Department of Microbiology and Immunology, School of Medicine University of North Carolina at Chapel Hill, North Carolina 27599-7435, USA.
J Virol. 2010 Sep;84(17):8530-8. doi: 10.1128/JVI.00727-10. Epub 2010 Jun 23.
Immune responses and the components of protective immunity following norovirus infection in humans are poorly understood. Although antibody responses following norovirus infection have been partially characterized, T cell responses in humans remain largely undefined. In contrast, T cells have been shown to be essential for viral clearance of mouse norovirus (MNV) infection. In this paper, we demonstrate that CD4(+) T cells secrete gamma interferon (IFN-gamma) in response to stimulation with MNV virus-like particles (VLPs) after MNV infection, supporting earlier reports for norovirus-infected mice and humans. Utilizing this model, we immunized mice with alphavirus vectors (Venezuelan equine encephalitis [VEE] virus replicon particles [VRPs]) expressing Norwalk virus (NV) or Farmington Hills virus (FH) virus-like particles to evaluate T cell epitopes shared between human norovirus strains. Stimulation of splenocytes from norovirus VRP-immunized mice with overlapping peptides from complete libraries of the NV or FH capsid proteins revealed specific amino acid sequences containing T cell epitopes that were conserved within genoclusters and genogroups. Immunization with heterologous norovirus VRPs resulted in specific cross-reactive IFN-gamma secretion profiles following stimulation with NV and FH peptides in the mouse. Identification of unique strain-specific and cross-reactive epitopes may provide insight into homologous and heterologous T cell-mediated norovirus immunity and provide a platform for the study of norovirus-induced cellular immunity in humans.
人类感染诺如病毒后免疫反应和保护性免疫的成分了解甚少。虽然已经部分描述了诺如病毒感染后的抗体反应,但人类的 T 细胞反应在很大程度上仍未得到定义。相比之下,T 细胞已被证明对于清除小鼠诺如病毒(MNV)感染是必不可少的。在本文中,我们证明 CD4(+)T 细胞在 MNV 感染后对 MNV 病毒样颗粒(VLPs)的刺激会分泌γ干扰素(IFN-gamma),这支持了先前对感染诺如病毒的小鼠和人类的报告。利用该模型,我们用表达诺如病毒(NV)或法明顿希尔斯病毒(FH)病毒样颗粒的甲病毒载体(委内瑞拉马脑炎[VEE]病毒复制子颗粒[VRP])对小鼠进行免疫接种,以评估人类诺如病毒株之间共享的 T 细胞表位。用 NV 或 FH 衣壳蛋白完整文库的重叠肽刺激来自诺如病毒 VRP 免疫小鼠的脾细胞,揭示了含有 T 细胞表位的特定氨基酸序列,这些表位在基因簇和基因组内保守。用异源诺如病毒 VRPs 免疫导致在小鼠中用 NV 和 FH 肽刺激后出现特异性交叉反应性 IFN-gamma 分泌谱。鉴定独特的株特异性和交叉反应性表位可能有助于了解同源和异源 T 细胞介导的诺如病毒免疫,并为研究人类诺如病毒诱导的细胞免疫提供平台。