• 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

2009年甲型H1N1流感大流行病毒实验性感染猪后自然杀伤细胞的早期反应

Early responses of natural killer cells in pigs experimentally infected with 2009 pandemic H1N1 influenza A virus.

作者信息

Forberg Hilde, Hauge Anna G, Valheim Mette, Garcon Fanny, Nunez Alejandro, Gerner Wilhelm, Mair Kerstin H, Graham Simon P, Brookes Sharon M, Storset Anne K

机构信息

Department of Laboratory Services, Norwegian Veterinary Institute, Oslo, Norway.

Virology Department, Animal Health and Veterinary Laboratories Agency, Addlestone, United Kingdom.

出版信息

PLoS One. 2014 Jun 23;9(6):e100619. doi: 10.1371/journal.pone.0100619. eCollection 2014.

DOI:10.1371/journal.pone.0100619
PMID:24955764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4067341/
Abstract

Natural killer (NK) cells are important players in the innate immune response against influenza A virus and the activating receptor NKp46, which binds hemagglutinin on the surface of infected cells, has been assigned a role in this context. As pigs are natural hosts for influenza A viruses and pigs possess both NKp46- and NKp46+ NK cells, they represent a good animal model for studying the role of the NKp46 receptor during influenza. We explored the role of NK cells in piglets experimentally infected with 2009 pandemic H1N1 influenza virus by flow cytometric analyses of cells isolated from blood and lung tissue and by immunostaining of lung tissue sections. The number of NKp46+ NK cells was reduced while NKp46- NK cells remained unaltered in the blood 1-3 days after infection. In the lungs, the intensity of NKp46 expression on NK cells was increased during the first 3 days, and areas where influenza virus nucleoprotein was detected were associated with increased numbers of NKp46+ NK cells when compared to uninfected areas. NKp46+ NK cells in the lung were neither found to be infected with influenza virus nor to be undergoing apoptosis. The binding of porcine NKp46 to influenza virus infected cells was verified in an in vitro assay. These data support the involvement of porcine NKp46+ NK cells in the local immune response against influenza virus.

摘要

自然杀伤(NK)细胞是甲型流感病毒天然免疫反应中的重要参与者,在这种情况下,与感染细胞表面血凝素结合的激活受体NKp46发挥了作用。由于猪是甲型流感病毒的天然宿主,且猪同时拥有NKp46 - 和NKp46 + NK细胞,它们是研究NKp46受体在流感期间作用的良好动物模型。我们通过对从血液和肺组织中分离的细胞进行流式细胞术分析以及对肺组织切片进行免疫染色,探讨了NK细胞在实验感染2009年大流行H1N1流感病毒的仔猪中的作用。感染后1 - 3天,血液中NKp46 + NK细胞数量减少,而NKp46 - NK细胞数量保持不变。在肺中,NK细胞上NKp46表达强度在最初3天增加,与未感染区域相比,检测到流感病毒核蛋白的区域NKp46 + NK细胞数量增加。肺中的NKp46 + NK细胞既未被发现感染流感病毒,也未发生凋亡。体外试验证实了猪NKp46与流感病毒感染细胞的结合。这些数据支持猪NKp46 + NK细胞参与针对流感病毒的局部免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/4e765df1f055/pone.0100619.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/080a8e86910a/pone.0100619.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/4c72abbe7d59/pone.0100619.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/01205d17de74/pone.0100619.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/6afb7a7f447b/pone.0100619.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/dfbfe59537ce/pone.0100619.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/bb391abfd4ef/pone.0100619.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/4e765df1f055/pone.0100619.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/080a8e86910a/pone.0100619.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/4c72abbe7d59/pone.0100619.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/01205d17de74/pone.0100619.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/6afb7a7f447b/pone.0100619.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/dfbfe59537ce/pone.0100619.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/bb391abfd4ef/pone.0100619.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2c2/4067341/4e765df1f055/pone.0100619.g007.jpg

