首页> 外文期刊>Clinical and Experimental Immunology: An Official Journal of the British Society for Immunology >Attenuation of massive cytokine response to the staphylococcal enterotoxin B superantigen by the innate immunomodulatory protein lactoferrin.
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Attenuation of massive cytokine response to the staphylococcal enterotoxin B superantigen by the innate immunomodulatory protein lactoferrin.

机译:先天性免疫调节蛋白乳铁蛋白对葡萄球菌肠毒素B超抗原的大量细胞因子的反应减弱。

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摘要

Staphylococcal enterotoxin B (SEB) is a pyrogenic exotoxin and a potent superantigen which causes massive T cell activation and cytokine secretion, leading to profound immunosuppression and morbidity. The inhibition of SEB-induced responses is thus considered a goal in the management of certain types of staphylococcal infections. Lactoferrin (LF) is a multi-functional glycoprotein with both bacteriostatic and bactericidal activities. In addition, LF is known to have potent immunomodulatory properties. Given the anti-microbial and anti-inflammatory properties of this protein, we hypothesized that LF can modulate T cell responses to SEB. Here, we report that bovine LF (bLF) was indeed able to attenuate SEB-induced proliferation, interleukin-2 production and CD25 expression by human leucocyte antigen (HLA)-DR4 transgenic mouse T cells. This inhibition was not due to bLF's iron-binding capacity, and could be mimicked by the bLF-derived peptide lactoferricin. Cytokine secretion by an engineered SEB-responsive human Jurkat T cell line and by peripheral blood mononuclear cells from healthy donors was also inhibited by bLF. These findings reveal a previously unrecognized property of LF in modulation of SEB-triggered immune activation and suggest a therapeutic potential for this naturally occurring protein during toxic shock syndrome.
机译:葡萄球菌肠毒素B(SEB)是一种热原性外毒素,是一种强效超抗原,可引起大量T细胞活化和细胞因子分泌,从而导致严重的免疫抑制和发病。因此,抑制SEB诱导的反应被认为是某些类型葡萄球菌感染管理的目标。乳铁蛋白(LF)是一种多功能糖蛋白,具有抑菌和杀菌作用。另外,已知LF具有有效的免疫调节特性。鉴于该蛋白的抗微生物和抗炎特性,我们假设LF可以调节T细胞对SEB的反应。在这里,我们报告牛LF(bLF)确实能够通过人白细胞抗原(HLA)-DR4转基因小鼠T细胞减弱SEB诱导的增殖,白介素2的产生和CD25的表达。这种抑制不是由于bLF的铁结合能力引起的,而可以被bLF衍生的肽乳铁蛋白所模仿。 bLF还抑制了工程化SEB响应性人Jurkat T细胞系和健康供体的外周血单核细胞分泌的细胞因子。这些发现揭示了LF在调节SEB触发的免疫激活中的先前无法识别的特性,并暗示了这种天然存在的蛋白在中毒性休克综合症中的治疗潜力。

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