中文版 | English
名称

Prevention of IL-6 signaling ameliorates toluene diisocyanate-induced steroid-resistant asthma

作者
发布日期
2022
关键词
语种
英语
相关链接[来源记录]
资助项目
China Postdoctoral Science Foundation["2021M691243","2020M673082"]
摘要
["Background: Accumulating evidence indicated the crucial role for interleukin 6 (IL-6) signaling in the development of allergic asthma. Yet, the role of IL-6 signaling in toluene diisocyanate (TDI)-induced mixed granulocytic airway inflammation still remains unclear. Thus, the aims of this study were to dissect the role of IL-6 signaling and to evaluate the effect of tocilizumab on TDI-induced steroidresistant asthma.","Methods: TDI-induced asthma model was prepared and asthmatic mice were respectively given IL-6 monoclonal antibody, IL-6R monoclonal antibody (tocilizumab, 5 mg/kg, i.p. after each challenge) for therapeutic purposes or isotype IgG as control.","Results: TDI exposure just elevated IL-6R expression in the infiltrated inflammatory cells around the airway, but increased glycoprotein 130 expression in the whole lung, especially in bronchial epithelium. Moreover, TDI inhalation increased airway hyperresponsiveness (AHR) to methacholine, coupled with mixed granulocytic inflammation, exaggerated epithelial denudation, airway smooth muscle thickening, goblet cell metaplasia, extensive submucosal collagen deposition, dysregulated Th2/Th17 responses, as well as innate immune responses and raised serum IgE. And almost all these responses except for raised serum IgE were markedly ameliorated by the administration of IL-6 neutralizing antibody or tocilizumab, but exhibited poor response to systemic steroid treatment. Also, TDI challenge induced nucleocytoplasm translocation of HMGB1 and promoted its release in the BALF, as well as elevated lung level of STAT3 phosphorylation, which were inhibited by anti-IL-6 and anti-IL-6R treatment.","Conclusions: Our data suggested that IL-6 monoclonal antibody and tocilizumab might effectively abrogate TDI-induced airway inflammation and remodeling, which could be used as a clinical potential therapy for patients with severe asthma. Copyright (c) 2021, Japanese Society of Allergology. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)."]
DOI
期刊来源
卷号
71
期号
1
出版者
出版地
MY BLDG 4F, 1-13-3, UENO, TAITO-KU, TOKYO, 110-0005, JAPAN
ISSN
1323-8930
收录类别
学校署名
第一 ; 通讯
来源库
Web of Science
通讯作者Liu, Shengming; Chen, Rongchang
WOS记录号
WOS:000892843800010
WOS类目
Allergy ; Immunology
WOS研究方向
Allergy ; Immunology
EISSN
1440-1592
ESI学科分类
IMMUNOLOGY
引用统计
被引频次[WOS]:0
成果类型其他
条目标识符http://sustech.caswiz.com/handle/2SGJ60CL/417083
专题南方科技大学第一附属医院
作者单位
1.Southern Univ Sci & Technol, Shenzhen Peoples Hosp, Affiliated Hosp 1,Clinical Med Coll 2, Jinan Univ,Shenzhen Inst Resp Dis,Dept Pulm & Cri, Shenzhen, Peoples R China
2.Jinan Univ, Dept Pulm & Crit Care Med, Affiliated Hosp 1, Guangzhou, Peoples R China
3.Beijing Univ Chinese Med, Shenzhen Hosp, Dept Clin Lab, Shenzhen, Peoples R China
4.Guangzhou Med Univ, Affiliated Hosp 1, Guangzhou Inst Resp Hlth, State Key Lab Resp Dis, Guangzhou, Peoples R China
第一作者单位南方科技大学第一附属医院
通讯作者单位南方科技大学第一附属医院
推荐引用方式
GB/T 7714
Chen, Shuyu,Chen, Zhuoyu,Deng, Yao,et al. Prevention of IL-6 signaling ameliorates toluene diisocyanate-induced steroid-resistant asthma. 2022-01-01.
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