Academic Respiratory Unit, School of Clinical Sciences, University of Bristol, Bristol BS10 5NB, UK.
Department of Pharmacy and Pharmacology, University of Bath, Bath BA1 1RL, UK.
Int J Mol Sci. 2018 Apr 24;19(5):1269. doi: 10.3390/ijms19051269.
Interstitial lung disease (ILD) encompasses a group of heterogeneous diseases characterised by varying degrees of aberrant inflammation and fibrosis of the lung parenchyma. This may occur in isolation, such as in idiopathic pulmonary fibrosis (IPF) or as part of a wider disease process affecting multiple organs, such as in systemic sclerosis. Anti-Vascular Endothelial Growth Factor (anti-VEGF) therapy is one component of an existing broad-spectrum therapeutic option in IPF (nintedanib) and may become part of the emerging therapeutic strategy for other ILDs in the future. This article describes our current understanding of VEGF biology in normal lung homeostasis and how changes in its bioavailability may contribute the pathogenesis of ILD. The complexity of VEGF biology is particularly highlighted with an emphasis on the potential non-vascular, non-angiogenic roles for VEGF in the lung, in both health and disease.
间质性肺疾病(ILD)是一组异质性疾病,其特征是肺实质的炎症和纤维化程度不同。这种疾病可能是孤立的,如特发性肺纤维化(IPF),也可能是影响多个器官的更广泛疾病过程的一部分,如系统性硬化症。抗血管内皮生长因子(anti-VEGF)治疗是 IPF 中现有广谱治疗选择的一个组成部分(尼达尼布),并且可能成为未来其他ILD 治疗策略的一部分。本文描述了我们目前对正常肺稳态中 VEGF 生物学的理解,以及其生物利用度的变化如何导致ILD 的发病机制。VEGF 生物学的复杂性尤其突出,重点是 VEGF 在肺中的非血管、非血管生成作用,无论是在健康还是疾病中。