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重症支气管哮喘抗体治疗的进展与挑战

Advances and Challenges of Antibody Therapeutics for Severe Bronchial Asthma.

作者信息

Abe Yuko, Suga Yasuhiko, Fukushima Kiyoharu, Ohata Hayase, Niitsu Takayuki, Nabeshima Hiroshi, Nagahama Yasuharu, Kida Hiroshi, Kumanogoh Atsushi

机构信息

Department of Respiratory Medicine and Clinical Immunology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan.

Laboratory of Host Defense, World Premier Institute Immunology Frontier Research Center (WPI-IFReC), Osaka University, Osaka 565-0871, Japan.

出版信息

Int J Mol Sci. 2021 Dec 22;23(1):83. doi: 10.3390/ijms23010083.

DOI:10.3390/ijms23010083
PMID:35008504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8744863/
Abstract

Asthma is a disease that consists of three main components: airway inflammation, airway hyperresponsiveness, and airway remodeling. Persistent airway inflammation leads to the destruction and degeneration of normal airway tissues, resulting in thickening of the airway wall, decreased reversibility, and increased airway hyperresponsiveness. The progression of irreversible airway narrowing and the associated increase in airway hyperresponsiveness are major factors in severe asthma. This has led to the identification of effective pharmacological targets and the recognition of several biomarkers that enable a more personalized approach to asthma. However, the efficacies of current antibody therapeutics and biomarkers are still unsatisfactory in clinical practice. The establishment of an ideal phenotype classification that will predict the response of antibody treatment is urgently needed. Here, we review recent advancements in antibody therapeutics and novel findings related to the disease process for severe asthma.

摘要

哮喘是一种由三个主要成分组成的疾病

气道炎症、气道高反应性和气道重塑。持续性气道炎症会导致正常气道组织的破坏和退化,导致气道壁增厚、可逆性降低以及气道高反应性增加。不可逆性气道狭窄的进展以及相关的气道高反应性增加是重度哮喘的主要因素。这导致了有效药理靶点的确定以及几种生物标志物的识别,从而能够对哮喘采取更个性化的治疗方法。然而,目前抗体疗法和生物标志物的疗效在临床实践中仍不尽人意。迫切需要建立一种理想的表型分类来预测抗体治疗的反应。在此,我们综述了抗体疗法的最新进展以及与重度哮喘疾病过程相关的新发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/8744863/963a71816988/ijms-23-00083-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/8744863/1934e1718fc7/ijms-23-00083-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/8744863/29789991681b/ijms-23-00083-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/8744863/963a71816988/ijms-23-00083-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/8744863/1934e1718fc7/ijms-23-00083-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/8744863/29789991681b/ijms-23-00083-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed4/8744863/963a71816988/ijms-23-00083-g003.jpg

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2
Novel insights into the pathogenesis of lung fibrosis: the RBM7-NEAT1-CXCL12-SatM axis at fibrosis onset.新型肺纤维化发病机制研究进展:纤维化起始时的 RBM7-NEAT1-CXCL12-SatM 轴。
Int Immunol. 2021 Nov 25;33(12):659-663. doi: 10.1093/intimm/dxab034.
3
Impact of baseline clinical asthma characteristics on the response to mepolizumab: a post hoc meta-analysis of two Phase III trials.
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Front Pharmacol. 2025 Jan 20;15:1510806. doi: 10.3389/fphar.2024.1510806. eCollection 2024.
4
A Review on Asthma and Allergy: Current Understanding on Molecular Perspectives.哮喘与过敏综述:分子视角的当前认识
J Clin Med. 2024 Sep 27;13(19):5775. doi: 10.3390/jcm13195775.
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Ther Adv Respir Dis. 2023 Jan-Dec;17:17534666231213637. doi: 10.1177/17534666231213637.
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J Asthma Allergy. 2023 Jan 4;16:9-21. doi: 10.2147/JAA.S375325. eCollection 2023.
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