Söderberg Daniel, Segelmark Mårten
Department of Medical and Health Sciences, Linköping University , Linköping , Sweden.
Department of Medical and Health Sciences, Linköping University, Linköping, Sweden; Department of Nephrology, Linköping University, Linköping, Sweden.
Front Immunol. 2016 Jun 30;7:256. doi: 10.3389/fimmu.2016.00256. eCollection 2016.
A group of pauci-immune vasculitides, characterized by neutrophil-rich necrotizing inflammation of small vessels and the presence of antineutrophil cytoplasmic antibodies (ANCAs), is referred to as ANCA-associated vasculitis (AAV). ANCAs against proteinase 3 (PR3) (PR3-ANCA) or myeloperoxidase (MPO) (MPO-ANCA) are found in over 90% of patients with active disease, and these ANCAs are implicated in the pathogenesis of AAV. Dying neutrophils surrounding the walls of small vessels are a histological hallmark of AAV. Traditionally, it has been assumed that these neutrophils die by necrosis, but neutrophil extracellular traps (NETs) have recently been visualized at the sites of vasculitic lesions. AAV patients also possess elevated levels of NETs in the circulation. ANCAs are capable of inducing NETosis in neutrophils, and their potential to do so has been shown to be affinity dependent and to correlate with disease activity. Neutrophils from AAV patients are also more prone to release NETs spontaneously than neutrophils from healthy blood donors. NETs contain proinflammatory proteins and are thought to contribute to vessel inflammation directly by damaging endothelial cells and by activating the complement system and indirectly by acting as a link between the innate and adaptive immune system through the generation of PR3- and MPO-ANCA. Injection of NET-loaded myeloid dendritic cells into mice results in circulating PR3- and MPO-ANCA and the development of AAV-like disease. NETs have also been shown to be essential in a rodent model of drug-induced vasculitis. NETs induced by propylthiouracil could not be degraded by DNaseI, implying that disordered NETs might be important for the generation of ANCAs. NET degradation was also highlighted in another study showing that AAV patients have reduced DNaseI activity resulting in less NET degradation. With this in mind, it might be that prolonged exposure to proteins in the NETs due to the overproduction of NETs and/or reduced clearance of NETs is important in AAV. However, not all ANCAs are pathogenic and some might possibly also aid in the clearance of NETs. A dual role for ANCAs in relation to circulating NET levels has been proposed because a negative correlation was observed between PR3-ANCA and NET remnants in patients in remission.
一组寡免疫性血管炎,其特征为小血管富含中性粒细胞的坏死性炎症以及抗中性粒细胞胞浆抗体(ANCA)的存在,被称为ANCA相关血管炎(AAV)。在超过90%的活动性疾病患者中可检测到抗蛋白酶3(PR3)的ANCA(PR3-ANCA)或抗髓过氧化物酶(MPO)的ANCA(MPO-ANCA),并且这些ANCA与AAV的发病机制有关。小血管壁周围濒死的中性粒细胞是AAV的组织学特征。传统上,人们认为这些中性粒细胞通过坏死死亡,但最近在血管炎性病变部位发现了中性粒细胞胞外陷阱(NETs)。AAV患者循环中的NETs水平也升高。ANCA能够诱导中性粒细胞产生NETosis,并且其诱导能力已被证明具有亲和力依赖性且与疾病活动相关。与健康献血者的中性粒细胞相比,AAV患者的中性粒细胞也更容易自发释放NETs。NETs含有促炎蛋白,被认为通过损伤内皮细胞、激活补体系统直接导致血管炎症,并且通过产生PR3-和MPO-ANCA作为先天免疫系统和适应性免疫系统之间的联系间接导致血管炎症。将负载NETs的髓样树突状细胞注射到小鼠体内会导致循环中的PR3-和MPO-ANCA以及类似AAV疾病的发展。在药物诱导的血管炎啮齿动物模型中,NETs也被证明是必不可少的。丙硫氧嘧啶诱导的NETs不能被DNaseI降解,这意味着紊乱的NETs可能对ANCA的产生很重要。另一项研究也强调了NET降解,该研究表明AAV患者的DNaseI活性降低,导致NET降解减少。考虑到这一点,可能是由于NETs过度产生和/或NETs清除减少导致NETs中蛋白质的长时间暴露在AAV中很重要。然而,并非所有的ANCA都是致病性的,有些可能也有助于清除NETs。有人提出ANCA在循环NET水平方面具有双重作用,因为在缓解期患者中观察到PR3-ANCA与NET残余物之间呈负相关。