Abolhasani Fatemeh Sadat, Moein Masood, Rezaie Niloofar, Sheikhimehrabadi Parimah, Shafiei Morvarid, Afkhami Hamed, Modaresi Mohammadreza
Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Department of Bacteriology and Virology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Front Microbiol. 2024 Apr 17;15:1356926. doi: 10.3389/fmicb.2024.1356926. eCollection 2024.
Cystic fibrosis (CF) is a genetic ailment caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This autosomal recessive disorder is characterized by diverse pathobiological abnormalities, such as the disorder of CFTR channels in mucosal surfaces, caused by inadequate clearance of mucus and sputum, in addition to the malfunctioning of mucous organs. However, the primary motive of mortality in CF patients is pulmonary failure, which is attributed to the colonization of opportunistic microorganisms, formation of resistant biofilms, and a subsequent decline in lung characteristics. In December 2019, the World Health Organization (WHO) declared the outbreak of the radical coronavirus disease 2019 (COVID-19) as a worldwide public health crisis, which unexpectedly spread not only within China but also globally. Given that the respiration system is the primary target of the COVID-19 virus, it is crucial to investigate the impact of COVID-19 on the pathogenesis and mortality of CF patients, mainly in the context of acute respiratory distress syndrome (ARDS). Therefore, the goal of this review is to comprehensively review the present literature on the relationship between cystic fibrosis, COVID-19 contamination, and development of ARDS. Several investigations performed during the early stages of the virus outbreak have discovered unexpected findings regarding the occurrence and effectiveness of COVID-19 in individuals with CF. Contrary to initial expectancies, the rate of infection and the effectiveness of the virus in CF patients are lower than those in the overall population. This finding may be attributed to different factors, including the presence of thick mucus, social avoidance, using remedies that include azithromycin, the fairly younger age of CF patients, decreased presence of ACE-2 receptors, and the effect of CFTR channel disorder on the replication cycle and infectivity of the virus. However, it is important to notice that certain situations, which include undergoing a transplant, can also doubtlessly boost the susceptibility of CF patients to COVID-19. Furthermore, with an increase in age in CF patients, it is vital to take into account the prevalence of the SARS-CoV-2 virus in this population. Therefore, ordinary surveillance of CF patients is vital to evaluate and save the population from the capability of transmission of the virus given the various factors that contribute to the spread of the SARS-CoV-2 outbreak in this precise organization.
囊性纤维化(CF)是一种由囊性纤维化跨膜传导调节因子(CFTR)基因突变引起的遗传性疾病。这种常染色体隐性疾病的特征是多种病理生物学异常,例如黏膜表面CFTR通道紊乱,这是由于黏液和痰液清除不足以及黏液器官功能失调所致。然而,CF患者死亡的主要原因是肺衰竭,这归因于机会性微生物的定植、耐药生物膜的形成以及随后肺功能的下降。2019年12月,世界卫生组织(WHO)宣布新型冠状病毒病2019(COVID-19)的爆发为全球公共卫生危机,它不仅在中国境内意外传播,而且在全球范围内传播。鉴于呼吸系统是COVID-19病毒的主要攻击目标,研究COVID-19对CF患者发病机制和死亡率的影响至关重要,尤其是在急性呼吸窘迫综合征(ARDS)的背景下。因此,本综述的目的是全面回顾目前关于囊性纤维化、COVID-19感染与ARDS发生之间关系的文献。在病毒爆发的早期阶段进行的多项调查发现了关于COVID-19在CF患者中的发生情况和影响的意外发现。与最初的预期相反,CF患者的感染率和病毒感染效力低于总体人群。这一发现可能归因于不同因素,包括黏稠黏液的存在、社交回避、使用包括阿奇霉素在内的药物、CF患者相对较年轻的年龄、ACE-2受体的减少以及CFTR通道紊乱对病毒复制周期和感染性的影响。然而,需要注意的是,某些情况,如接受移植,也无疑会增加CF患者对COVID-19的易感性。此外,随着CF患者年龄的增长,考虑SARS-CoV-2病毒在该人群中的流行情况至关重要。因此,鉴于导致SARS-CoV-2在这一特定群体中爆发传播的各种因素,对CF患者进行常规监测对于评估和保护该人群免受病毒传播能力的影响至关重要。