• 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

肺部局部白细胞介素-4的表达会降低肺部流感病毒特异性继发性细胞毒性T细胞反应。

Local IL-4 expression in the lung reduces pulmonary influenza-virus-specific secondary cytotoxic T cell responses.

作者信息

Bot A, Holz A, Christen U, Wolfe T, Temann A, Flavell R, von Herrath M

机构信息

Department of Neuropharmacology, Division of Virology, IMM6, The Scripps Research Institute, La Jolla, CA 92037, USA.

出版信息

Virology. 2000 Mar 30;269(1):66-77. doi: 10.1006/viro.2000.0187.

DOI:10.1006/viro.2000.0187
PMID:10725199
Abstract

We studied the effect of lung-specific IL-4 expression on the T cell response during primary and secondary heterologous infection with influenza virus by using transgenic mice that express IL-4 under a lung-specific promoter. Subsequent to primary infection with a type A/H1N1 influenza virus these transgenic mice exhibited similar local recruitment of CD4(+) and CD8(+) T cells and only slightly decreased virus-specific CTL activity. However, during secondary challenge with a heterologous influenza virus, the local infiltration with virus-specific, MHC class I-restricted CD8(+) T cells was significantly decreased compared to that of nontransgenic littermates. The ability of IL-4 transgenic mice to clear the heterologous infection was delayed but not abrogated. This was associated with a faster virus-neutralizing antibody response in IL-4 transgenic mice and with their ability to mount significant Th1 responses even in the presence of increased local IL-4 expression. Our observations demonstrate a negative regulatory effect of IL-4 on memory Tc1/CD8(+) T cells, but are also consistent with complementary mechanisms important for virus clearance such as virus-neutralizing antibodies. The reduction of memory CTL in the presence of IL-4 might have consequences for understanding the course of influenza infection in situations where T(H)2 immunity is increased.

摘要

我们利用在肺特异性启动子控制下表达白细胞介素4(IL-4)的转基因小鼠,研究了肺特异性IL-4表达在甲型流感病毒初次和二次异源感染期间对T细胞应答的影响。在用A/H1N1甲型流感病毒进行初次感染后,这些转基因小鼠表现出相似的CD4(+)和CD8(+) T细胞局部募集,且病毒特异性CTL活性仅略有降低。然而,在异源流感病毒二次攻击期间,与非转基因同窝小鼠相比,病毒特异性、MHC I类限制性CD8(+) T细胞的局部浸润显著减少。IL-4转基因小鼠清除异源感染的能力延迟但未被消除。这与IL-4转基因小鼠中更快的病毒中和抗体应答以及它们即使在局部IL-4表达增加的情况下仍能产生显著Th1应答的能力有关。我们的观察结果证明了IL-4对记忆性Tc1/CD8(+) T细胞具有负调节作用,但也与病毒清除的重要互补机制如病毒中和抗体一致。在IL-4存在的情况下记忆性CTL的减少可能对理解T(H)2免疫增强情况下流感感染的病程具有重要意义。

相似文献

1
Local IL-4 expression in the lung reduces pulmonary influenza-virus-specific secondary cytotoxic T cell responses.肺部局部白细胞介素-4的表达会降低肺部流感病毒特异性继发性细胞毒性T细胞反应。
Virology. 2000 Mar 30;269(1):66-77. doi: 10.1006/viro.2000.0187.
2
Mice can recover from pulmonary influenza virus infection in the absence of class I-restricted cytotoxic T cells.在缺乏I类限制性细胞毒性T细胞的情况下,小鼠可以从肺部流感病毒感染中恢复。
J Immunol. 1992 Jan 1;148(1):212-7.
3
Expression of interleukin-4 by recombinant respiratory syncytial virus is associated with accelerated inflammation and a nonfunctional cytotoxic T-lymphocyte response following primary infection but not following challenge with wild-type virus.重组呼吸道合胞病毒表达白细胞介素-4与初次感染后炎症加速和细胞毒性T淋巴细胞反应无功能有关,但在野生型病毒攻击后则不然。
J Virol. 2005 Aug;79(15):9515-26. doi: 10.1128/JVI.79.15.9515-9526.2005.
4
Do L3T4+ T cells act as effector cells in protection against influenza virus infection.L3T4+ T细胞在抵抗流感病毒感染的过程中是否作为效应细胞发挥作用?
Immunology. 1987 Sep;62(1):139-44.
5
Naive, effector, and memory CD8 T cells in protection against pulmonary influenza virus infection: homing properties rather than initial frequencies are crucial.初始、效应和记忆性CD8 T细胞在抵抗肺部流感病毒感染中的作用:归巢特性而非初始频率至关重要。
J Immunol. 1999 Nov 15;163(10):5535-43.
6
Quantitative analysis of the influenza virus-specific CD4+ T cell memory in the absence of B cells and Ig.在缺乏B细胞和免疫球蛋白的情况下,对流感病毒特异性CD4+T细胞记忆进行定量分析。
J Immunol. 1996 Oct 1;157(7):2947-52.
7
Strong memory CD8+ T cell responses against immunodominant and three new subdominant HLA-B27-restricted influenza A CTL epitopes following secondary infection of HLA-B27 transgenic mice.HLA - B27转基因小鼠二次感染后,针对免疫显性和三个新的亚显性HLA - B27限制性甲型流感CTL表位产生的强烈记忆性CD8 + T细胞应答。
Cell Immunol. 2005 Apr;234(2):110-23. doi: 10.1016/j.cellimm.2005.06.004.
8
Complement component C3 promotes T-cell priming and lung migration to control acute influenza virus infection.补体成分C3促进T细胞启动和向肺部迁移以控制急性流感病毒感染。
Nat Med. 2002 Apr;8(4):373-8. doi: 10.1038/nm0402-373.
9
CC chemokine receptor 7 expression by effector/memory CD4+ T cells depends on antigen specificity and tissue localization during influenza A virus infection.在甲型流感病毒感染期间,效应/记忆CD4+ T细胞对CC趋化因子受体7的表达取决于抗原特异性和组织定位。
J Virol. 2004 Jul;78(14):7528-35. doi: 10.1128/JVI.78.14.7528-7535.2004.
10
Interleukin-1 is responsible for acute lung immunopathology but increases survival of respiratory influenza virus infection.白细胞介素-1 是急性肺免疫病理学的病因,但可提高呼吸道流感病毒感染后的生存率。
J Virol. 2005 May;79(10):6441-8. doi: 10.1128/JVI.79.10.6441-6448.2005.