相似文献

1
Early responses of natural killer cells in pigs experimentally infected with 2009 pandemic H1N1 influenza A virus.2009年甲型H1N1流感大流行病毒实验性感染猪后自然杀伤细胞的早期反应
PLoS One. 2014 Jun 23;9(6):e100619. doi: 10.1371/journal.pone.0100619. eCollection 2014.
2
Killing of avian and Swine influenza virus by natural killer cells.自然杀伤细胞对禽源和猪源流感病毒的杀伤作用。
J Virol. 2010 Apr;84(8):3993-4001. doi: 10.1128/JVI.02289-09. Epub 2010 Feb 3.
3
Phenotypic and Functional Characteristics of a Novel Influenza Virus Hemagglutinin-Specific Memory NK Cell.一种新型流感病毒血凝素特异性记忆性自然杀伤细胞的表型和功能特征
J Virol. 2021 May 24;95(12). doi: 10.1128/JVI.00165-21.
4
Expansion of 2B4+ natural killer (NK) cells and decrease in NKp46+ NK cells in response to influenza.2B4+ 自然杀伤 (NK) 细胞扩增和 NKp46+ NK 细胞减少对流感的反应。
Immunology. 2011 Apr;132(4):516-26. doi: 10.1111/j.1365-2567.2010.03394.x. Epub 2011 Jan 7.
5
Differential activation of NK cells by influenza A pseudotype H5N1 and 1918 and 2009 pandemic H1N1 viruses.甲型流感 H5N1 假型病毒、1918 年和 2009 年大流行 H1N1 病毒对 NK 细胞的差异激活。
J Virol. 2010 Aug;84(15):7822-31. doi: 10.1128/JVI.00069-10. Epub 2010 May 19.
6
Neuraminidase-mediated, NKp46-dependent immune-evasion mechanism of influenza viruses.神经氨酸酶介导的、NKp46 依赖性的流感病毒免疫逃逸机制。
Cell Rep. 2013 Apr 25;3(4):1044-50. doi: 10.1016/j.celrep.2013.03.034. Epub 2013 Apr 18.
7
Altered NKp46 Recognition and Elimination of Influenza B Viruses.改变的 NKp46 识别和流感 B 病毒的消除。
Viruses. 2020 Dec 27;13(1):34. doi: 10.3390/v13010034.
8
Red ginseng and vitamin C increase immune cell activity and decrease lung inflammation induced by influenza A virus/H1N1 infection.红参和维生素C可增强免疫细胞活性,并减轻甲型流感病毒/H1N1感染所致的肺部炎症。
J Pharm Pharmacol. 2016 Mar;68(3):406-20. doi: 10.1111/jphp.12529. Epub 2016 Feb 21.
9
Inhibition of human natural killer cell activity by influenza virions and hemagglutinin.流感病毒及其血凝素对人自然杀伤细胞活性的抑制作用。
J Virol. 2010 May;84(9):4148-57. doi: 10.1128/JVI.02340-09. Epub 2010 Feb 17.
10
NK cells exacerbate the pathology of influenza virus infection in mice.NK 细胞加剧了流感病毒感染小鼠的病理过程。
Eur J Immunol. 2013 Apr;43(4):929-38. doi: 10.1002/eji.201242620. Epub 2013 Mar 6.

引用本文的文献

1
Regulation of pulmonary plasma cell responses during secondary infection with influenza virus.流感病毒二次感染期间肺浆细胞反应的调节
J Exp Med. 2024 Jul 1;221(7). doi: 10.1084/jem.20232014. Epub 2024 Apr 25.
2
From Snoot to Tail: A Brief Review of Influenza Virus Infection and Immunity in Pigs.从头至尾:猪流感病毒感染与免疫简述。
J Immunol. 2023 Oct 15;211(8):1187-1194. doi: 10.4049/jimmunol.2300385.
3
Simultaneous co-infection with swine influenza A and porcine reproductive and respiratory syndrome viruses potentiates adaptive immune responses.

