首页> 美国卫生研究院文献>Journal of Parasitology Research >Changes in T-Cell and Monocyte Phenotypes In Vitro by Schistosoma mansoni Antigens in Cutaneous Leishmaniasis Patients
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Changes in T-Cell and Monocyte Phenotypes In Vitro by Schistosoma mansoni Antigens in Cutaneous Leishmaniasis Patients

机译:曼氏血吸虫抗原在皮肤利什曼病患者体内T细胞和单核细胞表型的变化

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摘要

High levels of proinflammatory cytokines such as IFN-γ and TNF are associated with tissue lesions in cutaneous leishmaniasis (CL). We previously demonstrated that Schistosoma mansoni antigens downmodulate the in vitro cytokine response in CL. In the current study we evaluated whether S. mansoni antigens alter monocyte and T-lymphocyte phenotypes in leishmaniasis. Peripheral blood mononuclear cells of CL patients were cultured with L. braziliensis antigen in the presence or absence of the S. mansoni antigens rSm29, rSmTSP-2- and PIII. Cells were stained with fluorochrome conjugated antibodies and analyzed by flow cytometry. The addition of rSm29 to the cultures decreased the expression of HLA-DR in nonclassical (CD14+CD16++) monocytes, while the addition of PIII diminished the expression of this molecule in classical (CD14++CD16) and intermediate (CD14++CD16+) monocytes. The addition of PIII and rSmTSP-2 resulted in downmodulation of CD80 expression in nonclassical and CD86 expression in intermediate monocytes, respectively. These two antigens increased the expression of CTLA-4 in CD4+ T cells and they also expanded the frequency of CD4+CD25highFoxp3+ T cells. Taken together, we show that S. mansoni antigens, mainly rSmTSP-2 and PIII, are able to decrease the activation status of monocytes and also to upregulate the expression of modulatory molecules in T lymphocytes.
机译:高水平的促炎细胞因子(如IFN-γ和TNF)与皮肤利什曼病(CL)中的组织损伤有关。我们先前证明曼氏血吸虫抗原下调CL中的体外细胞因子反应。在本研究中,我们评估了曼氏链球菌抗原是否改变了利什曼病中的单核细胞和T淋巴细胞表型。在存在或不存在曼氏沙门氏菌抗原rSm29,rSmTSP-2-和PIII的情况下,用巴西乳杆菌抗原培养CL患者的外周血单核细胞。细胞用荧光染料偶联的抗体染色并通过流式细胞仪分析。向培养物中添加rSm29会降低非经典(CD14 + CD16 ++ )单核细胞中HLA-DR的表达,而PIII的添加会减少该分子的表达在经典(CD14 ++ CD16 -)和中间(CD14 ++ CD16 + )单核细胞中。 PIII和rSmTSP-2的添加分别导致非经典CD80表达下调和中间单核细胞CD86表达下调。这两种抗原增加了CD4 + T细胞中CTLA-4的表达,也增加了CD4 + CD25 high Foxp3 + T细胞。两者合计,我们表明曼氏链球菌抗原,主要是rSmTSP-2和PIII,能够降低单核细胞的激活状态,并且还可以上调T淋巴细胞中调节分子的表达。

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