Department of Medical Sciences, Pulmonology, Faculty of Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, 400012 Cluj-Napoca, Romania.
I Department of Pulmonology, "Leon Daniello" Clinical Hospital of Pulmonology, 400371 Cluj-Napoca, Romania.
Biomolecules. 2024 Feb 20;14(3):247. doi: 10.3390/biom14030247.
Interstitial Lung Disease (ILD) involves lung disorders marked by chronic inflammation and fibrosis. ILDs include pathologies like idiopathic pulmonary fibrosis (IPF), connective tissue disease-associated ILD (CTD-ILD), hypersensitivity pneumonitis (HP) or sarcoidosis. Existing data covers pathogenesis, diagnosis (especially using high-resolution computed tomography), and treatments like antifibrotic agents. Despite progress, ILD diagnosis and management remains challenging with significant morbidity and mortality. Recent focus is on Progressive Fibrosing ILD (PF-ILD), characterized by worsening symptoms and fibrosis on HRCT. Prevalence is around 30%, excluding IPF, with a poor prognosis. Early diagnosis is crucial for optimizing outcomes in PF-ILD individuals. The lung microbiome comprises all the microorganisms that are in the respiratory tract. Relatively recent research try to evaluate its role in respiratory disease. Healthy lungs have a diverse microbial community. An imbalance in bacterial composition, changes in bacterial metabolic activities, or changes in bacterial distribution within the lung termed dysbiosis is linked to conditions like COPD, asthma and ILDs. We conducted a systematic review of three important scientific data base using a focused search strategy to see how the lung microbiome is involved in the progression of ILDs. Results showed that some differences in the composition and quality of the lung microbiome exist in ILDs that show progressive fibrosing phenotype. The results seem to suggest that the lung microbiota could be involved in ILD progression, but more studies showing its exact pathophysiological mechanisms are needed.
间质性肺疾病(ILD)是一种以慢性炎症和纤维化为特征的肺部疾病。ILD 包括特发性肺纤维化(IPF)、结缔组织疾病相关的 ILD(CTD-ILD)、过敏性肺炎(HP)或结节病等病理类型。现有数据涵盖了发病机制、诊断(特别是使用高分辨率计算机断层扫描)以及抗纤维化药物等治疗方法。尽管取得了进展,但 ILD 的诊断和管理仍然具有挑战性,其发病率和死亡率都很高。最近的研究重点是进行性纤维化 ILD(PF-ILD),其特征是 HRCT 上症状恶化和纤维化。不包括 IPF 在内,PF-ILD 的患病率约为 30%,预后较差。早期诊断对于优化 PF-ILD 患者的预后至关重要。肺部微生物组是指存在于呼吸道中的所有微生物。相对较新的研究试图评估其在呼吸道疾病中的作用。健康的肺部有一个多样化的微生物群落。细菌组成的失衡、细菌代谢活性的变化或细菌在肺部的分布变化,称为菌群失调,与 COPD、哮喘和 ILD 等疾病有关。我们使用聚焦搜索策略对三个重要的科学数据库进行了系统评价,以了解肺部微生物组如何参与 ILD 的进展。结果表明,在表现出进行性纤维化表型的 ILD 中,肺部微生物组的组成和质量存在一些差异。结果似乎表明,肺部微生物群可能参与 ILD 进展,但需要更多研究来显示其确切的病理生理机制。