本文引用的文献

1
Studying immunity to zoonotic diseases in the natural host - keeping it real.研究自然宿主中的人畜共患病免疫——保持真实。
Nat Rev Immunol. 2013 Dec;13(12):851-61. doi: 10.1038/nri3551. Epub 2013 Oct 25.
2
Review: influenza virus in pigs.综述:猪流感病毒。
Mol Immunol. 2013 Oct;55(3-4):200-11. doi: 10.1016/j.molimm.2013.02.008. Epub 2013 Mar 21.
3
Porcine CD8αdim/-NKp46high NK cells are in a highly activated state.猪 CD8αdim/-NKp46high NK 细胞处于高度激活状态。
猪流感 A 病毒和猪繁殖与呼吸综合征病毒的同时感染增强了适应性免疫反应。
Front Immunol. 2023 May 23;14:1192604. doi: 10.3389/fimmu.2023.1192604. eCollection 2023.
4
Porcine Plasmacytoid Dendritic Cells Are Unique in Their Expression of a Functional NKp46 Receptor.猪浆细胞样树突状细胞在表达功能性 NKp46 受体方面具有独特性。
Front Immunol. 2022 Mar 11;13:822258. doi: 10.3389/fimmu.2022.822258. eCollection 2022.
5
The Natural Cytotoxicity Receptor NKp44 (NCR2, CD336) Is Expressed on the Majority of Porcine NK Cells Without Stimulation.天然细胞毒性受体 NKp44(NCR2,CD336)在未经刺激的大多数猪 NK 细胞上表达。
Front Immunol. 2022 Jan 28;13:767530. doi: 10.3389/fimmu.2022.767530. eCollection 2022.
6
Guidelines for the use of flow cytometry and cell sorting in immunological studies (second edition).流式细胞术和细胞分选在免疫学研究中的应用指南(第二版)。
Eur J Immunol. 2019 Oct;49(10):1457-1973. doi: 10.1002/eji.201970107.
7
The Role of Innate Leukocytes during Influenza Virus Infection.固有免疫细胞在流感病毒感染中的作用。
J Immunol Res. 2019 Sep 12;2019:8028725. doi: 10.1155/2019/8028725. eCollection 2019.
8
Experimental H1N1pdm09 infection in pigs mimics human seasonal influenza infections.猪感染实验性 H1N1pdm09 可模拟人类季节性流感感染。
PLoS One. 2019 Sep 20;14(9):e0222943. doi: 10.1371/journal.pone.0222943. eCollection 2019.
9
Cellular Innate Immunity against PRRSV and Swine Influenza Viruses.针对猪繁殖与呼吸综合征病毒和猪流感病毒的细胞先天性免疫
Vet Sci. 2019 Mar 11;6(1):26. doi: 10.3390/vetsci6010026.
10
Altered Natural Killer Cell Function in HIV-Exposed Uninfected Infants.暴露于HIV但未感染婴儿的自然杀伤细胞功能改变
Front Immunol. 2017 Apr 24;8:470. doi: 10.3389/fimmu.2017.00470. eCollection 2017.
Vet Res. 2013 Mar 1;44(1):13. doi: 10.1186/1297-9716-44-13.
4
Phenotypic maturation of porcine NK- and T-cell subsets.猪 NK 细胞和 T 细胞亚群的表型成熟。
Dev Comp Immunol. 2013 May;40(1):51-68. doi: 10.1016/j.dci.2013.01.003. Epub 2013 Jan 22.
5
The bone marrow functions as the central site of proliferation for long-lived NK cells.骨髓是长寿命 NK 细胞增殖的中心部位。
J Immunol. 2012 Sep 1;189(5):2333-7. doi: 10.4049/jimmunol.1200008. Epub 2012 Jul 20.
6
Global transmission of influenza viruses from humans to swine.流感病毒在全球范围内从人类传播到猪。
J Gen Virol. 2012 Oct;93(Pt 10):2195-2203. doi: 10.1099/vir.0.044974-0. Epub 2012 Jul 12.
7
A review on the clinical spectrum and natural history of human influenza.关于人类流感的临床谱和自然史的综述。
Int J Infect Dis. 2012 Oct;16(10):e714-23. doi: 10.1016/j.ijid.2012.05.1025. Epub 2012 Jul 10.
8
NKp46 expression discriminates porcine NK cells with different functional properties.NKp46 表达可区分具有不同功能特性的猪 NK 细胞。
Eur J Immunol. 2012 May;42(5):1261-71. doi: 10.1002/eji.201141989.
9
Severe pandemic H1N1 2009 infection is associated with transient NK and T deficiency and aberrant CD8 responses.严重的 2009 年甲型 H1N1 大流行感染与 NK 和 T 细胞一过性缺失以及异常的 CD8 反应有关。
PLoS One. 2012;7(2):e31535. doi: 10.1371/journal.pone.0031535. Epub 2012 Feb 20.
10
The pig: a model for human infectious diseases.猪:人类传染病的模型。
Trends Microbiol. 2012 Jan;20(1):50-7. doi: 10.1016/j.tim.2011.11.002. Epub 2011 Dec 5.