• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

早期呼吸道感染肺炎链球菌会加重 HDM 诱导的哮喘小鼠模型的病情。

Early-life infection of the airways with Streptococcus pneumoniae exacerbates HDM-induced asthma in a murine model.

机构信息

Department of Immunology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.

Department of Geriatrics, Second Medical Center, PLA General Hospital, Beijing, China.

出版信息

Cell Immunol. 2022 Jun;376:104536. doi: 10.1016/j.cellimm.2022.104536. Epub 2022 May 14.

DOI:10.1016/j.cellimm.2022.104536
PMID:35594699
Abstract

Respiratory tract infection early in life plays a significant role in the pathogenesis of asthma. In the present study we examine, using a murine surrogate, the effects of early life respiratory infection with Streptococcus pneumoniae (SP) on adult asthma induced by sensitisation and exposure to house dust mite (HDM) allergen. Mice (one week old) were infected with SP, then 3 weeks later sensitised to HDM emulsified with Al (OH)3 intraperitoneally and challenged intranasally with same allergen for up to a further 5 weeks to establish the asthma surrogate. Outcome measures were quantified using the FlexiVent apparatus, histology and immunohistology, ELISA and flow cytometry. The murine surrogates of asthma infected with SP early in life exhibited significantly more severe disease compared with the controls of mice without SP infection, as shown by airways responsiveness, inflammatory cellular infiltration of the airways, expression of markers of airways remodelling, serum concentrations of HDM-specific IgE and the concentrations of Th2-type cytokines and the numbers of activated Th2 and ILC2 cells in the lung tissues. These data are compatible with the hypothesis that early-life infection of the airways with SP exacerbates, at least in some individuals, subsequent HDM-induced allergic airways inflammation and associated asthma in adulthood in this murine surrogate.

摘要

生命早期的呼吸道感染在哮喘发病机制中起着重要作用。本研究通过一种小鼠替代模型,研究了生命早期呼吸道感染肺炎链球菌(SP)对尘螨(HDM)过敏原致敏和暴露引起的成年哮喘的影响。小鼠(1 周龄)用 SP 感染,然后 3 周后用 Al(OH)3 乳化的 HDM 进行腹膜内致敏,并进行多达 5 周的相同过敏原的鼻腔内攻击,以建立哮喘替代模型。使用 FlexiVent 仪器、组织学和免疫组织化学、ELISA 和流式细胞术来定量评估结果。与未感染 SP 的对照组相比,早期感染 SP 的哮喘小鼠的哮喘替代模型表现出明显更严重的疾病,表现在气道反应性、气道炎症细胞浸润、气道重塑标志物的表达、血清 HDM 特异性 IgE 浓度以及肺组织中 Th2 型细胞因子的浓度和活化 Th2 和 ILC2 细胞的数量。这些数据与以下假设一致,即生命早期 SP 对气道的感染至少在某些个体中加重了随后的 HDM 诱导的过敏性气道炎症和成年期相关哮喘。

