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对痘苗病毒的初次和记忆 CD4 T 细胞应答中,CD80/86-CD28 共刺激的差异需求。

Differential requirements for CD80/86-CD28 costimulation in primary and memory CD4 T cell responses to vaccinia virus.

机构信息

Department of Microbiology and Immunology, Dartmouth Medical School, Lebanon, NH 03756, United States.

出版信息

Cell Immunol. 2011;266(2):130-4. doi: 10.1016/j.cellimm.2010.09.008. Epub 2010 Oct 30.

DOI:10.1016/j.cellimm.2010.09.008
PMID:21040905
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3053005/
Abstract

Vaccinia virus infection can confer immunity to smallpox by inducing potent T cell and antibody responses. While the CD8 T cell response to vaccinia virus has been well characterized, less is known about factors required for priming and memory for the CD4 T cells. Focusing on two recently described epitopes, we show that after intranasal infection, both I1L and L4R epitopes are co-dominant during the acute response, but the I1L epitope dominates during memory. CD4 T cell priming was intact in the absence of CD80/86, however secondary responses were reduced. This contrasts with our previous data showing CD80/86-CD28 interaction is required for optimal primary and memory CD8 T cell responses. The absence of CD80/86 also changed the immunodominance hierarchy during memory, with the I1L and L4R responses becoming co-dominant in knockout mice. These data highlight different costimulatory requirements for primary CD4 and CD8 T cell responses to vaccinia virus.

摘要

牛痘病毒感染可通过诱导有效的 T 细胞和抗体应答来提供对天花的免疫力。虽然已很好地描述了针对牛痘病毒的 CD8 T 细胞应答,但对于启动和记忆 CD4 T 细胞所需的因素知之甚少。我们专注于最近描述的两个表位,结果表明,在鼻内感染后,I1L 和 L4R 表位在急性反应期间都是共显性的,但在记忆中 I1L 表位占主导地位。尽管缺乏 CD80/86,但 CD4 T 细胞的初始阶段仍然完整,但是二次应答减少了。这与我们之前的数据形成对比,该数据表明 CD80/86-CD28 相互作用是最佳原发性和记忆性 CD8 T 细胞应答所必需的。缺乏 CD80/86 也改变了记忆期间的免疫优势等级,I1L 和 L4R 应答在敲除小鼠中变得共显性。这些数据突出了针对牛痘病毒的原发性 CD4 和 CD8 T 细胞应答的不同共刺激需求。

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本文引用的文献

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J Virol. 2009 Sep;83(17):8905-15. doi: 10.1128/JVI.00027-09. Epub 2009 Jun 24.
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Memory T cells need CD28 costimulation to remember.记忆性T细胞需要CD28共刺激来进行记忆。
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Preferential use of B7.2 and not B7.1 in priming of vaccinia virus-specific CD8 T cells.在痘苗病毒特异性CD8 T细胞启动过程中优先使用B7.2而非B7.1。
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Induction of death receptor CD95 and co-stimulatory molecules CD80 and CD86 by meningococcal capsular polysaccharide-loaded vaccine nanoparticles.脑膜炎球菌荚膜多糖负载的疫苗纳米颗粒对死亡受体CD95以及共刺激分子CD80和CD86的诱导作用。
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B7-1/B7-2 blockade overrides the activation of protective CD8 T cells stimulated in the absence of Foxp3+ regulatory T cells.B7-1/B7-2 阻断可克服在缺乏 Foxp3+调节性 T 细胞刺激下所产生的保护性 CD8 T 细胞的激活。
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A proteomic view at T cell costimulation.T 细胞共刺激的蛋白质组学观点。
PLoS One. 2012;7(4):e32994. doi: 10.1371/journal.pone.0032994. Epub 2012 Apr 23.
7
Multiple layers of CD80/86-dependent costimulatory activity regulate primary, memory, and secondary lymphocytic choriomeningitis virus-specific T cell immunity.多层 CD80/86 依赖性共刺激活性调节原发性、记忆性和继发性淋巴细胞性脉络丛脑膜炎病毒特异性 T 细胞免疫。
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Selective CD4+ T cell help for antibody responses to a large viral pathogen: deterministic linkage of specificities.针对大型病毒病原体抗体反应的选择性CD4 + T细胞辅助:特异性的确定性联系
Immunity. 2008 Jun;28(6):847-58. doi: 10.1016/j.immuni.2008.04.018.
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Vaccinia virus-specific CD4+ T cell responses target a set of antigens largely distinct from those targeted by CD8+ T cell responses.痘苗病毒特异性CD4+ T细胞应答所针对的一组抗原,在很大程度上不同于CD8+ T细胞应答所针对的抗原。
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Direct CD28 costimulation is required for CD8+ T cell-mediated resistance to an acute viral disease in a natural host.在天然宿主中,CD8⁺ T细胞介导的对急性病毒病的抵抗力需要CD28共刺激。
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Control of memory CD4 T cell recall by the CD28/B7 costimulatory pathway.通过CD28/B7共刺激途径对记忆性CD4 T细胞应答的调控。
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CD80 and CD86 control antiviral CD8+ T-cell function and immune surveillance of murine gammaherpesvirus 68.CD80和CD86调控抗小鼠γ疱疹病毒68的CD8⁺T细胞功能及免疫监视。
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