Lemanske Robert F
University of Wisconsin-Madison Medical School, Madison, WI, USA.
Pediatr Allergy Immunol. 2002;13(s15):38-43. doi: 10.1034/j.1399-3038.13.s.15.8.x.
Although asthma is probably a heterogeneous disease or syndrome, three factors and/or events consistently emerge for their ability to significantly influence asthma inception in the first decade of life: immune response aberrations, which appear to be defined best by the concept of cytokine dysregulation; lower respiratory tract infections, in particular respiratory syncytial virus (RSV); and some form of gene-environment interaction that needs to occur at a critical time-period in the development of the immune system or the lung. It remains to be firmly established, however, how any one or all of these factors, either independently or interactively, influence the development of childhood asthma. For example, cytokine dysregulation (T helper 1/T helper 2 imbalance) appears to track best epidemiologically with allergic diseases. As not everyone who undergoes allergic sensitization develops asthma, some other host-environment interaction must need to occur to target this chronic allergic inflammatory response to the lower airway. Some evidence suggests that this event might be an environmental insult in the form of a virus infection, particularly with RSV, which has a predilection for infecting, destroying, and/or in some way biologically altering lower airway epithelium. However, only a fraction of children develop recurrent wheezing following RSV infections, despite the fact that nearly all children have been infected at least once by 2 years of age. Thus, although RSV infections may have the potential of targeting the inflammatory response to the lower airway, they may only be able to do so during a vulnerable time-period during development of the immune system or lung. This developmental component may further reflect important gene-environment interactions that regulate both short- and long-term airway physiological alterations that manifest themselves clinically as childhood asthma. Efforts to determine and define the importance of these three factors to asthma pathogenesis are the focus and goal of the COAST (Childhood Origins of Asthma) project.
尽管哮喘可能是一种异质性疾病或综合征,但有三个因素和/或事件因其在生命的第一个十年中显著影响哮喘发病的能力而始终凸显出来:免疫反应异常,这似乎最好用细胞因子失调的概念来界定;下呼吸道感染,尤其是呼吸道合胞病毒(RSV);以及某种形式的基因-环境相互作用,这种相互作用需要在免疫系统或肺部发育的关键时期发生。然而,这些因素中的任何一个或全部,无论是独立地还是相互作用地,如何影响儿童哮喘的发展,仍有待确切确定。例如,细胞因子失调(辅助性T细胞1/辅助性T细胞2失衡)在流行病学上似乎与过敏性疾病的关联性最强。由于并非每个经历过敏致敏的人都会患上哮喘,所以必然还会发生其他一些宿主-环境相互作用,以使这种慢性过敏性炎症反应靶向于下呼吸道。一些证据表明,这一事件可能是病毒感染形式的环境损伤,尤其是RSV,它倾向于感染、破坏和/或以某种方式在生物学上改变下呼吸道上皮。然而,尽管几乎所有儿童在2岁时至少感染过一次RSV,但只有一小部分儿童在感染RSV后会出现反复喘息。因此,尽管RSV感染可能有将炎症反应靶向于下呼吸道的潜力,但它们可能只能在免疫系统或肺部发育的脆弱时期做到这一点。这种发育因素可能进一步反映了重要的基因-环境相互作用,这些相互作用调节着短期和长期的气道生理改变,这些改变在临床上表现为儿童哮喘。确定和界定这三个因素对哮喘发病机制的重要性的努力是COAST(儿童哮喘的起源)项目的重点和目标。