Holtappels Rafaela, Thomas Doris, Reddehase Matthias J
Institute for Virology, Johannes Gutenberg University, Hochhaus am Augustusplatz, 55101 Mainz, Germany1.
J Gen Virol. 2000 Dec;81(Pt 12):3037-3042. doi: 10.1099/0022-1317-81-12-3037.
The two sister cytomegaloviruses (CMVs), human and murine CMV, have both evolved immune evasion functions that interfere with the major histocompatibility complex class I (MHC-I) pathway of antigen processing and presentation and are effectual in the early (E) phase of virus gene expression. However, studies on murine CMV have shown that E-phase immune evasion is leaky. An E-phase protein involved in immune evasion, namely m04-gp34, was found to simultaneously account for an antigenic peptide presented by the MHC-I molecule D(d). Recent work has demonstrated the induction of protective immunity specific for the E-phase protein M84-p65, one of two murine CMV homologues of the human CMV matrix protein UL83-pp65. In this study, the identification of the MHC-I K(d)-restricted M84 peptide (297)AYAGLFTPL(305) is documented. This peptide is the third antigenic peptide described for murine CMV and the second that escapes immunosubversive mechanisms.
人类巨细胞病毒(CMV)和鼠巨细胞病毒这两种姐妹病毒都进化出了免疫逃避功能,它们会干扰主要组织相容性复合体I类(MHC-I)的抗原加工和呈递途径,并且在病毒基因表达的早期(E)阶段发挥作用。然而,对鼠巨细胞病毒的研究表明,E期免疫逃避存在漏洞。一种参与免疫逃避的E期蛋白,即m04-gp34,被发现同时负责由MHC-I分子D(d)呈递的一种抗原肽。最近的研究表明,针对E期蛋白M84-p65可诱导产生保护性免疫,M84-p65是人类CMV基质蛋白UL83-pp65的两种鼠巨细胞病毒同源物之一。在本研究中,记录了MHC-I K(d)限制性M84肽(297)AYAGLFTPL(305)的鉴定。该肽是描述的第三种鼠巨细胞病毒抗原肽,也是第二种逃避免疫颠覆机制的肽。