Stephanie, Benaroch Philippe, Greenough Thomas C, Daniels Rod, Easterbrook Philippa, Brenner Matthias, Münch Jan, Kirchhoff Frank
Department of Virology, Universitätsklinikum, 89081 Ulm, Germany.
J Virol. 2003 Oct;77(19):10548-56. doi: 10.1128/jvi.77.19.10548-10556.2003.
Recently, it has been demonstrated that the human immunodeficiency virus type 1 (HIV-1) Nef from laboratory strains down-modulates cell surface expression of mature major histocompatibility complex class II (MHC-II) molecules, while up-regulating surface expression of the invariant chain (Ii) associated with immature MHC-II (P. Stumptner-Cuvelette, S. Morchoisne, M. Dugast, S. Le Gall, G. Raposo, O. Schwartz, and P. Benaroch, Proc. Natl. Acad. Sci. USA 98:12144-12149, 2001). These Nef functions could contribute to impaired CD4(+)-T-helper-cell responses found in HIV-1-infected patients with progressive disease. However, it is currently unknown whether nef alleles derived from HIV-1-infected individuals or from other primate lentiviruses also modulate MHC-II and Ii. In the present study, we demonstrate that both activities are conserved among primary HIV-1 nef alleles, as well as among HIV-2 and simian immunodeficiency virus (SIV) nef alleles. Down-modulation of mature MHC-II required high levels of Nef expression. In contrast, surface expression of Ii was already strongly increased at low to medium levels of Nef expression. Notably, nef genes derived from two of four HIV-1-infected long-term nonprogressors did not up-regulate Ii, whereas nef alleles derived from 10 individuals with progressive disease were active in this assay. Unlike other in vitro Nef functions, the average activity of Nef in modulating MHC-II and Ii surface expression did not change significantly during the course of infection. Mutational analysis confirmed that MHC-II down- and Ii up-regulation are functionally separable from each other and from other Nef functions and identified acidic residues, located at the base of the flexible C-proximal loop of Nef, that are critical for increased Ii expression. Overall, our results suggest that the ability of Nef to interfere with MHC-II antigen presentation might play a role in AIDS pathogenesis.
最近有研究表明,实验室毒株的人类免疫缺陷病毒1型(HIV-1)Nef可下调成熟主要组织相容性复合体II类(MHC-II)分子的细胞表面表达,同时上调与未成熟MHC-II相关的恒定链(Ii)的表面表达(P. Stumptner-Cuvelette、S. Morchoisne、M. Dugast、S. Le Gall、G. Raposo、O. Schwartz和P. Benaroch,《美国国家科学院院刊》98:12144 - 12149,2001年)。这些Nef功能可能导致在患有进展性疾病的HIV-1感染患者中发现的CD4(+)辅助性T细胞反应受损。然而,目前尚不清楚源自HIV-1感染个体或其他灵长类慢病毒的nef等位基因是否也调节MHC-II和Ii。在本研究中,我们证明这两种活性在原发性HIV-1 nef等位基因以及HIV-2和猴免疫缺陷病毒(SIV)nef等位基因中都是保守的。成熟MHC-II的下调需要高水平的Nef表达。相比之下,在低至中等水平的Nef表达时,Ii的表面表达就已经显著增加。值得注意的是,来自四名HIV-1感染的长期不进展者中的两名的nef基因并未上调Ii,而来自10名进展性疾病患者的nef等位基因在该实验中具有活性。与其他体外Nef功能不同,Nef在调节MHC-II和Ii表面表达方面的平均活性在感染过程中没有显著变化。突变分析证实,MHC-II下调和Ii上调在功能上彼此可分离,并且与其他Nef功能可分离,并确定了位于Nef柔性C近端环底部的酸性残基,这些残基对于增加Ii表达至关重要。总体而言,我们的结果表明Nef干扰MHC-II抗原呈递的能力可能在艾滋病发病机制中起作用。