Department of Medicine, University of Chicago, Chicago, IL, USA; Committee on Immunology, University of Chicago, Chicago, IL, USA.
Committee on Microbiology, University of Chicago, Chicago, IL, USA.
Cell Host Microbe. 2018 Nov 14;24(5):677-688.e5. doi: 10.1016/j.chom.2018.10.004. Epub 2018 Nov 1.
Intestinal reovirus infection can trigger T helper 1 (T1) immunity to dietary antigen, raising the question of whether other viruses can have a similar impact. Here we show that the acute CW3 strain of murine norovirus, but not the persistent CR6 strain, induces T1 immunity to dietary antigen. This property of CW3 is dependent on its major capsid protein, a virulence determinant. Transcriptional profiling of mesenteric lymph nodes following infection reveals an immunopathological signature that does not segregate with protective immunity but with loss of oral tolerance, in which interferon regulatory factor 1 is critical. These data show that viral capacity to trigger specific inflammatory pathways at sites where T cell responses to dietary antigens take place interferes with the development of tolerance to an oral antigen. Collectively, these data provide a foundation for the development of therapeutic strategies to prevent T1-mediated complex immune disorders triggered by viral infections.
肠道呼肠孤病毒感染可引发针对膳食抗原的辅助性 T 细胞 1(T1)免疫,由此引发人们思考其他病毒是否可能具有类似的影响。在这里,我们发现急性 CW3 型鼠诺如病毒株而非持续性 CR6 型鼠诺如病毒株可诱导针对膳食抗原的 T1 免疫。CW3 型病毒株的这一特性取决于其主要衣壳蛋白,该蛋白是一种毒力决定因素。感染后肠系膜淋巴结的转录组分析揭示了一种免疫病理特征,该特征与保护性免疫无关,而是与口服耐受丧失相关,其中干扰素调节因子 1 是关键。这些数据表明,病毒在发生针对膳食抗原的 T 细胞反应的部位引发特定炎症途径的能力干扰了对口服抗原的耐受形成。总之,这些数据为开发治疗策略以预防病毒感染引发的 T1 介导的复杂免疫紊乱提供了基础。