• 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

老年大鼠在气道过敏性炎症中嗜酸性粒细胞积聚失败。

Failure of aged rats to accumulate eosinophils in allergic inflammation of the airway.

作者信息

Yagi T, Sato A, Hayakawa H, Ide K

机构信息

Second Department of Internal Medicine, Hamamatsu University School of Medicine, Japan.

出版信息

J Allergy Clin Immunol. 1997 Jan;99(1 Pt 1):38-47. doi: 10.1016/s0091-6749(97)70298-7.

DOI:10.1016/s0091-6749(97)70298-7
PMID:9003209
Abstract

To investigate the effect of aging on the allergic airway response, we examined the bronchoconstrictive responses and cellular inflammatory changes in a rat model of bronchial asthma by evaluating young and old animals. Two different age groups of Brown-Norway rats, actively sensitized by injection of ovalbumin into the foot pads, were used: 7 to 8 weeks old (young group) and 100 to 120 weeks old (aged group). Both the aged and young rats produced on ovalbumin-specific IgE antibody and exhibited an immediate asthmatic response after exposure to ovalbumin, but the degree of specific IgE antibody was significantly higher in young rats. The young group showed a marked increase in the number of eosinophils and neutrophils in bronchoalveolar lavage fluid 2 days after exposure to ovalbumin, whereas no eosinophilia was seen in the aged group. To evaluate the mechanism of the decreased accumulation of eosinophils in aged rats, cells from popliteal lymph nodes from ovalbumin-sensitized rats were incubated with ovalbumin for 48 hours. Although eosinophil chemotactic activity, determined by a modified Boyden chamber method, was present in the supernatant of cultured lymph node cells from young rats, it was absent from those of aged rats. In vivo administration of anti-IL-5 monoclonal antibody revealed that one of the factors of eosinophil chemotactic activity was IL-5. Lymph node cells from aged rats tended to produce greater amounts of interferon-gamma than did those from young animals. Findings indicate that aged rats have a defect in eosinophil accumulation in sites exposed to antigen, probably because of an age-dependent alteration in T cells.

摘要

为研究衰老对过敏性气道反应的影响,我们通过评估年轻和老年动物,检测了支气管哮喘大鼠模型中的支气管收缩反应和细胞炎症变化。使用了两组不同年龄的经足垫注射卵清蛋白主动致敏的Brown-Norway大鼠:7至8周龄(年轻组)和100至120周龄(老年组)。老年和年轻大鼠均产生了卵清蛋白特异性IgE抗体,并在接触卵清蛋白后表现出即刻哮喘反应,但年轻大鼠的特异性IgE抗体水平显著更高。年轻组在接触卵清蛋白2天后,支气管肺泡灌洗液中的嗜酸性粒细胞和中性粒细胞数量显著增加,而老年组未见嗜酸性粒细胞增多。为评估老年大鼠嗜酸性粒细胞积聚减少的机制,将来自卵清蛋白致敏大鼠腘窝淋巴结的细胞与卵清蛋白孵育48小时。尽管通过改良的Boyden小室法测定,年轻大鼠培养的淋巴结细胞上清液中存在嗜酸性粒细胞趋化活性,但老年大鼠的上清液中未检测到。体内给予抗IL-5单克隆抗体表明,嗜酸性粒细胞趋化活性的因素之一是IL-5。老年大鼠的淋巴结细胞比年轻动物的淋巴结细胞倾向于产生更多的干扰素-γ。研究结果表明,老年大鼠在抗原暴露部位的嗜酸性粒细胞积聚存在缺陷,这可能是由于T细胞的年龄依赖性改变所致。

