Department of Infectious Diseases, Second Affiliated Hospital of Medical College of Xi'an Jiaotong University, Xi'an, China.
Department of Infectious Diseases, Xi'an Children's Hospital, Xi'an, China.
J Med Virol. 2018 Apr;90(4):692-698. doi: 10.1002/jmv.25000. Epub 2018 Jan 5.
Hand, foot, and mouth disease (HFMD) caused by enterovirus 71 (EV71) presents with a wide variety of clinical manifestations. Host immune response is a factor that influences disease susceptibility and severity. We investigated the potential association of gene polymorphisms in the pattern recognition receptor (PRR) pathway with the risk and severity of EV71 infection. A total of 180 EV71 HFMD cases (108 severe case; 72 mild cases) were enrolled. A group of 201 sex- and age-matched children was included as a control. All subjects were genotyped for the most common single-nucleotide polymorphisms (SNPs) in the PRR and the PRR signaling pathway using the SNPscan multiple SNP typing method. Binary logistic regression analysis revealed statistically significant differences in polymorphism of RIG-1 between patients and controls (rs3739674 G vs C: OR = 1.502, 95%CI: 1.120-2.014; rs9695310 G vs C: OR = 1.782, 95%CI: 1.312-2.419). Polymorphisms of RIG-1 rs3739674 (G vs C: OR = 2.047, 95%CI: 1.307-3.205) and TLR3 rs5743305 (A vs T: OR = 0.346, 95%CI: 0.212-0.566) were found to be associated with disease severity. The results indicated that RIG-1 (rs3739674 and rs9695310) polymorphisms are associated with an increased risk of EV71-induced HFMD in Chinese children, whereas RIG-1 rs3739674 and TLR3 rs5743305 polymorphisms are associated with disease severity. These findings support an important role of innate immune mechanism in EV71 infection.
手足口病(HFMD)由肠道病毒 71 型(EV71)引起,临床表现多样。宿主免疫反应是影响疾病易感性和严重程度的一个因素。我们研究了模式识别受体(PRR)途径中基因多态性与 EV71 感染风险和严重程度的潜在关联。共纳入 180 例 EV71 手足口病病例(108 例重症病例;72 例轻症病例)。选择 201 名性别和年龄匹配的儿童作为对照组。采用 SNPscan 多重 SNP 分型法对 PRR 和 PRR 信号通路中最常见的单核苷酸多态性(SNP)进行基因分型。二元逻辑回归分析显示,患者与对照组之间 RIG-1 多态性存在统计学差异(rs3739674 G 与 C:OR=1.502,95%CI:1.120-2.014;rs9695310 G 与 C:OR=1.782,95%CI:1.312-2.419)。RIG-1 rs3739674(G 与 C:OR=2.047,95%CI:1.307-3.205)和 TLR3 rs5743305(A 与 T:OR=0.346,95%CI:0.212-0.566)多态性与疾病严重程度相关。结果表明,RIG-1(rs3739674 和 rs9695310)多态性与中国儿童 EV71 诱导的 HFMD 风险增加相关,而 RIG-1 rs3739674 和 TLR3 rs5743305 多态性与疾病严重程度相关。这些发现支持先天免疫机制在 EV71 感染中的重要作用。