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白细胞介素-12缺乏在小鼠甲型流感病毒呼吸道感染后期短暂改善病毒清除。

IL-12 deficiency transiently improves viral clearance during the late phase of respiratory tract infection with influenza A virus in mice.

作者信息

van der Sluijs Koenraad F, van Elden Leontine J R, Xiao Yanling, Arens Ramon, Nijhuis Monique, Schuurman Rob, Florquin Sandrine, Jansen Henk M, Lutter René, van der Poll Tom

机构信息

Laboratory of Experimental Internal Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Antiviral Res. 2006 Jun;70(2):75-84. doi: 10.1016/j.antiviral.2006.01.007. Epub 2006 Feb 9.

DOI:10.1016/j.antiviral.2006.01.007
PMID:16490265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7126924/
Abstract

T helper 1-driven immune responses have been implicated in protective immunity against viral infections. Interleukin (IL)-12 is a heterodimeric proinflammatory cytokine formed by a p35 and a p40 subunit that can induce differentiation of naïve T cells towards a T helper 1-response. To determine the role of IL-12 in respiratory tract infection with influenza, p35 gene deficient (p35-/-) and normal wild type mice were intranasally infected with influenza A virus. IL-12 p35-/- mice displayed a transiently enhanced rather than an impaired viral clearance, as indicated by a 10-fold reduction in viral loads on day 8 after infection. Although interferon-gamma levels were significantly lower in the lungs of IL-12 p35-/- mice, their cellular immune responses were not altered, as reflected by similar T cell CD69 expression and influenza-specific T cell recruitment. Our data indicate that endogenous IL-12 impairs viral clearance during the late phase of influenza A virus infection in mice.

摘要

辅助性T细胞1驱动的免疫反应与针对病毒感染的保护性免疫有关。白细胞介素(IL)-12是一种由p35和p40亚基组成的异源二聚体促炎细胞因子,可诱导初始T细胞向辅助性T细胞1反应分化。为了确定IL-12在流感病毒呼吸道感染中的作用,将p35基因缺陷(p35-/-)小鼠和正常野生型小鼠经鼻感染甲型流感病毒。感染后第8天病毒载量降低了10倍,这表明IL-12 p35-/-小鼠的病毒清除呈短暂增强而非受损。尽管IL-12 p35-/-小鼠肺中的干扰素-γ水平显著降低,但它们的细胞免疫反应并未改变,这可通过相似的T细胞CD69表达和流感特异性T细胞募集反映出来。我们的数据表明,内源性IL-12在小鼠甲型流感病毒感染后期会损害病毒清除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/0c0d96450010/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/c0ef2c80cb61/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/16d374df94b7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/58fac6c7920f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/1fa3442001ba/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/1a954b2fa101/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/651f957d2539/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/7e28c828a026/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/0c0d96450010/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/c0ef2c80cb61/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/16d374df94b7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/58fac6c7920f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/1fa3442001ba/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/1a954b2fa101/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/651f957d2539/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/7e28c828a026/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e421/7126924/0c0d96450010/gr8.jpg

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本文引用的文献

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J Exp Med. 2005 Mar 21;201(6):937-47. doi: 10.1084/jem.20041901.
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Immunology. 2005 Jan;114(1):112-20. doi: 10.1111/j.1365-2567.2004.02000.x.
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Role of IgA versus IgG in the control of influenza viral infection in the murine respiratory tract.
鸡细胞因子 IL-12 整合入表达禽流感病毒神经氨酸酶 N1 的重组禽痘病毒对宿主细胞免疫应答的影响可忽略不计。
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Interferon induced protein 35 exacerbates H5N1 influenza disease through the expression of IL-12p40 homodimer.干扰素诱导蛋白 35 通过表达 IL-12p40 同源二聚体加重 H5N1 流感疾病。
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Interleukin-15 is critical in the pathogenesis of influenza a virus-induced acute lung injury.白细胞介素-15 在甲型流感病毒诱导的急性肺损伤发病机制中起关键作用。
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IgA与IgG在小鼠呼吸道流感病毒感染控制中的作用。
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