Reddehase Matthias J
Institute for Virology, Johannes Gutenberg University, Hochhaus am Augustusplatz, 55101 Mainz, Germany.
Nat Rev Immunol. 2002 Nov;2(11):831-44. doi: 10.1038/nri932.
CD8+ T cells are the main effector cells for the immune control of cytomegaloviruses. To subvert this control, human and mouse cytomegaloviruses each encode a set of immune-evasion proteins, referred to here as immunoevasins, which interfere specifically with the MHC class I pathway of antigen processing and presentation. Although the concerted action of immunoevasins prevents the presentation of certain viral peptides, other viral peptides escape this blockade conditionally or constitutively and thereby provide the molecular basis of immune surveillance by CD8+ T cells. The definition of viral antigenic peptides that are presented despite the presence of immunoevasins adds a further dimension to the prediction of protective epitopes for use in vaccines.
CD8+ T细胞是巨细胞病毒免疫控制的主要效应细胞。为了颠覆这种控制,人类和小鼠巨细胞病毒各自编码一组免疫逃避蛋白,在此称为免疫逃逸蛋白,它们特异性干扰抗原加工和呈递的MHC I类途径。尽管免疫逃逸蛋白的协同作用阻止了某些病毒肽的呈递,但其他病毒肽有条件地或组成性地逃避了这种阻断,从而为CD8+ T细胞的免疫监视提供了分子基础。尽管存在免疫逃逸蛋白,但仍能呈递的病毒抗原肽的定义为预测疫苗中使用的保护性表位增添了新的维度。