引用本文的文献

1
Influence of SARS-COV-2 Infection on Cytokine Production by Mitogen-Stimulated Peripheral Blood Mononuclear Cells and Neutrophils in COVID-19 Intensive Care Unit Patients.新型冠状病毒肺炎重症监护病房患者中,严重急性呼吸综合征冠状病毒2感染对丝裂原刺激的外周血单个核细胞和中性粒细胞产生细胞因子的影响
Microorganisms. 2022 Nov 4;10(11):2194. doi: 10.3390/microorganisms10112194.
2
Specific Cytokine Profiles Predict the Severity of Influenza A Pneumonia: A Prospectively Multicenter Pilot Study.特定细胞因子谱可预测甲型流感肺炎的严重程度:一项前瞻性多中心初步研究。
Biomed Res Int. 2021 Oct 13;2021:9533044. doi: 10.1155/2021/9533044. eCollection 2021.
3
Inflammatory Mechanisms in COVID-19 and Atherosclerosis: Current Pharmaceutical Perspectives.
新型冠状病毒肺炎与动脉粥样硬化的炎症机制:当前药物治疗观点。
Int J Mol Sci. 2021 Jun 21;22(12):6607. doi: 10.3390/ijms22126607.
4
IL-6 and IL-10 as predictors of disease severity in COVID-19 patients: results from meta-analysis and regression.IL-6和IL-10作为COVID-19患者疾病严重程度的预测指标:荟萃分析和回归结果
Heliyon. 2021 Feb;7(2):e06155. doi: 10.1016/j.heliyon.2021.e06155. Epub 2021 Jan 29.
5
SARS-CoV-2 infection: The role of cytokines in COVID-19 disease.严重急性呼吸综合征冠状病毒 2 感染:细胞因子在 COVID-19 疾病中的作用。
Cytokine Growth Factor Rev. 2020 Aug;54:62-75. doi: 10.1016/j.cytogfr.2020.06.001. Epub 2020 Jun 2.
6
More Than Just a Barrier: The Immune Functions of the Airway Epithelium in Asthma Pathogenesis.不仅仅是一道屏障:气道上皮在哮喘发病机制中的免疫功能。
Front Immunol. 2020 Apr 28;11:761. doi: 10.3389/fimmu.2020.00761. eCollection 2020.
7
Stable incorporation of GM-CSF into dissolvable microneedle patch improves skin vaccination against influenza.GM-CSF 的稳定掺入可溶解微针贴片可改善流感的皮肤疫苗接种效果。
J Control Release. 2018 Apr 28;276:1-16. doi: 10.1016/j.jconrel.2018.02.033. Epub 2018 Feb 26.
8
IL-4: an important cytokine in determining the fate of T cells.白细胞介素-4:决定T细胞命运的一种重要细胞因子。
Biophys Rev. 2014 Mar;6(1):111-118. doi: 10.1007/s12551-013-0133-z. Epub 2014 Jan 9.
9
Differential Immune Profiles in Two Pandemic Influenza A(H1N1)pdm09 Virus Waves at Pandemic Epicenter.大流行中心两次甲型H1N1流感大流行病毒浪潮中的差异免疫特征。
Arch Med Res. 2015 Nov;46(8):651-8. doi: 10.1016/j.arcmed.2015.12.003. Epub 2015 Dec 13.
10
CD206+ cell number differentiates influenza A (H1N1)pdm09 from seasonal influenza A virus in fatal cases.在致命病例中,CD206+细胞数量可区分甲型H1N1pdm09流感与季节性甲型流感病毒。
Mediators Inflamm. 2014;2014:921054. doi: 10.1155/2014/921054. Epub 2014 Nov 25.