The Generation R Study Group, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Division of Respiratory Medicine and Allergology, Department of Pediatrics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Clin Exp Allergy. 2020 Apr;50(4):499-507. doi: 10.1111/cea.13579. Epub 2020 Feb 27.
Epstein-Barr virus (EBV) and cytomegalovirus (CMV) infection are common in early childhood. CMV infection favours a T-helper-1 and EBV infection a T-helper-2 cell response, possibly leading to disbalanced T-helper cell response, and subsequent risk of asthma or atopy.
To study the associations of EBV and CMV with lung function, asthma and inhalant allergic sensitization at school age.
This study among 3546 children was embedded in a population-based prospective cohort. At age 6 years, serum IgG levels against EBV and CMV were measured by ELISA. At age 10 years, lung function was measured by spirometry, asthma by questionnaire and inhalant allergic sensitization by skin prick test.
Unadjusted models showed that seropositivity for EBV was associated with a higher FEV and FEF (Z-score difference (95% CI): 0.09 (0.02, 0.16) and 0.09 (0.02, 0.15)), while seropositivity for CMV was not. Specific combinations of viruses showed that seropositivity for EBV was only associated with FEV and FEF in the presence of seropositivity for CMV (0.12 (0.04, 0.20)) and 0.08 (0.01, 0.15)). Seropositivity for CMV in the absence of seropositivity for EBV was associated with an increased risk of inhalant allergic sensitization (OR (95% CI): 1.31 (1.02, 1.68)). All effect estimates attenuated into non-significant mainly after adjustment for child's ethnicity. Seropositivity for EBV or CMV was not associated with asthma.
Associations of EBV and CMV infections in early childhood with school-age lung function and inhalant allergic sensitization are explained by ethnicity, or sociodemographic and lifestyle-related factors.
Epstein-Barr 病毒(EBV)和巨细胞病毒(CMV)感染在儿童早期很常见。CMV 感染有利于辅助性 T 细胞 1 反应,而 EBV 感染有利于辅助性 T 细胞 2 反应,这可能导致辅助性 T 细胞反应失衡,并随后增加哮喘或过敏的风险。
研究 EBV 和 CMV 与学龄期儿童肺功能、哮喘和吸入性变应原致敏的相关性。
本研究纳入了一个基于人群的前瞻性队列中的 3546 名儿童。在 6 岁时,通过酶联免疫吸附试验(ELISA)测量血清 IgG 水平对 EBV 和 CMV 的抗体。在 10 岁时,通过肺活量测定法测量肺功能,通过问卷调查测量哮喘,通过皮肤点刺试验测量吸入性变应原致敏情况。
未调整模型显示,EBV 血清阳性与更高的 FEV 和 FEF 相关(Z 分数差异(95%CI):0.09(0.02,0.16)和 0.09(0.02,0.15)),而 CMV 血清阳性则不然。病毒的特定组合显示,只有在 CMV 血清阳性的情况下,EBV 血清阳性才与 FEV 和 FEF 相关(0.12(0.04,0.20)和 0.08(0.01,0.15)))。在没有 EBV 血清阳性的情况下,CMV 血清阳性与吸入性变应原致敏的风险增加相关(OR(95%CI):1.31(1.02,1.68))。所有的效应估计值在主要经过调整儿童种族后都减弱到无统计学意义。EBV 或 CMV 血清阳性与哮喘无关。
儿童早期 EBV 和 CMV 感染与学龄期肺功能和吸入性变应原致敏的相关性可通过种族或社会人口统计学和生活方式相关因素来解释。