Warheit-Niemi Helen I, Hult Elissa M, Moore Bethany B
Department of Microbiology and Immunology University of Michigan Ann Arbor MI USA.
Department of Molecular and Integrative Physiology University of Michigan Ann Arbor MI USA.
Clin Transl Immunology. 2019 Jun 26;8(6):e1065. doi: 10.1002/cti2.1065. eCollection 2019.
Lung fibrosis is characterised by the accumulation of extracellular matrix within the lung and is secondary to both known and unknown aetiologies. This accumulation of scar tissue limits gas exchange causing respiratory insufficiency. The pathogenesis of lung fibrosis is poorly understood, but immunologic-based treatments have been largely ineffective. Despite this, accumulating evidence suggests that innate immune cells and receptors play important modulatory roles in the initiation and propagation of the disease. Paradoxically, while innate immune signalling may be important for the pathogenesis of fibrosis, there is also evidence to suggest that innate immune function against pathogens may be impaired, leading to dysregulated and/or impaired host defence. This review summarises the evidence for this pathologic two-way street, highlights new concepts of pathogenesis and recommends future directions for research emphasis.
肺纤维化的特征是肺内细胞外基质的积累,继发于已知和未知的病因。这种瘢痕组织的积累限制了气体交换,导致呼吸功能不全。肺纤维化的发病机制尚不清楚,但基于免疫的治疗方法大多无效。尽管如此,越来越多的证据表明,天然免疫细胞和受体在该疾病的起始和传播中发挥着重要的调节作用。矛盾的是,虽然天然免疫信号传导可能对纤维化的发病机制很重要,但也有证据表明针对病原体的天然免疫功能可能受损,导致宿主防御失调和/或受损。这篇综述总结了这条病理双向通路的证据,强调了发病机制的新概念,并推荐了未来研究重点的方向。