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中性粒细胞皮肤病及其在哮喘和其他呼吸道合并症发病机制中的意义:一篇叙述性综述。

Neutrophilic Dermatoses and Their Implication in Pathophysiology of Asthma and Other Respiratory Comorbidities: A Narrative Review.

机构信息

Department of Dermatology, Case Western Reserve University, Cleveland, USA.

Department of Health Sciences (DISSAL), School of Public Health, University of Genoa, Genoa, Italy.

出版信息

Biomed Res Int. 2019 Jun 10;2019:7315274. doi: 10.1155/2019/7315274. eCollection 2019.

Abstract

Neutrophilic dermatoses (ND) are a polymorphous group of noncontagious dermatological disorders that share the common histological feature of a sterile cutaneous infiltration of mature neutrophils. Clinical manifestations can vary from nodules, pustules, and bulla to erosions and ulcerations. The etiopathogenesis of neutrophilic dermatoses has continuously evolved. Accumulating genetic, clinical, and histological evidence point to NDs being classified in the spectrum of autoinflammatory conditions. However, unlike the monogenic autoinflammatory syndromes where a clear multiple change in the inflammasome structure/function is demonstrated, NDs display several proinflammatory abnormalities, mainly driven by IL-1, IL-17, and tumor necrosis factor-alpha (TNF-a). Additionally, because of the frequent association with extracutaneous manifestations where neutrophils seem to play a crucial role, it was plausible also to consider NDs as a cutaneous presentation of a systemic neutrophilic condition. Neutrophilic dermatoses are more frequently recognized in association with respiratory disorders than by chance alone. The combination of the two, particularly in the context of their overlapping immune responses mediated primarily by neutrophils, raises the likelihood of a common neutrophilic systemic disease or an aberrant innate immunity disorder. Associated respiratory conditions can serve as a trigger or may develop or be exacerbated secondary to the uncontrolled skin disorder. Physicians should be aware of the possible pulmonary comorbidities and apply this knowledge in the three steps of patients' management, work-up, diagnosis, and treatment. In this review, we attempt to unravel the pathophysiological mechanisms of this association and also present some evidence for the role of targeted therapy in the treatment of both conditions.

摘要

中性粒细胞皮肤病(ND)是一组非传染性皮肤病,具有共同的组织学特征,即成熟中性粒细胞的无菌性皮肤浸润。临床表现可从结节、脓疱和大疱到糜烂和溃疡不等。中性粒细胞皮肤病的病因发病机制不断演变。越来越多的遗传、临床和组织学证据表明,中性粒细胞皮肤病被归类为自身炎症性疾病谱。然而,与多基因突变的自身炎症性综合征不同,后者表现出炎症小体结构/功能的明显改变,中性粒细胞皮肤病表现出几种促炎异常,主要由白细胞介素 1(IL-1)、白细胞介素 17(IL-17)和肿瘤坏死因子-α(TNF-α)驱动。此外,由于与中性粒细胞似乎发挥关键作用的皮肤外表现频繁相关,也可以将中性粒细胞皮肤病视为全身性中性粒细胞疾病的皮肤表现。中性粒细胞皮肤病与呼吸系统疾病的关联比偶然关联更为常见。两者的结合,特别是在主要由中性粒细胞介导的重叠免疫反应的背景下,增加了共同的系统性中性粒细胞疾病或异常先天免疫紊乱的可能性。相关的呼吸系统疾病可能作为触发因素,也可能继发于不受控制的皮肤疾病而发生或加重。医生应注意可能的肺部合并症,并将这一知识应用于患者管理、检查、诊断和治疗的三个步骤中。在这篇综述中,我们试图揭示这种关联的病理生理学机制,并提供一些证据表明靶向治疗在这两种疾病治疗中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8011/6590566/e27795a97a23/BMRI2019-7315274.001.jpg

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