Laboratory of Pathogenesis of Viral Infections, Department of Public Health and Pediatric Sciences, University of Turin, Turin, Italy.
Neonatal Unit, Department of Public Health and Pediatric Sciences, University of Turin, Turin, Italy.
Front Immunol. 2021 Apr 9;12:532484. doi: 10.3389/fimmu.2021.532484. eCollection 2021.
Human cytomegalovirus (HCMV) infection often leads to systemic disease in immunodeficient patients and congenitally infected children. Despite its clinical significance, the exact mechanisms contributing to HCMV pathogenesis and clinical outcomes have yet to be determined. One of such mechanisms involves HCMV-mediated NK cell immune response, which favors viral immune evasion by hindering NK cell-mediated cytolysis. This process appears to be dependent on the extent of HCMV genetic variation as high levels of variability in viral genes involved in immune escape have an impact on viral pathogenesis. However, the link between viral genome variations and their functional effects has so far remained elusive. Thus, here we sought to determine whether inter-host genetic variability of HCMV influences its ability to modulate NK cell responses to infection. For this purpose, five HCMV clinical isolates from a previously characterized cohort of pediatric patients with confirmed HCMV congenital infection were evaluated by next-generation sequencing (NGS) for genetic polymorphisms, phylogenetic relationships, and multiple-strain infection. We report variable levels of genetic characteristics among the selected clinical strains, with moderate variations in genome regions associated with modulation of NK cell functions. Remarkably, we show that different HCMV clinical strains differentially modulate the expression of several ligands for the NK cell-activating receptors NKG2D, DNAM-1/CD226, and NKp30. Specifically, the DNAM-1/CD226 ligand PVR/CD155 appears to be predominantly upregulated by fast-replicating ("aggressive") HCMV isolates. On the other hand, the NGK2D ligands ULBP2/5/6 are downregulated regardless of the strain used, while other NK cell ligands (i.e., MICA, MICB, ULBP3, Nectin-2/CD112, and B7-H6) are not significantly modulated. Furthermore, we show that IFN-γ; production by NK cells co-cultured with HCMV-infected fibroblasts is directly proportional to the aggressiveness of the HCMV clinical isolates employed. Interestingly, loss of NK cell-modulating genes directed against NK cell ligands appears to be a common feature among the "aggressive" HCMV strains, which also share several gene variants across their genomes. Overall, even though further studies based on a higher number of patients would offer a more definitive scenario, our findings provide novel mechanistic insights into the impact of HCMV genetic variability on NK cell-mediated immune responses.
人巨细胞病毒(HCMV)感染常导致免疫缺陷患者和先天性感染儿童发生全身疾病。尽管其具有临床意义,但导致 HCMV 发病机制和临床结果的确切机制尚未确定。其中一种机制涉及 HCMV 介导的 NK 细胞免疫反应,该反应通过阻碍 NK 细胞介导的细胞溶解来促进病毒的免疫逃逸。这一过程似乎依赖于 HCMV 遗传变异的程度,因为参与免疫逃逸的病毒基因的高度变异性对病毒发病机制有影响。然而,病毒基因组变异与其功能效应之间的联系迄今仍未得到阐明。因此,我们在这里试图确定 HCMV 宿主间遗传变异是否影响其调节 NK 细胞对感染反应的能力。为此,我们通过下一代测序(NGS)对来自先前表征的儿科患者先天性 HCMV 感染队列的五株 HCMV 临床分离株进行了遗传多态性、系统发育关系和多株感染评估。我们报告了所选临床株之间遗传特征的不同水平,与调节 NK 细胞功能相关的基因组区域存在中度变异。值得注意的是,我们表明,不同的 HCMV 临床株以不同的方式调节 NK 细胞激活受体 NKG2D、DNAM-1/CD226 和 NKp30 的几种配体的表达。具体而言,DNAM-1/CD226 配体 PVR/CD155 似乎主要由快速复制(“侵袭性”)HCMV 分离株上调。另一方面,无论使用何种菌株,NKG2D 配体 ULBP2/5/6 均下调,而其他 NK 细胞配体(即 MICA、MICB、ULBP3、Nectin-2/CD112 和 B7-H6)则无明显变化。此外,我们表明,与感染了 HCMV 的成纤维细胞共培养的 NK 细胞产生 IFN-γ与所用 HCMV 临床分离株的侵袭性直接成正比。有趣的是,针对 NK 细胞配体的 NK 细胞调节基因的缺失似乎是“侵袭性”HCMV 株的共同特征,这些株在其基因组中也具有多个基因变体。总体而言,尽管基于更多患者的进一步研究将提供更明确的情况,但我们的研究结果为 HCMV 遗传变异性对 NK 细胞介导的免疫反应的影响提供了新的机制见解。