Proesmans M, De Boeck K
Kinderpneumologie UZ Gasthuisberg, Leuven.
Acta Otorhinolaryngol Belg. 2000;54(3):367-72.
Cystic fibrosis (CF) is an hereditary disease with pancreatic insufficiency and chronic respiratory tract infections leading to irreversible lung damage as its main features. The typical pathogen for the respiratory disease is Pseudomonas aeruginosa. Although the insight into the pathophysiology and genetics of CF have evolved over the past 10 years, there is not yet a full understanding of the increased susceptibility for respiratory infections, specifically with Pseudomonas aeruginosa. In this overview we elucidate the current knowledge and describe the existing hypothesis on the possible links between the pathophysiological defects and the failure of the local defense mechanism in CF airways.
囊性纤维化(CF)是一种遗传性疾病,主要特征为胰腺功能不全和慢性呼吸道感染,可导致不可逆的肺损伤。呼吸道疾病的典型病原体是铜绿假单胞菌。尽管在过去10年里,人们对CF的病理生理学和遗传学的认识有所发展,但对于呼吸道感染,尤其是铜绿假单胞菌感染易感性增加的问题仍未完全了解。在本综述中,我们阐明了当前的知识,并描述了关于CF气道病理生理缺陷与局部防御机制失效之间可能联系的现有假说。