Endotypic heterogeneity and pathogenesis in chronic rhinosinusitis

被引:3
作者
Bai, Junqin [1 ]
Tan, Bruce K. [1 ,2 ]
Kato, Atsushi [1 ,2 ,3 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Otolaryngol, Chicago, IL USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Med, Div Allergy & Immunol, Chicago, IL USA
[3] Northwestern Univ, Feinberg Sch Med, Div Allergy & Immunol, 240 E Huron St,Room M304, Chicago, IL 60611 USA
关键词
biologics; chronic rhinosinusitis; endotype; epithelial remodeling; pathogenesis; INNATE LYMPHOID-CELLS; THYMIC STROMAL LYMPHOPOIETIN; NASAL POLYPS; INCREASED EXPRESSION; EPITHELIAL-CELLS; ONCOSTATIN M; TSLP EXPRESSION; B-CELLS; INFLAMMATION; TISSUE;
D O I
10.1097/ACI.0000000000000954
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Purpose of review This review aims to provide updates in realms of endotypic heterogeneity, pathogenesis at the molecular level, potential of biomarkers, and cutting-edge scope of biologics in CRS. Recent findings High-dimensional analyses, such as transcriptomes, and machine learning, have significantly enhanced CRS endotyping, uncovering diverse pathogenetic mechanisms contributing to its heterogeneity. The dynamic process of epithelial remodeling in CRS pathogenesis has gained more clarity and support as exemplified by IL-13 and oncostatin M (OSM) that are shown intricately linked to epithelial barrier dysfunction. Moreover, anti-dsDNA autoantibody, BAFF, periostin, and cystatin SN show promise as potentials biomarkers, offering diagnostic and prognostic value for CRS. Summary The identification of inflammatory molecules involved in endotype specific signaling pathways provides insights into the underlying mechanisms and verifiable biomarkers for diagnosis and prediction of disease severity. More comprehensive clinical studies should be conducted to facilitate biologics from bench to bedside in treating CRS. Copyright (C) 2023 Wolters Kluwer Health, Inc. All rights reserved.
引用
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页码:1 / 8
页数:8
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