相似文献

1
Early-life infection of the airways with Streptococcus pneumoniae exacerbates HDM-induced asthma in a murine model.早期呼吸道感染肺炎链球菌会加重 HDM 诱导的哮喘小鼠模型的病情。
Cell Immunol. 2022 Jun;376:104536. doi: 10.1016/j.cellimm.2022.104536. Epub 2022 May 14.
2
The STE20 kinase TAOK3 controls the development of house dust mite-induced asthma in mice.STE20 激酶 TAOK3 控制小鼠尘螨诱导性哮喘的发展。
J Allergy Clin Immunol. 2022 Apr;149(4):1413-1427.e2. doi: 10.1016/j.jaci.2021.08.020. Epub 2021 Sep 8.
3
Obesity Enhances Non-Th2 Airway Inflammation in a Murine Model of Allergic Asthma.肥胖增强变应性哮喘小鼠模型中非 Th2 气道炎症。
Int J Mol Sci. 2024 Jun 4;25(11):6170. doi: 10.3390/ijms25116170.
4
Lipopolysaccharide inhibits Th2 lung inflammation induced by house dust mite allergens in mice.脂多糖抑制屋尘螨变应原诱导的小鼠 Th2 肺部炎症。
Am J Respir Cell Mol Biol. 2013 Mar;48(3):382-9. doi: 10.1165/rcmb.2012-0331OC. Epub 2012 Dec 13.
5
Complement factor C5 inhibition reduces type 2 responses without affecting group 2 innate lymphoid cells in a house dust mite induced murine asthma model.补体因子 C5 抑制作用可减少 2 型反应,而不影响屋尘螨诱导的小鼠哮喘模型中的 2 类先天淋巴细胞。
Respir Res. 2019 Jul 24;20(1):165. doi: 10.1186/s12931-019-1136-5.
6
The interleukin-33 receptor ST2 is important for the development of peripheral airway hyperresponsiveness and inflammation in a house dust mite mouse model of asthma.白细胞介素-33受体ST2在哮喘的屋尘螨小鼠模型中,对于外周气道高反应性和炎症的发展至关重要。
Clin Exp Allergy. 2016 Mar;46(3):479-90. doi: 10.1111/cea.12683.
7
T cells are necessary for ILC2 activation in house dust mite-induced allergic airway inflammation in mice.在小鼠的屋尘螨诱导的过敏性气道炎症中,T细胞对于2型固有淋巴细胞(ILC2)的激活是必需的。
Eur J Immunol. 2016 Jun;46(6):1392-403. doi: 10.1002/eji.201546119. Epub 2016 May 12.
8
The absence of IL-9 reduces allergic airway inflammation by reducing ILC2, Th2 and mast cells in murine model of asthma.IL-9 的缺失通过减少哮喘小鼠模型中的 ILC2、Th2 和肥大细胞来减轻过敏性气道炎症。
BMC Pulm Med. 2022 May 6;22(1):180. doi: 10.1186/s12890-022-01976-2.
9
Development of eosinophilic inflammation is independent of B-T cell interaction in a chronic house dust mite-driven asthma model.在慢性屋尘螨诱发的哮喘模型中,嗜酸性粒细胞炎症的发展独立于B细胞与T细胞的相互作用。
Clin Exp Allergy. 2017 Apr;47(4):551-564. doi: 10.1111/cea.12834. Epub 2016 Nov 22.
10
Experimental food allergy to peanut enhances the immune response to house dust mite in the airways of mice.对花生的实验性食物过敏会增强小鼠气道中对屋尘螨的免疫反应。
Clin Exp Allergy. 2017 Jan;47(1):121-128. doi: 10.1111/cea.12799. Epub 2016 Sep 20.

引用本文的文献

1
ILC2 Diversity, Location, and Function in Pulmonary Disease.肺部疾病中2型固有淋巴细胞(ILC2)的多样性、分布位置及功能
Immunol Rev. 2025 Jul;332(1):e70036. doi: 10.1111/imr.70036.
2
Development of systemic and mucosal immune responses against gut microbiota in early life and implications for the onset of allergies.生命早期针对肠道微生物群的全身和黏膜免疫反应的发育及其对过敏发生的影响。
Front Allergy. 2024 Jul 17;5:1439303. doi: 10.3389/falgy.2024.1439303. eCollection 2024.
3
Cross-domain microbiomes: the interaction of gut, lung and environmental microbiota in asthma pathogenesis.
跨域微生物群:肠道、肺部和环境微生物群在哮喘发病机制中的相互作用
Front Nutr. 2024 Jun 21;11:1346923. doi: 10.3389/fnut.2024.1346923. eCollection 2024.
4
Early exposure to infections increases the risk of allergic rhinitis-a systematic review and meta-analysis.早期接触感染会增加过敏性鼻炎的风险——系统评价和荟萃分析。
BMC Pediatr. 2023 Mar 1;23(1):96. doi: 10.1186/s12887-023-03870-0.
5
Microbial dysbiosis and childhood asthma development: Integrated role of the airway and gut microbiome, environmental exposures, and host metabolic and immune response.微生物失调与儿童哮喘发病机制:气道和肠道微生物组、环境暴露以及宿主代谢和免疫反应的综合作用
Front Immunol. 2022 Sep 30;13:1028209. doi: 10.3389/fimmu.2022.1028209. eCollection 2022.