Schnell Frederick J, Alberts-Grill Noah, Evavold Brian D
Department of Microbiology and Immunology, Emory University, Atlanta, GA 30322, USA.
J Immunol. 2009 Feb 15;182(4):1829-35. doi: 10.4049/jimmunol.0801798.
One mechanism viruses use to subvert immune surveillance is through mutation of MHC contact residues of antigenic epitopes that weaken T cell recognition to the point that the immune system is ignorant of the infection. However, in contrast to ignorance, results presented herein demonstrate that intracellular signaling does occur upon stimulation with a lymphocytic choriomeningitis virus-derived escape mutant as demonstrated by the sustained activation of Src homology 2 domain-containing protein tyrosine phosphatase (SHP-1). In addition to the increased SHP-1 activity, we found that the mutated epitope failed to induce oxidation of SHP-1, further enhancing enzymatic activity. Sustained activation of SHP-1 in a reduced form correlated with ERK and early growth response gene 1 activation and failure of T cells to commit to the effector lineage. Thus, instead of immune ignorance, these studies demonstrate the activation of a negative signaling pathway that actively suppresses T cell responses and limits recognition of viral escape mutants.
病毒用于颠覆免疫监视的一种机制是通过抗原表位的MHC接触残基发生突变,这种突变会削弱T细胞识别能力,直至免疫系统对感染毫无察觉。然而,与免疫忽视不同的是,本文呈现的结果表明,在用淋巴细胞性脉络丛脑膜炎病毒衍生的逃逸突变体刺激后,细胞内信号传导确实会发生,这一点通过含Src同源2结构域的蛋白酪氨酸磷酸酶(SHP-1)的持续激活得以证明。除了SHP-1活性增加外,我们还发现突变的表位未能诱导SHP-1氧化,从而进一步增强了酶活性。SHP-1以还原形式持续激活与ERK和早期生长反应基因1的激活以及T细胞无法分化为效应细胞谱系有关。因此,这些研究表明,并非免疫忽视,而是激活了一条负信号通路,该通路会积极抑制T细胞反应并限制对病毒逃逸突变体的识别。