[Association of DNA methylation of IFNG gene with no/low response to hepatitis B vaccine in children]

Zhonghua Yu Fang Yi Xue Za Zhi. 2022 Jul 6;56(7):926-931. doi: 10.3760/cma.j.cn112150-20220125-00087.
[Article in Chinese]

Abstract

Objective: To explore the association of DNA methylation with immune response to hepatitis B (HepB) vaccine in Han nationality children from Guangxi province. Methods: A total of 263 children aged 8-9 months who had completed HepB immunization program were recruited from three hospitals in Guangxi province by using unmatched case-control method. Children with the HepB surface antibody concentration(Anti-HBs)<100 mIU/ml was set as the case group and ≥100 mIU/ml as the control group. Multiplex PCR and heavy sulfite sequencing were used to treat the samples. Illumina platform was used for high-throughput DNA methylation sequencing of IFNG gene target regions and CpG sites. Unconditional logistic regression was used to analyze the association between cytosine-phospho-guanosine DNA methylation at 18 loci of IFNG gene and HepB immune response level. Results: There were 104 children in the case group and 159 in the control group. The median (Q1, Q3) level of anti-HBs in two groups were 62.34 (30.06, 98.88) mIU/ml and 1 089.10 (710.35, 1 233.45) mIU/ml. The methylation levels of IFNG_1 gene 44 and 93 locus in the case group were higher than those in the control group (P<0.05). The unconditional logistic regression model showed that the DNA methylation level of IFNG_1 gene at 44 (OR=1.18, 95%CI: 1.03-1.35) and 93 (OR=1.21, 95%CI: 1.07-1.38) locus was associated with the HepB response level. Conclusion: The changes of DNA methylation at locus 44 and 93 of IFNG_1 gene may be relevant factors affecting the response level of HepB in Han nationality children from Guangxi province.

目的: 分析广西汉族儿童IFNG基因DNA甲基化与乙型肝炎(乙肝)疫苗(HepB)免疫应答水平的关联性。 方法: 采用非匹配病例对照方法,招募广西3家医院就诊的263名已完成HepB免疫程序的8~9月龄汉族儿童作为研究对象,将乙肝表面抗体浓度(抗-HBs)<100 mIU/ml设为病例组,≥100 mIU/ml设为对照组。采用多重PCR技术、重亚硫酸盐测序、使用Illumina平台对IFNG基因目标区域及其CpG位点进行DNA甲基化高通量测序。采用非条件logistic回归模型分析IFNG基因18个位点胞嘧啶-磷酸-鸟苷酸 DNA甲基化情况与HepB免疫应答水平的关联。 结果: 病例组(104名)和对照组(159名)抗-HBs[MQ1Q3)]分别为62.34(30.06,98.88)mIU/ml和1 089.10(710.35,1 233.45)mIU/ml。病例组IFNG_1基因44和93位点甲基化水平差异高于对照组(P<0.05),非条件logistic回归模型显示,IFNG_1基因44位点(OR=1.18,95%CI:1.03~1.35)和93位点(OR=1.21,95%CI:1.07~1.38)DNA甲基化水平与HepB应答水平具有相关性。 结论: IFNG_1基因44和93位点DNA甲基化水平改变可能是影响广西汉族儿童HepB应答水平的相关因素。.

MeSH terms

  • Child
  • China
  • DNA Methylation
  • Hepatitis B Antibodies
  • Hepatitis B Surface Antigens
  • Hepatitis B Vaccines*
  • Hepatitis B* / prevention & control
  • Humans
  • Immunization, Secondary
  • Interferon-gamma

Substances

  • Hepatitis B Antibodies
  • Hepatitis B Surface Antigens
  • Hepatitis B Vaccines
  • IFNG protein, human
  • Interferon-gamma