Mayo Clinic Vaccine Research Group, Mayo Clinic, Rochester, MN 55905, USA.
Vaccine. 2011 Nov 8;29(48):8988-97. doi: 10.1016/j.vaccine.2011.09.043. Epub 2011 Sep 20.
Host antiviral genes are important regulators of antiviral immunity and plausible genetic determinants of immune response heterogeneity after vaccination. We genotyped and analyzed 307 common candidate tagSNPs from 12 antiviral genes in a cohort of 745 schoolchildren immunized with two doses of measles-mumps-rubella (MMR) vaccine. Associations between SNPs/haplotypes and measles virus-specific immune outcomes were assessed using linear regression methodologies in Caucasians and African-Americans. Genetic variants within the DDX58/RIG-I gene, including a coding polymorphism (rs3205166/Val800Val), were associated as single-SNPs (p≤0.017; although these SNPs did not remain significant after correction for false discovery rate/FDR) and in haplotype-level analysis, with measles-specific antibody variations in Caucasians (haplotype allele p-value=0.021; haplotype global p-value=0.076). Four DDX58 polymorphisms, in high LD, demonstrated also associations (after correction for FDR) with variations in both measles-specific IFN-γ and IL-2 secretion in Caucasians (p≤0.001, q=0.193). Two intronic OAS1 polymorphisms, including the functional OAS1 SNP rs10774671 (p=0.003), demonstrated evidence of association with a significant allele-dose-related increase in neutralizing antibody levels in African-Americans. Genotype and haplotype-level associations demonstrated the role of ADAR genetic variants, including a non-synonymous SNP (rs2229857/Arg384Lys; p=0.01), in regulating measles virus-specific IFN-γ Elispot responses in Caucasians (haplotype global p-value=0.017). After correction for FDR, 15 single-SNP associations (11 SNPs in Caucasians and 4 SNPs in African-Americans) still remained significant at the q-value<0.20. In conclusion, our findings strongly point to genetic variants/genes, involved in antiviral sensing and antiviral control, as critical determinants, differentially modulating the adaptive immune responses to live attenuated measles vaccine in Caucasians and African-Americans.
宿主抗病毒基因是抗病毒免疫的重要调节剂,也是疫苗接种后免疫反应异质性的合理遗传决定因素。我们对 745 名接种两剂麻疹-腮腺炎-风疹(MMR)疫苗的学童的 12 个抗病毒基因中的 307 个常见候选标签 SNP 进行了基因分型和分析。在白种人和非裔美国人中,使用线性回归方法评估 SNP/单倍型与麻疹病毒特异性免疫结果之间的关联。DDX58/RIG-I 基因内的遗传变异,包括一个编码多态性(rs3205166/Val800Val),作为单 SNP(p≤0.017;尽管这些 SNP 在经过假发现率/FDR 校正后不再显著)和单倍型水平分析,与白种人麻疹特异性抗体的变化相关(单倍型等位基因 p 值=0.021;单倍型全局 p 值=0.076)。四个 DDX58 多态性,在高度 LD 下,也与白种人麻疹特异性 IFN-γ和 IL-2 分泌的变化相关(经 FDR 校正后 p≤0.001,q=0.193)。两个内含子 OAS1 多态性,包括功能性 OAS1 SNP rs10774671(p=0.003),证明与非裔美国人中和抗体水平的显著等位基因剂量相关增加有关。基因型和单倍型水平的关联表明,ADAR 遗传变异,包括一个非同义 SNP(rs2229857/Arg384Lys;p=0.01),在调节白种人麻疹病毒特异性 IFN-γ Elispot 反应中发挥作用(单倍型全局 p 值=0.017)。经过 FDR 校正后,15 个单 SNP 关联(11 个在白种人和 4 个在非裔美国人中)在 q 值<0.20 时仍具有统计学意义。总之,我们的研究结果强烈表明,参与抗病毒感应和抗病毒控制的遗传变异/基因是关键决定因素,可在白种人和非裔美国人中,差异调节对活减毒麻疹疫苗的适应性免疫反应。