Martinez Fernando D
Swift-McNear Professor of Pediatrics, Director, Arizona Respiratory Center, The University of Arizona, 1501 N. Campbell Avenue, Suite 2349 Tucson, AZ 85724-5030, USA.
Proc Am Thorac Soc. 2005;2(2):157-61. doi: 10.1513/pats.200504-044AW.
Viral lower respiratory tract illnesses occurring during the first years of life are associated with increased risk of subsequent asthma, but the mechanisms involved have not been completely elucidated. The available evidence suggests that the factors that explain this connection are heterogeneous. Children who start life with lower levels of airway function appear to be more prone to transient forms of wheezing in the first years of life. "Intrinsic" bronchial hyperresponsiveness, that is, that measured shortly after birth and unrelated to markers of atopy, has been reported to predict both early life wheezing and wheezing occurring during the early school years, independent of atopy. It has also been suggested that both decreased interferon-gamma responses measured before any viral lower respiratory illness and increased interferon-gamma responses measured at the time of the illness may predispose to such illnesses. Children in whom the former mechanism is involved should be expected to be more atopic later in life, whereas those with the latter mechanism should be less likely to be atopic. This may explain why early viral respiratory illnesses have been found to be both protective against and a risk factor for subsequent atopy in different studies. Current evidence thus suggests that different and often apparently contradictory mechanisms related to airway function, structure, and immune responsiveness may explain the association between viral lower airway illness in early life and subsequent asthma. Future preventive and therapeutic strategies will need to address the specific mechanisms that explain this association in different groups of subjects.
生命最初几年发生的病毒性下呼吸道疾病与随后患哮喘的风险增加有关,但其中涉及的机制尚未完全阐明。现有证据表明,解释这种关联的因素是异质性的。出生时气道功能水平较低的儿童在生命的最初几年似乎更容易出现短暂性喘息。据报道,“内在性”支气管高反应性,即在出生后不久测量且与特应性标志物无关的支气管高反应性,可独立于特应性预测早期喘息和学龄早期出现的喘息。也有人提出,在任何病毒性下呼吸道疾病之前测量的干扰素-γ反应降低以及在疾病发生时测量的干扰素-γ反应增加都可能易患此类疾病。预计涉及前一种机制的儿童在生命后期更易患特应性疾病,而涉及后一种机制的儿童患特应性疾病的可能性较小。这可能解释了为什么在不同的研究中,早期病毒性呼吸道疾病既被发现对随后的特应性疾病有保护作用,又是一个危险因素。因此,目前的证据表明,与气道功能、结构和免疫反应性相关的不同且往往明显相互矛盾的机制可能解释了生命早期病毒性下气道疾病与随后哮喘之间的关联。未来的预防和治疗策略将需要针对不同组受试者中解释这种关联的具体机制。