Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina 27599, USA.
J Virol. 2010 Feb;84(4):1800-15. doi: 10.1128/JVI.02179-09. Epub 2009 Dec 9.
Norovirus immunity is poorly understood as the limited data available on protection after infection are often contradictory. In contrast to the more prominent GII noroviruses, GI norovirus infections are less frequent in outbreaks. The GI noroviruses display very complex patterns of heterotypic immune responses following infection, and many individuals are highly susceptible to reinfection. To study the immune responses and mechanisms of GI.1 persistence, we built structural models and recombinant virus-like particles (VLPs) of five GI strains: GI.1-1968, GI.1-2001, GI.2-1999, GI.3-1999, and GI.4-2000. Structural models of four GI genotype capsid P domain dimers suggested that intragenotype structural variation is limited, that the GI binding pocket is mostly preserved between genotypes, and that a conserved, surface-exposed epitope may allow for highly cross-reactive immune responses. GI VLPs bound to histo-blood group antigens (HBGAs) including fucose, Lewis, and A antigens. Volunteers infected with GI.1-1968 (n = 10) had significant increases between prechallenge and convalescent reactive IgG for all five GI VLPs measured by enzyme immunoassay. Potential cross-neutralization of GI VLPs was demonstrated by convalescent-phase serum cross-blockade of GI VLP-HBGA interaction. Although group responses were significant for all GI VLPs, each individual volunteer demonstrated a unique VLP blockade pattern. Further, peripheral blood mononuclear cells (PBMCs) were stimulated with each of the VLPs, and secretion of gamma interferon (IFN-gamma) was measured. As seen with blockade responses, IFN-gamma secretion responses differed by individual. Sixty percent responded to at least one GI VLP, with only two volunteers responding to GI.1 VLP. Importantly, four of five individuals with sufficient PBMCs for cross-reactivity studies responded more robustly to other GI VLPs. These data suggest that preexposure history and deceptive imprinting may complicate PBMC and B-cell immune responses in some GI.1-1968-challenged individuals and highlight a potential complication in the design of efficacious norovirus vaccines.
诺如病毒的免疫机制尚不清楚,因为目前关于感染后保护的数据有限,且往往相互矛盾。与更常见的 GII 型诺如病毒相比,GI 型诺如病毒在爆发中的感染频率较低。GI 型诺如病毒在感染后会产生非常复杂的异型免疫反应,许多人极易再次感染。为了研究 GI.1 持续性的免疫反应和机制,我们构建了五个 GI 株的结构模型和重组病毒样颗粒(VLPs):GI.1-1968、GI.1-2001、GI.2-1999、GI.3-1999 和 GI.4-2000。四个 GI 基因型衣壳 P 结构域二聚体的结构模型表明,同型内结构变异有限,GI 结合口袋在基因型之间大多被保留,并且一个保守的、表面暴露的表位可能允许产生高度交叉反应的免疫反应。GI VLPs 与包括岩藻糖、Lewis 和 A 抗原在内的组织血型抗原(HBGAs)结合。10 名感染 GI.1-1968 的志愿者(n=10)通过酶免疫测定法检测到,在挑战前和恢复期,所有五种 GI VLP 的反应性 IgG 均显著增加。通过恢复期血清交叉阻断 GI VLP-HBGA 相互作用,证明了 GI VLPs 的潜在交叉中和作用。虽然所有 GI VLPs 的组反应均有显著意义,但每个个体志愿者都表现出独特的 VLP 阻断模式。此外,用每种 VLP 刺激外周血单核细胞(PBMCs),并测量γ干扰素(IFN-γ)的分泌。与阻断反应一样,IFN-γ的分泌反应因个体而异。60%的人对至少一种 GI VLP 有反应,只有两名志愿者对 GI.1 VLP 有反应。重要的是,在进行交叉反应研究的 5 个人中,有 4 个人对其他 GI VLPs 的反应更强烈。这些数据表明,在某些接受过 GI.1-1968 挑战的个体中,预先暴露史和欺骗性印记可能会使 PBMC 和 B 细胞免疫反应复杂化,并突出了在设计有效诺如病毒疫苗方面的一个潜在并发症。