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首页> 外文期刊>Clinical and Experimental Immunology: An Official Journal of the British Society for Immunology >Exposure to anthrax toxin alters human leucocyte expression of anthrax toxin receptor 1
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Exposure to anthrax toxin alters human leucocyte expression of anthrax toxin receptor 1

机译:接触炭疽毒素会改变人类白细胞炭疽毒素受体1的表达

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Anthrax is a toxin-mediated disease, the lethal effects of which are initiated by the binding of protective antigen (PA) with one of three reported cell surface toxin receptors (ANTXR). Receptor binding has been shown to influence host susceptibility to the toxins. Despite this crucial role for ANTXR in the outcome of disease, and the reported immunomodulatory consequence of the anthrax toxins during infection, little is known about ANTXR expression on human leucocytes. We characterized the expression levels of ANTXR1 (TEM8) on human leucocytes using flow cytometry. In order to assess the effect of prior toxin exposure on ANTXR1 expression levels, leucocytes from individuals with no known exposure, those exposed to toxin through vaccination and convalescent individuals were analysed. Donors could be defined as either 'low' or 'high' expressers based on the percentage of ANTXR1-positive monocytes detected. Previous exposure to toxins appears to modulate ANTXR1 expression, exposure through active infection being associated with lower receptor expression. A significant correlation between low receptor expression and high anthrax toxin-specific interferon (IFN)-γ responses was observed in previously infected individuals. We propose that there is an attenuation of ANTXR1 expression post-infection which may be a protective mechanism that has evolved to prevent reinfection.
机译:炭疽病是一种毒素介导的疾病,其致命作用是由保护性抗原(PA)与三种报告的细胞表面毒素受体(ANTXR)之一结合而引发的。受体结合已显示影响宿主对毒素的敏感性。尽管ANTXR在疾病的结果中起着至关重要的作用,而且据报道感染过程中炭疽毒素具有免疫调节作用,但关于ANTXR在人白细胞上的表达知之甚少。我们使用流式细胞术表征了ANTXR1(TEM8)在人白细胞上的表达水平。为了评估以前的毒素暴露对ANTXR1表达水平的影响,分析了来自未知暴露个体的白细胞,通过疫苗接种和恢复性个体暴露于毒素的白细胞。根据检测到的ANTXR1阳性单核细胞的百分比,可以将供体定义为“低”或“高”表达。以前接触毒素似乎可以调节ANTXR1的表达,通过主动感染的接触与较低的受体表达有关。在先前感染的个体中观察到低受体表达与高炭疽毒素特异性干扰素(IFN)-γ反应之间的显着相关性。我们建议感染后ANTXR1表达减弱,这可能是预防再感染的保护机制。

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