Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
Department of Pathology & Immunology, Baylor College of Medicine, Houston, TX, United States; Biology of Inflammation Center, Baylor College of Medicine, Houston, TX, United States.
Adv Immunol. 2019;142:85-140. doi: 10.1016/bs.ai.2019.05.002. Epub 2019 Jun 29.
The allergic airway diseases, including chronic rhinosinusitis (CRS), asthma, allergic bronchopulmonary mycosis (ABPM) and many others, comprise a heterogeneous collection of inflammatory disorders affecting the upper and lower airways and lung parenchyma that represent the most common chronic diseases of humanity. In addition to their shared tissue tropism, the allergic airway diseases are characterized by a distinct pattern of inflammation involving the accumulation of eosinophils, type 2 macrophages, innate lymphoid cells type 2 (ILC2), IgE-secreting B cells, and T helper type 2 (Th2) cells in airway tissues, and the prominent production of type 2 cytokines including interleukin (IL-) 33, IL-4, IL-5, IL-13, and many others. These factors and related inflammatory molecules induce characteristic remodeling and other changes of the airways that include goblet cell metaplasia, enhanced mucus secretion, smooth muscle hypertrophy, tissue swelling and polyp formation that account for the major clinical manifestations of nasal obstruction, headache, hyposmia, cough, shortness of breath, chest pain, wheezing, and, in the most severe cases of lower airway disease, death due to respiratory failure or disseminated, systemic disease. The syndromic nature of the allergic airway diseases that now include many physiological variants or endotypes suggests that distinct endogenous or environmental factors underlie their expression. However, findings from different perspectives now collectively link these disorders to a single infectious source, the fungi, and a molecular pathogenesis that involves the local production of airway proteinases by these organisms. In this review, we discuss the evidence linking fungi and their proteinases to the surprisingly wide variety of chronic airway and systemic disorders and the immune pathogenesis of these conditions as they relate to environmental fungi. We further discuss the important implications these new findings have for the diagnosis and future therapy of these common conditions.
变应性气道疾病包括慢性鼻-鼻窦炎(CRS)、哮喘、变应性支气管肺曲霉病(ABPM)和许多其他疾病,它们共同构成了一组异质性的炎症性疾病,影响上、下呼吸道和肺实质,是最常见的人类慢性疾病。除了具有共同的组织嗜性外,变应性气道疾病还具有特征性的炎症模式,包括气道组织中嗜酸性粒细胞、2 型巨噬细胞、2 型固有淋巴细胞(ILC2)、IgE 分泌 B 细胞和辅助性 T 细胞 2(Th2)细胞的积聚,以及包括白细胞介素(IL)-33、IL-4、IL-5、IL-13 等在内的 2 型细胞因子的大量产生。这些因素和相关炎症分子诱导气道的特征性重塑和其他变化,包括杯状细胞化生、增强的黏液分泌、平滑肌肥大、组织肿胀和息肉形成,这是鼻腔阻塞、头痛、嗅觉减退、咳嗽、呼吸急促、胸痛、喘息等主要临床表现的原因,在最严重的下气道疾病中,还会因呼吸衰竭或全身性疾病导致死亡。变应性气道疾病的综合征性质现在包括许多生理变异或内型,这表明其表达受到不同内在或环境因素的影响。然而,来自不同角度的研究结果现在共同将这些疾病与单一的感染源——真菌联系起来,并揭示了一个涉及这些生物体局部产生气道蛋白酶的分子发病机制。在这篇综述中,我们讨论了将真菌及其蛋白酶与令人惊讶的多种慢性气道和系统性疾病联系起来的证据,并讨论了这些疾病与环境真菌相关的免疫发病机制。我们进一步讨论了这些新发现对这些常见疾病的诊断和未来治疗的重要意义。