Department of Medicine, Washington University School of Medicine, St Louis, MO, USA.
J Allergy Clin Immunol. 2012 May;129(5):1267-1273.e1. doi: 10.1016/j.jaci.2012.02.033. Epub 2012 Mar 27.
Viral respiratory tract infections are the leading cause of acute illness during infancy and are closely linked to chronic inflammatory airway diseases later in life. However, the determinants of susceptibility to acute respiratory tract infections still need to be defined.
We investigated whether the individual variation in antiviral response at birth determines the risk for acute respiratory tract illness in the first year of life.
We studied 82 children who were enrolled in a birth cohort study of inner-city children with at least 1 parent with allergy or asthma. We cultured cord blood monocytes and assessed IFNG and CCL5 mRNA production at 24 hours after inoculation with respiratory syncytial virus. We also monitored the frequency of acute respiratory tract illness at 3-month intervals and analyzed nasal lavage samples for respiratory tract viruses at the time of illness during the first year.
Respiratory tract infection was reported for 88% of subjects, and respiratory tract viruses were recovered in 74% of symptomatic children. We observed a wide range of antiviral responses in cord blood monocytes across the population. Furthermore, a decrease in production of IFNG (but not CCL5) mRNA in response to respiratory syncytial virus infection of monocytes was associated with a significant increase in the frequency of upper respiratory tract infections (r = -0.42, P < .001) and the prevalence of ear and sinus infections, pneumonias, and respiratory-related hospitalizations.
Individual variations in the innate immune response to respiratory tract viruses are detectable even at birth, and these differences predict the susceptibility to acute respiratory tract illness during the first year of life.
病毒呼吸道感染是婴儿期急性疾病的主要原因,并且与生命后期慢性炎症性气道疾病密切相关。然而,易感性的决定因素仍有待确定。
我们研究了出生时抗病毒反应的个体差异是否决定了生命第一年急性呼吸道疾病的风险。
我们研究了 82 名儿童,他们参加了一项城市内儿童的出生队列研究,这些儿童的父母中至少有一位患有过敏或哮喘。我们培养脐带血单核细胞,并在接种呼吸道合胞病毒 24 小时后评估 IFNG 和 CCL5 mRNA 的产生。我们还每隔 3 个月监测急性呼吸道疾病的频率,并在生命第一年患病时分析鼻洗液样本中的呼吸道病毒。
88%的研究对象报告了呼吸道感染,74%的有症状儿童呼吸道病毒被检出。我们观察到人群中脐带血单核细胞的抗病毒反应范围很广。此外,呼吸道合胞病毒感染单核细胞后 IFNG(而不是 CCL5)mRNA 产生减少与上呼吸道感染(r = -0.42,P <.001)、耳和鼻窦感染、肺炎和与呼吸相关的住院治疗的频率显著增加相关。
即使在出生时,也可以检测到对呼吸道病毒的先天免疫反应的个体差异,这些差异预测了生命第一年急性呼吸道疾病的易感性。