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本文引用的文献

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The life cycle stages of Pneumocystis murina have opposing effects on the immune response to this opportunistic, fungal pathogen.鼠肺孢子菌的生命周期阶段对针对这种机会性真菌病原体的免疫反应具有相反的影响。
Infect Immun. 2016 Nov;84(11):3195-3205. doi: 10.1128/IAI.00519-16. Epub 2016 Aug 29.
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PU.1 Suppresses Th2 Cytokine Expression via Silencing of GATA3 Transcription in Dendritic Cells.PU.1 通过沉默树突状细胞中的 GATA3 转录来抑制 Th2 细胞因子表达。
PLoS One. 2015 Sep 11;10(9):e0137699. doi: 10.1371/journal.pone.0137699. eCollection 2015.
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Evidence for Proinflammatory β-1,6 Glucans in the Pneumocystis carinii Cell Wall.卡氏肺孢子虫细胞壁中促炎β-1,6葡聚糖的证据。
Infect Immun. 2015 Jul;83(7):2816-26. doi: 10.1128/IAI.00196-15. Epub 2015 Apr 27.
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Selective and efficient generation of functional Batf3-dependent CD103+ dendritic cells from mouse bone marrow.从小鼠骨髓中选择性高效地生成功能性依赖Batf3的CD103⁺树突状细胞。
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Organization of the mouse and human DC network.小鼠和人类树突状细胞网络的组织。
Curr Opin Immunol. 2014 Feb;26:90-9. doi: 10.1016/j.coi.2013.11.002. Epub 2013 Dec 3.
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IRF4 transcription factor-dependent CD11b+ dendritic cells in human and mouse control mucosal IL-17 cytokine responses.IRF4 转录因子依赖性 CD11b+ 树突状细胞控制人和小鼠黏膜 IL-17 细胞因子反应。
Immunity. 2013 May 23;38(5):970-83. doi: 10.1016/j.immuni.2013.04.011.
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STAT4-dependent and -independent Th2 responses correlate with protective immunity against lung infection with Pneumocystis murina.STAT4 依赖性和非依赖性 Th2 反应与对抗肺孢子菌肺炎感染的保护性免疫相关。
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The dendritic cell lineage: ontogeny and function of dendritic cells and their subsets in the steady state and the inflamed setting.树突状细胞谱系:在稳态和炎症环境中树突状细胞及其亚群的发生和功能。
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9
Conventional and monocyte-derived CD11b(+) dendritic cells initiate and maintain T helper 2 cell-mediated immunity to house dust mite allergen.传统的和单核细胞衍生的 CD11b(+)树突状细胞启动和维持尘螨变应原介导的辅助性 T 细胞 2 型免疫。
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Characterization of a distinct host response profile to Pneumocystis murina asci during clearance of pneumocystis pneumonia.在清除卡氏肺孢子虫肺炎期间,对卡氏肺孢子虫囊包体的独特宿主反应谱进行了表征。
Infect Immun. 2013 Mar;81(3):984-95. doi: 10.1128/IAI.01181-12. Epub 2013 Jan 14.

机会性真菌病原体鼠肺孢子菌的营养生命周期阶段阻碍了树突状细胞刺激CD4 T细胞反应的能力。

The Trophic Life Cycle Stage of the Opportunistic Fungal Pathogen Pneumocystis murina Hinders the Ability of Dendritic Cells To Stimulate CD4 T Cell Responses.

作者信息

Evans Heather M, Simpson Andrew, Shen Shu, Stromberg Arnold J, Pickett Carol L, Garvy Beth A

机构信息

Department of Microbiology, Immunology, and Molecular Genetics, University of Kentucky, Lexington, Kentucky, USA.

Department of Statistics, University of Kentucky, Lexington, Kentucky, USA.

出版信息

Infect Immun. 2017 Sep 20;85(10). doi: 10.1128/IAI.00396-17. Print 2017 Oct.

DOI:10.1128/IAI.00396-17
PMID:28694293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5607401/
Abstract

The life cycle of the opportunistic fungal pathogen consists of a trophic stage and an ascus-like cystic stage. Infection with the cyst stage induces proinflammatory immune responses, while trophic forms suppress the cytokine response to multiple pathogen-associated molecular patterns (PAMPs), including β-glucan. A targeted gene expression assay was used to evaluate the dendritic cell response following stimulation with trophic forms alone, with a normal mixture of trophic forms and cysts, or with β-glucan. We demonstrate that stimulation with trophic forms downregulated the expression of multiple genes normally associated with the response to infection, including genes encoding transcription factors. Trophic forms also suppressed the expression of genes related to antigen processing and presentation, including the gene encoding the major histocompatibility complex (MHC) class II transactivator, CIITA. Stimulation of dendritic cells with trophic forms, but not a mixture of trophic forms and cysts, reduced the expression of MHC class II and the costimulatory molecule CD40 on the surface of the cells. These defects in the expression of MHC class II and costimulatory molecules corresponded with a reduced capacity for trophic form-loaded dendritic cells to stimulate CD4 T cell proliferation and polarization. These data are consistent with the delayed innate and adaptive responses previously observed in immunocompetent mice inoculated with trophic forms compared to responses in mice inoculated with a mixture of trophic forms and cysts. We propose that trophic forms broadly inhibit the ability of dendritic cells to fulfill their role as antigen-presenting cells.

摘要

机会性真菌病原体的生命周期包括营养阶段和类子囊囊状阶段。囊状阶段的感染会诱导促炎性免疫反应,而营养型则会抑制对多种病原体相关分子模式(PAMP)(包括β-葡聚糖)的细胞因子反应。使用靶向基因表达分析来评估单独用营养型、营养型和囊状的正常混合物或β-葡聚糖刺激后树突状细胞的反应。我们证明,用营养型刺激会下调通常与感染反应相关的多个基因的表达,包括编码转录因子的基因。营养型还抑制了与抗原加工和呈递相关的基因的表达,包括编码主要组织相容性复合体(MHC)II类反式激活因子CIITA的基因。用营养型而非营养型和囊状的混合物刺激树突状细胞会降低细胞表面MHC II类和共刺激分子CD40的表达。MHC II类和共刺激分子表达的这些缺陷与负载营养型的树突状细胞刺激CD4 T细胞增殖和极化的能力降低相对应。这些数据与先前在接种营养型的免疫活性小鼠中观察到的先天性和适应性反应延迟一致,而与接种营养型和囊状混合物的小鼠的反应相比。我们提出,营养型广泛抑制树突状细胞作为抗原呈递细胞发挥作用的能力。