Department of Pediatrics and Communicable Diseases, University of Michigan Medical School, Medical Sciences Research Building II, 1150 West Medical Center Drive, Ann Arbor, MI, USA.
Department of Pediatrics and Communicable Diseases, University of Michigan Medical School, Medical Sciences Research Building II, 1150 West Medical Center Drive, Ann Arbor, MI, USA; Department of Molecular and Integrative Physiology, University of Michigan Medical School, Medical Sciences Research Building II, 1150 West Medical Center Drive, Ann Arbor, MI, USA.
Immunol Allergy Clin North Am. 2019 Aug;39(3):345-359. doi: 10.1016/j.iac.2019.03.004. Epub 2019 May 7.
Early-life wheezing-associated infections with human rhinovirus (HRV) are strongly associated with the inception of asthma. The immune system of immature mice and humans is skewed toward a type 2 cytokine response. Thus, HRV-infected 6-day-old mice but not adult mice develop augmented type 2 cytokine expression, eosinophilic inflammation, mucous metaplasia, and airway hyperresponsiveness. This asthma phenotype depends on interleukin (IL)-13-producing type 2 innate lymphoid cells, the expansion of which in turn depends on release of the innate cytokines IL-25, IL-33, and thymic stromal lymphopoietin from the airway epithelium. In humans, certain genetic variants may predispose to HRV-induced childhood asthma.
婴幼儿时期与人类鼻病毒(HRV)相关的喘息性感染与哮喘的发生密切相关。未成熟的小鼠和人类的免疫系统偏向于 2 型细胞因子反应。因此,感染 HRV 的 6 天大的小鼠而不是成年小鼠会发展出增强的 2 型细胞因子表达、嗜酸性粒细胞炎症、黏液化生和气道高反应性。这种哮喘表型依赖于白细胞介素(IL)-13 产生的 2 型先天淋巴细胞,其扩增反过来又依赖于气道上皮细胞释放先天细胞因子 IL-25、IL-33 和胸腺基质淋巴生成素。在人类中,某些遗传变异可能易患 HRV 引起的儿童哮喘。