Gold Marielle C, Munks Michael W, Wagner Markus, Koszinowski Ulrich H, Hill Ann B, Fling Steven P
Department of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR 97201, USA.
J Immunol. 2002 Jul 1;169(1):359-65. doi: 10.4049/jimmunol.169.1.359.
Although in vitro studies have shown that herpesviruses, including murine CMV (MCMV), encode genes that interfere with the MHC class I pathway, their effects on the CTL response in vivo is unclear. We identified a D(b)-restricted CTL epitope from MCMV M45 by screening an MCMV genomic library using CTL clones isolated from mice infected with MCMV lacking m152. Because m152 severely inhibits CTL recognition of M45 in vitro, we questioned whether an M45-specific response would be generated in mice infected with wild-type MCMV expressing m152. Mice infected with wild-type MCMV or MCMVDelta(m)152 made similar responses to the M45 Ag. Moreover, we saw no skewing of the proportion of M45-specific CD8 T cells within the total MCMV-specific response after infection with MCMV with m152. Despite the profound effect m152 has on presentation of M45 in vitro, it does not affect the immunodominance of M45 in the CTL response in vivo.
尽管体外研究表明,包括鼠巨细胞病毒(MCMV)在内的疱疹病毒编码的基因可干扰MHC I类途径,但其对体内CTL反应的影响尚不清楚。我们通过使用从感染缺乏m152的MCMV的小鼠中分离出的CTL克隆筛选MCMV基因组文库,从MCMV M45中鉴定出一个D(b)限制性CTL表位。由于m152在体外严重抑制CTL对M45的识别,我们质疑在感染表达m152的野生型MCMV的小鼠中是否会产生M45特异性反应。感染野生型MCMV或MCMVΔ(m)152的小鼠对M45抗原产生了相似的反应。此外,在用含m152的MCMV感染后,我们在总的MCMV特异性反应中未发现M45特异性CD8 T细胞比例的偏差。尽管m152在体外对M45的呈递有深远影响,但它并不影响M45在体内CTL反应中的免疫显性。