首页> 外文期刊>Immunopharmacology and immunotoxicology >Tigecycline attenuates staphylococcal superantigen-induced T-cell proliferation and production of cytokines and chemokines.
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Tigecycline attenuates staphylococcal superantigen-induced T-cell proliferation and production of cytokines and chemokines.

机译:Tigecycline减弱葡萄球菌超抗原诱导的T细胞增殖以及细胞因子和趋化因子的产生。

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摘要

The purpose of this study is to examine the in vitro modulatory effect of tigecycline on staphylococcal superantigen-induced T-cell activation and cytokines and chemokines production by human peripheral blood mononuclear cells (PBMC). Isolated human PBMC from ten healthy volunteers were stimulated by staphylococcal enterotoxin B (SEB) and Staphylococcal toxic shock syndrome toxin-1 (TSST-1) superantigens with varying concentrations of tigecycline. Cytokines IL-1 beta, IL-6, TNF-alpha, and chemokines MIP-1 alpha and MIP-1 beta concentrations were measured along with T cell proliferation. Results demonstrated that tigecycline alters cytokine production and reduces T-cell proliferation in vitro suggesting an immunomodulatory activity independent of its antimicrobial effect.
机译:这项研究的目的是检查替加环素对人外周血单核细胞(PBMC)对葡萄球菌超抗原诱导的T细胞活化以及细胞因子和趋化因子产生的体外调节作用。从葡萄球菌肠毒素B(SEB)和葡萄球菌中毒性休克综合征毒素1(TSST-1)超抗原和不同浓度的替加环素刺激下,从十名健康志愿者中分离出人PBMC。测量了细胞因子IL-1β,IL-6,TNF-α和趋化因子MIP-1α和MIP-1β的浓度以及T细胞的增殖。结果表明,替加环素在体外可以改变细胞因子的产生并减少T细胞的增殖,提示其免疫调节活性与其抗微生物作用无关。

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