Han Junyan, Takeda Katsuyuki, Gelfand Erwin W
Division of Cell Biology, Department of Pediatrics, National Jewish Health, Denver, CO 80206, USA.
Pulm Med. 2011;2011:748038. doi: 10.1155/2011/748038. Epub 2011 Jul 2.
Respiratory syncytial virus (RSV) is a common cause of severe lower respiratory tract diseases (bronchiolitis and pneumonia) during infancy and early childhood. There is increasing evidence which indicates that severe pulmonary disease caused by RSV infection in infancy is associated with recurrent wheezing and development of asthma later in childhood. However, the underlying mechanisms linking RSV infection to persistent airway hyperresponsiveness and dysfunction are not fully defined. To study these processes in ways which are not available in humans, animal models have been established and have provided valuable insight into the pathophysiology of RSV-induced disease. In this paper, we discuss experimental models of RSV infection in mice and highlight a new investigative approach in which mice are initially infected as neonates and then reinfected later in life. The findings shed light on the mechanisms underlying the association between early severe RSV infection and development of asthma later in childhood.
呼吸道合胞病毒(RSV)是婴幼儿期严重下呼吸道疾病(细支气管炎和肺炎)的常见病因。越来越多的证据表明,婴儿期RSV感染所致的严重肺部疾病与儿童后期反复喘息及哮喘的发生有关。然而,将RSV感染与持续性气道高反应性和功能障碍联系起来的潜在机制尚未完全明确。为了以人体无法实现的方式研究这些过程,已建立了动物模型,这些模型为RSV诱导疾病的病理生理学提供了有价值的见解。在本文中,我们讨论了小鼠RSV感染的实验模型,并重点介绍了一种新的研究方法,即先在新生小鼠期进行感染,然后在其生命后期再次感染。这些研究结果揭示了早期严重RSV感染与儿童后期哮喘发生之间关联的潜在机制。