Evans Heather M, Simpson Andrew, Shen Shu, Stromberg Arnold J, Pickett Carol L, Garvy Beth A
Department of Microbiology, Immunology, and Molecular Genetics, University of Kentucky, Lexington, Kentucky, USA.
Department of Statistics, University of Kentucky, Lexington, Kentucky, USA.
Infect Immun. 2017 Sep 20;85(10). doi: 10.1128/IAI.00396-17. Print 2017 Oct.
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.
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。