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本文引用的文献

1
Clinical consequences of targeting IL-17 and TH17 in autoimmune and allergic disorders.靶向自身免疫和过敏疾病中的 IL-17 和 TH17 的临床后果。
Curr Allergy Asthma Rep. 2013 Dec;13(6):587-95. doi: 10.1007/s11882-013-0361-0.
2
Cytokine targets in airway inflammation.气道炎症中的细胞因子靶点。
Curr Opin Pharmacol. 2013 Jun;13(3):351-61. doi: 10.1016/j.coph.2013.03.013. Epub 2013 May 2.
3
Development and function of group 2 innate lymphoid cells.2 类固有淋巴细胞的发育与功能。
Curr Opin Immunol. 2013 Apr;25(2):148-55. doi: 10.1016/j.coi.2013.02.010. Epub 2013 Apr 4.
4
Lipoxin A4 regulates natural killer cell and type 2 innate lymphoid cell activation in asthma.脂氧素 A4 调节哮喘中自然杀伤细胞和 2 型先天淋巴细胞的激活。
Sci Transl Med. 2013 Feb 27;5(174):174ra26. doi: 10.1126/scitranslmed.3004812.
5
T helper 17 cells in airway diseases: from laboratory bench to bedside.气道疾病中的辅助性 T 细胞 17: 从实验室到临床。
Chest. 2013 Feb 1;143(2):494-501. doi: 10.1378/chest.12-0598.
6
Innate lymphoid cells--how did we miss them?固有淋巴细胞——我们怎么会错过它们呢?
Nat Rev Immunol. 2013 Feb;13(2):75-87. doi: 10.1038/nri3349. Epub 2013 Jan 7.
7
The potential of biologics for the treatment of asthma.生物制剂治疗哮喘的潜力。
Nat Rev Drug Discov. 2012 Dec;11(12):958-72. doi: 10.1038/nrd3792.
8
IL-25 drives remodelling in allergic airways disease induced by house dust mite.IL-25 驱动尘螨诱导的过敏性气道疾病中的重塑过程。
Thorax. 2013 Jan;68(1):82-90. doi: 10.1136/thoraxjnl-2012-202003. Epub 2012 Oct 23.
9
Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA.基于人群的哮喘全基因组关联研究在确认已知和推测的基因座的基础上,进一步鉴定了 HLA 附近的一个新的关联。
PLoS One. 2012;7(9):e44008. doi: 10.1371/journal.pone.0044008. Epub 2012 Sep 28.
10
Epithelial cell-derived IL-25, but not Th17 cell-derived IL-17 or IL-17F, is crucial for murine asthma.上皮细胞衍生的 IL-25,但不是 Th17 细胞衍生的 IL-17 或 IL-17F,对小鼠哮喘至关重要。
J Immunol. 2012 Oct 1;189(7):3641-52. doi: 10.4049/jimmunol.1200461. Epub 2012 Aug 31.

重症哮喘综合征的免疫生物学

Immunobiology of the critical asthma syndrome.

作者信息

Harper Richart W, Zeki Amir A

机构信息

Division of Pulmonary, Critical Care, Sleep Medicine, Department of Internal Medicine, University of California, Davis, Davis, CA, USA,

出版信息

Clin Rev Allergy Immunol. 2015 Feb;48(1):54-65. doi: 10.1007/s12016-013-8407-6.

DOI:10.1007/s12016-013-8407-6
PMID:24399247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6018052/
Abstract

It is now recognized that asthma incorporates a broad spectrum of syndromes with varying clinical manifestations. Future improvements in asthma treatment will require a clear characterization of these asthma phenotypes and the cellular mechanisms underlying these clinical manifestations. Herein, we will describe the current knowledge of asthma biology. This will include a review of the early pioneers in asthma and allergy, how this work led to our understanding of TH1 and TH2 cytokines, and the development of the "hygiene hypothesis." We will discuss the utility and limitations of the TH1-TH2 model of asthma in animal and human studies, and how this knowledge addresses controversies surrounding the hygiene hypothesis and other competing models. We will discuss novel therapies that have been developed based on mechanistic understanding of asthma pathobiology, including successes and shortcomings of these therapies. We will review the early work that led to the recognition of "asthma phenotypes." This will include the early discovery of various inflammatory subtypes in asthma and how these inflammatory subtypes correlate with response to therapy. Finally, we will describe recent discoveries in asthma biology that will include the role of the airway epithelium in asthma pathogenesis, novel cytokines important in asthma that may serve as novel therapeutic targets, and the identification of newly described innate immune cells and their role in asthma. Improved understanding of the complex biology underpinning the various asthma phenotypes is critical for our ability to optimize treatment for all patients that suffer from asthma and critical asthma syndromes.

摘要

现在人们认识到,哮喘包含一系列临床表现各异的综合征。未来哮喘治疗的改善将需要明确这些哮喘表型及其临床表现背后的细胞机制。在此,我们将描述哮喘生物学的现有知识。这将包括回顾哮喘和过敏领域的早期先驱者,他们的工作如何使我们理解TH1和TH2细胞因子,以及“卫生假说”的发展。我们将讨论哮喘的TH1 - TH2模型在动物和人体研究中的实用性和局限性,以及这些知识如何解决围绕卫生假说和其他竞争模型的争议。我们将讨论基于对哮喘病理生物学机制的理解而开发的新型疗法,包括这些疗法的成功之处和不足之处。我们将回顾导致认识到“哮喘表型”的早期工作。这将包括哮喘中各种炎症亚型的早期发现以及这些炎症亚型与治疗反应的相关性。最后,我们将描述哮喘生物学的最新发现,这将包括气道上皮在哮喘发病机制中的作用、在哮喘中起重要作用且可能成为新型治疗靶点的新型细胞因子,以及新描述的固有免疫细胞的鉴定及其在哮喘中的作用。更好地理解支撑各种哮喘表型的复杂生物学对于我们优化所有哮喘患者和严重哮喘综合征患者治疗的能力至关重要。