相似文献

1
Failure of aged rats to accumulate eosinophils in allergic inflammation of the airway.老年大鼠在气道过敏性炎症中嗜酸性粒细胞积聚失败。
J Allergy Clin Immunol. 1997 Jan;99(1 Pt 1):38-47. doi: 10.1016/s0091-6749(97)70298-7.
2
Adoptive transfer of allergic airway responses with sensitized lymphocytes in BN rats.在BN大鼠中通过致敏淋巴细胞进行变应性气道反应的过继转移。
Am J Respir Crit Care Med. 1995 Jul;152(1):64-70. doi: 10.1164/ajrccm.152.1.7599864.
3
Marked airway eosinophilia prevents development of airway hyper-responsiveness during an allergic response in IL-5 transgenic mice.在白细胞介素-5转基因小鼠的过敏反应过程中,显著的气道嗜酸性粒细胞增多可阻止气道高反应性的发展。
J Immunol. 2003 Jun 1;170(11):5756-63. doi: 10.4049/jimmunol.170.11.5756.
4
Transfer of allergic airway responses with antigen-primed CD4+ but not CD8+ T cells in brown Norway rats.在棕色挪威大鼠中,抗原致敏的CD4 +而非CD8 + T细胞介导变应性气道反应的转移。
J Clin Invest. 1995 Sep;96(3):1303-10. doi: 10.1172/JCI118165.
5
Effect of diesel exhaust particles on allergic reactions and airway responsiveness in ovalbumin-sensitized brown Norway rats.柴油尾气颗粒对卵清蛋白致敏的棕色挪威大鼠过敏反应和气道反应性的影响。
Toxicol Sci. 2005 Nov;88(1):202-12. doi: 10.1093/toxsci/kfi280. Epub 2005 Aug 17.
6
Exposure of brown Norway rats to diesel exhaust particles prior to ovalbumin (OVA) sensitization elicits IgE adjuvant activity but attenuates OVA-induced airway inflammation.在对卵清蛋白(OVA)致敏之前,将棕色挪威大鼠暴露于柴油废气颗粒会引发IgE佐剂活性,但会减轻OVA诱导的气道炎症。
Toxicol Sci. 2005 Nov;88(1):150-60. doi: 10.1093/toxsci/kfi298. Epub 2005 Aug 24.
7
Effect of CD8+ T-cell depletion on bronchial hyper-responsiveness and inflammation in sensitized and allergen-exposed Brown-Norway rats.CD8 + T细胞耗竭对致敏和暴露于变应原的Brown-Norway大鼠支气管高反应性和炎症的影响。
Immunology. 1999 Mar;96(3):416-23. doi: 10.1046/j.1365-2567.1999.00699.x.
8
Role of very late activation antigen-4 in the antigen-induced accumulation of eosinophils and lymphocytes in the lungs and airway lumen of sensitized brown Norway rats.极晚期活化抗原-4在致敏棕色挪威大鼠肺部和气道腔内抗原诱导的嗜酸性粒细胞和淋巴细胞聚集中的作用。
Am J Respir Cell Mol Biol. 1996 Aug;15(2):172-83. doi: 10.1165/ajrcmb.15.2.8703473.
9
Inhibitory effects of endogenous and exogenous interferon-gamma on bronchial hyperresponsiveness, allergic inflammation and T-helper 2 cytokines in Brown-Norway rats.内源性和外源性干扰素-γ对棕色挪威大鼠支气管高反应性、变应性炎症和辅助性T细胞2细胞因子的抑制作用
Immunology. 1999 Oct;98(2):280-8. doi: 10.1046/j.1365-2567.1999.00870.x.
10
Effect of ageing on pulmonary inflammation, airway hyperresponsiveness and T and B cell responses in antigen-sensitized and -challenged mice.衰老对抗原致敏和激发小鼠肺部炎症、气道高反应性以及T细胞和B细胞反应的影响。
Clin Exp Allergy. 2007 Sep;37(9):1392-403. doi: 10.1111/j.1365-2222.2007.02775.x.

引用本文的文献

1
Interconnections between Inflammageing and Immunosenescence during Ageing.衰老过程中炎症与免疫衰老的相互关系。
Cells. 2022 Jan 21;11(3):359. doi: 10.3390/cells11030359.
2
Short palate, lung, and nasal epithelial clone 1 (SPLUNC1) level determines steroid-resistant airway inflammation in aging.短 palate、lung、和鼻腔上皮克隆 1(SPLUNC1)水平决定了衰老中类固醇抵抗性气道炎症。
Am J Physiol Lung Cell Mol Physiol. 2022 Jan 1;322(1):L102-L115. doi: 10.1152/ajplung.00315.2021. Epub 2021 Dec 1.
3
Senescence in Pulmonary Fibrosis: Between Aging and Exposure.
肺纤维化中的衰老:介于衰老与暴露之间
Front Med (Lausanne). 2020 Nov 12;7:606462. doi: 10.3389/fmed.2020.606462. eCollection 2020.
4
In utero exposure to genistein decreased intranasal house dust mite-induced respiratory allergy in middle-aged male B6C3F1 offspring.子宫内暴露于染料木黄酮可降低中年雄性 B6C3F1 后代经鼻室内尘螨诱发的呼吸道过敏。
Toxicol Lett. 2020 Oct 15;333:222-231. doi: 10.1016/j.toxlet.2020.07.013. Epub 2020 Aug 13.
5
In Utero exposure to genistein enhanced intranasal house dust mite allergen-induced respiratory sensitization in young adult B6C3F1 mice.子宫内暴露于染料木黄酮会增强年轻成年B6C3F1小鼠鼻内屋尘螨过敏原诱导的呼吸道致敏作用。
Toxicol Lett. 2016 Jun 24;253:17-26. doi: 10.1016/j.toxlet.2016.04.017. Epub 2016 Apr 22.
6
Changes in IgE sensitization and total IgE levels over 20 years of follow-up.20年随访期间IgE致敏和总IgE水平的变化。
J Allergy Clin Immunol. 2016 Jun;137(6):1788-1795.e9. doi: 10.1016/j.jaci.2015.09.037. Epub 2015 Nov 14.
7
Changes in immune function in asthma in the elderly.老年人哮喘患者免疫功能的变化
Aging health. 2009 Sep;5(4):551-559. doi: 10.2217/ahe.09.47.
8
Asthma in the elderly: Current understanding and future research needs--a report of a National Institute on Aging (NIA) workshop.老年人哮喘:当前的认识和未来的研究需求——美国国家老龄化研究所(NIA)研讨会的报告。
J Allergy Clin Immunol. 2011 Sep;128(3 Suppl):S4-24. doi: 10.1016/j.jaci.2011.06.048.
9
Leukocyte function in the aging immune system.白细胞在衰老免疫系统中的功能。
J Leukoc Biol. 2010 Jun;87(6):1001-9. doi: 10.1189/jlb.0809542. Epub 2010 Mar 3.
10
Innate immunity and aging.先天免疫与衰老
Exp Gerontol. 2008 Aug;43(8):718-28. doi: 10.1016/j.exger.2008.05.016. Epub 2008 Jun 11.