先天免疫系统
生物
免疫学
炎症
血管炎
发病机制
免疫系统
抗中性粒细胞胞浆抗体
蛋白酶3
获得性免疫系统
启动(农业)
疾病
自身免疫
抗体
系统性血管炎
经典补体途径
补体系统
免疫
炎症反应
自身免疫性疾病
作者
Aitana Ignes-Romeu,Laurel E. Hind
标识
DOI:10.1091/mbc.e25-08-0392
摘要
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of rare but severe autoimmune diseases characterized by necrotizing inflammation of small blood vessels, leading to organ damage, particularly in the kidneys and respiratory tract. The current understanding of AAV pathogenesis has moved beyond a simple model of autoantibody-mediated damage to recognize a complex, self-sustaining inflammatory circuit. Central to this circuit is a dysregulated triad between neutrophils, macrophages, and the vascular endothelium. This review synthesizes our current understanding of this innate immune axis, detailing the pathogenic sequence from the initial loss of tolerance to the subsequent inflammatory priming event that triggers the pathogenic activation of neutrophils. The chronicity of AAV arises from powerful feed-forward amplification loops that sustain inflammation, which are cemented by the active suppression of the body's intrinsic resolution pathways. Finally, we discuss how advanced bioengineered platforms, such as vasculitis-on-a-chip models, are essential for deconstructing this complex pathology and are poised to accelerate the development of a new generation of targeted, pro-resolution therapies. This review provides a comprehensive framework for understanding the central role of neutrophil-macrophage cross-talk in the perpetuation of AAV.
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