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Pattern recognition receptor MDA5 modulates CD8+ T cell-dependent clearance of West Nile virus from the central nervous system.模式识别受体 MDA5 调节 CD8+T 细胞依赖性清除西尼罗河病毒从中枢神经系统。
J Virol. 2013 Nov;87(21):11401-15. doi: 10.1128/JVI.01403-13. Epub 2013 Aug 21.
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A systems biology approach reveals that tissue tropism to West Nile virus is regulated by antiviral genes and innate immune cellular processes.系统生物学方法揭示,组织对西尼罗河病毒的嗜性受抗病毒基因和固有免疫细胞过程的调节。
PLoS Pathog. 2013 Feb;9(2):e1003168. doi: 10.1371/journal.ppat.1003168. Epub 2013 Feb 7.
3
CD22 is required for protection against West Nile virus Infection.CD22 对于抵抗西尼罗河病毒感染是必需的。
J Virol. 2013 Mar;87(6):3361-75. doi: 10.1128/JVI.02368-12. Epub 2013 Jan 9.
4
Trafficking and replication patterns reveal splenic macrophages as major targets of dengue virus in mice. trafficking 和 replication patterns 揭示了脾脏巨噬细胞是登革热病毒在小鼠中的主要靶标。
J Virol. 2012 Nov;86(22):12138-47. doi: 10.1128/JVI.00375-12. Epub 2012 Aug 29.
5
Intrinsic adjuvanting of a novel single-cycle flavivirus vaccine in the absence of type I interferon receptor signaling.新型单周期黄病毒疫苗在不存在 I 型干扰素受体信号的情况下的内在佐剂作用。
Vaccine. 2012 Feb 14;30(8):1465-75. doi: 10.1016/j.vaccine.2011.12.103. Epub 2012 Jan 5.
6
CD169+ macrophages at the crossroads of antigen presentation.CD169+ 巨噬细胞在抗原呈递的十字路口。
Trends Immunol. 2012 Feb;33(2):66-70. doi: 10.1016/j.it.2011.11.001. Epub 2011 Dec 21.
7
A temporal role of type I interferon signaling in CD8+ T cell maturation during acute West Nile virus infection.I 型干扰素信号在急性西尼罗河病毒感染期间 CD8+T 细胞成熟中的临时作用。
PLoS Pathog. 2011 Dec;7(12):e1002407. doi: 10.1371/journal.ppat.1002407. Epub 2011 Dec 1.
8
Interferon regulatory factor-1 (IRF-1) shapes both innate and CD8(+) T cell immune responses against West Nile virus infection.干扰素调节因子-1(IRF-1)塑造了针对西尼罗河病毒感染的先天和 CD8(+)T 细胞免疫反应。
PLoS Pathog. 2011 Sep;7(9):e1002230. doi: 10.1371/journal.ppat.1002230. Epub 2011 Sep 1.
9
Beta interferon controls West Nile virus infection and pathogenesis in mice.β干扰素控制西尼罗河病毒在小鼠中的感染和发病机制。
J Virol. 2011 Jul;85(14):7186-94. doi: 10.1128/JVI.00396-11. Epub 2011 May 4.
10
Immunogenicity of RepliVAX WN, a novel single-cycle West Nile virus vaccine.新型单周期西尼罗河病毒疫苗 RepliVAX WN 的免疫原性。
Vaccine. 2010 Dec 16;29(2):174-82. doi: 10.1016/j.vaccine.2010.10.069. Epub 2010 Nov 4.

包膜下窦巨噬细胞限制接种后西尼罗河病毒颗粒的扩散,但对西尼罗河病毒特异性 T 细胞反应的发展并非必不可少。

Subcapsular sinus macrophages limit dissemination of West Nile virus particles after inoculation but are not essential for the development of West Nile virus-specific T cell responses.

机构信息

Department of Pathology, University of Texas Medical Branch (UTMB), Galveston, TX 77555, USA.

Department of Microbiology and Immunology, UTMB, Galveston, TX, USA.

出版信息

Virology. 2014 Feb;450-451:278-89. doi: 10.1016/j.virol.2013.12.021. Epub 2014 Jan 10.

DOI:10.1016/j.virol.2013.12.021
PMID:24503091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3939857/
Abstract

Macrophages encounter flaviviruses early after injection by arthropod vectors. Using in vivo imaging of mice inoculated with firefly luciferase-expressing single-cycle flavivirus particles (FLUC-SCFV), we examined the initial dissemination of virus particles in the presence or absence of lymph node (LN)-resident macrophages. Higher luciferase activity, indicating higher SCFV gene expression, was detected in the footpad of macrophage-depleted mice after 24h post infection (hpi). Moreover, FLUC-SCFV particles disseminated to the spleen within 14 hpi in macrophage-depleted, but not control mice. Although macrophages presented SCFV to naïve T cells in vitro, depletion of subcapsular sinus (SCS) macrophages did not alter the magnitude or effector function of the WNV-specific CD8(+) T cell response. Together, these results indicate that SCS macrophages play a role in limiting the dissemination of SCFV early in infection but are not required for the generation of a polyfunctional WNV-specific CD8(+) T cell response in the draining LN.

摘要

在节肢动物载体注射后,巨噬细胞会很快遇到黄病毒。通过对感染萤火虫荧光素酶表达的单循环黄病毒颗粒(FLUC-SCFV)的小鼠进行体内成像,我们研究了在存在或不存在淋巴结(LN)驻留巨噬细胞的情况下,病毒颗粒的初始传播情况。在感染后 24 小时(hpi),巨噬细胞耗竭小鼠的足垫中检测到更高的荧光素酶活性,表明更高的 SCFV 基因表达。此外,在巨噬细胞耗竭的小鼠中,FLUC-SCFV 颗粒在 14 hpi 时传播到脾脏,而在对照小鼠中则没有。尽管巨噬细胞在体外将 SCFV 呈递给幼稚 T 细胞,但对被膜下窦(SCS)巨噬细胞的耗竭并未改变 WNV 特异性 CD8(+) T 细胞反应的幅度或效应功能。综上所述,这些结果表明 SCS 巨噬细胞在感染早期限制 SCFV 的传播中发挥作用,但在引流 LN 中产生多功能 WNV 特异性 CD8(+) T 细胞反应时不需要 SCS 巨噬细胞。