Blayac Marion, Coll Patrice, Urbach Valérie, Fanen Pascale, Epaud Ralph, Lanone Sophie
Univ Paris Est Creteil, INSERM, IMRB, Creteil, France.
Université Paris Cité and Univ Paris Est Créteil, CNRS, LISA, Paris, France.
Front Physiol. 2022 Jun 2;13:908230. doi: 10.3389/fphys.2022.908230. eCollection 2022.
Cystic fibrosis (CF) is a lethal and widespread autosomal recessive disorder affecting over 80,000 people worldwide. It is caused by mutations of the gene, which encodes an epithelial anion channel. CF is characterized by a great phenotypic variability which is currently not fully understood. Although CF is genetically determined, the course of the disease might also depend on multiple other factors. Air pollution, whose effects on health and contribution to respiratory diseases are well established, is one environmental factor suspected to modulate the disease severity and influence the lung phenotype of CF patients. This is of particular interest as pulmonary failure is the primary cause of death in CF. The present review discusses current knowledge on the impact of air pollution on CF pathogenesis and aims to explore the underlying cellular and biological mechanisms involved in these effects.
囊性纤维化(CF)是一种致命且广泛存在的常染色体隐性疾病,全球有超过8万人受其影响。它由编码上皮阴离子通道的基因突变引起。CF的特点是具有很大的表型变异性,目前尚未完全了解。虽然CF由基因决定,但疾病进程可能还取决于多种其他因素。空气污染对健康的影响及其对呼吸道疾病的作用已得到充分证实,它是一个被怀疑会调节疾病严重程度并影响CF患者肺部表型的环境因素。这一点特别值得关注,因为肺衰竭是CF患者的主要死因。本综述讨论了关于空气污染对CF发病机制影响的现有知识,并旨在探索这些影响所涉及的潜在细胞和生物学机制。