Stevenson P G, Efstathiou S, Doherty P C, Lehner P J
Division of Virology, Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, United Kingdom.
Proc Natl Acad Sci U S A. 2000 Jul 18;97(15):8455-60. doi: 10.1073/pnas.150240097.
The gamma-herpesviruses, in contrast to the alpha- and beta-herpesviruses, are not known to inhibit antigen presentation to CD8(+) cytotoxic T lymphocytes (CTLs) during lytic cycle replication. However, murine gamma-herpesvirus 68 causes a chronic lytic infection in CD4(+) T cell-deficient mice despite the persistence of a substantial CTL response, suggesting that CTL evasion occurs. Here we show that, distinct from host protein synthesis shutoff, gamma-herpesvirus 68 down-regulates surface MHC class I expression on lytically infected fibroblasts and inhibits their recognition by antigen-specific CTLs. The viral K3 gene, encoding a zinc-finger-containing protein, dramatically reduced the half-life of nascent class I molecules and the level of surface MHC class I expression and was by itself sufficient to block antigen presentation. The homologous K3 and K5 genes of the related Kaposi's sarcoma-associated virus also inhibited antigen presentation and decreased cell surface expression of HLA class I antigens. Thus it appears that an immune evasion strategy shared by at least two gamma-herpesviruses allows continued lytic infection in the face of strong CTL immunity.
与α-疱疹病毒和β-疱疹病毒不同,γ-疱疹病毒在裂解周期复制过程中并不抑制向CD8(+)细胞毒性T淋巴细胞(CTL)的抗原呈递。然而,尽管存在大量CTL反应,小鼠γ-疱疹病毒68仍在CD4(+) T细胞缺陷小鼠中引起慢性裂解感染,这表明发生了CTL逃避。在这里我们表明,与宿主蛋白合成关闭不同,γ-疱疹病毒68下调裂解感染的成纤维细胞表面MHC I类分子的表达,并抑制抗原特异性CTL对它们的识别。编码含锌指蛋白的病毒K3基因显著缩短了新生I类分子的半衰期以及表面MHC I类分子的表达水平,其本身就足以阻断抗原呈递。相关的卡波西肉瘤相关病毒的同源K3和K5基因也抑制抗原呈递并降低HLA I类抗原的细胞表面表达。因此,至少两种γ-疱疹病毒共有的免疫逃避策略似乎使得在面对强大的CTL免疫时仍能持续进行裂解感染。