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首页> 外文期刊>Inflammation >Development of Asthmatic Response upon Bronchial Allergen Challenge Is Associated with Dynamic Changes of Interleukin-10-Producing and Interleukin-10-Responding CD4+ T Cells
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Development of Asthmatic Response upon Bronchial Allergen Challenge Is Associated with Dynamic Changes of Interleukin-10-Producing and Interleukin-10-Responding CD4+ T Cells

机译:支气管过敏原激发后哮喘反应的发展与白细胞介素10产生和白细胞介素10响应的CD4 + T细胞的动态变化有关

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The role of adaptive immune system in regulation of asthmatic responses remains elusive. Here, we performed a comprehensive time-course analysis of mutual relationships between development of asthmatic response following allergen challenge and changes in several CD4+ T cell subsets which we characterized as either releasing interleukin-10 (CD4+CD25-CD127- and CD4+CD25+CD127+ T cells) or responding to IL-10 (CD4+ T cell subsets expressing CD210). Patients that developed asthmatic reaction were described as responders (R) whereas the others were named non-responders (NR). In R, in contrast to NR, at 6 h, we demonstrated significant expansion of CD4+CD25-CD127- T cells which was followed by drop to baseline values at 24 h. In contrast, in R, we observed decrease in numbers of CD4+CD25+CD127+ and CD4+CD25-CD127+ T cells at 24 h. Interestingly, at baseline, despite comparable IL-10 levels, R presented with lower levels of all CD4+ T cell subsets expressing CD210. In R, the numbers of CD4+CD210+ T cell subsets were further decreased following bronchial challenge which was paralleled by decrease in IL-10 serum levels. Altogether, our data suggest that dynamic interactions between IL-10-producing and IL-10-responding CD4+ T cells could contribute to pathogenesis of asthmatic responses in atopic individuals.
机译:适应性免疫系统在调节哮喘反应中的作用仍然难以捉摸。在这里,我们对变应原攻击后哮喘反应的发展与几个CD4 + T细胞亚群的变化之间的相互关系进行了全面的时程分析,我们将其表征为释放白介素10(CD4 + CD25-CD127-和CD4 + CD25 + CD127 + T细胞)或对IL-10有反应(表达CD210的CD4 + T细胞亚群)。发生哮喘反应的患者称为反应者(R),其他患者则称为无反应者(NR)。在R中,与NR相反,在6小时时,我们证明CD4 + CD25-CD127-T细胞显着扩增,随后在24小时时降至基线值。相反,在R中,我们观察到24小时CD4 + CD25 + CD127 +和CD4 + CD25-CD127 + T细胞数量减少。有趣的是,在基线时,尽管IL-10水平相当,但R表示所有表达CD210的CD4 + T细胞亚群的水平都较低。在R中,支气管激发后CD4 + CD210 + T细胞亚群的数量进一步减少,这与IL-10血清水平的降低相平行。总而言之,我们的数据表明产生IL-10的人与响应IL-10的CD4 + T细胞之间的动态相互作用可能有助于特应性个体发生哮喘反应。

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