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接触炭疽毒素会改变人类白细胞中炭疽毒素受体 1 的表达。

Exposure to anthrax toxin alters human leucocyte expression of anthrax toxin receptor 1.

机构信息

Section of Infectious Diseases and Immunity, Department of Medicine Imperial College, Hammersmith Hospital, London.

出版信息

Clin Exp Immunol. 2013 Jul;173(1):84-91. doi: 10.1111/cei.12090.

Abstract

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.

摘要

炭疽是一种毒素介导的疾病,其致死效应是由保护性抗原 (PA) 与三种报道的细胞表面毒素受体 (ANTXR) 之一结合引发的。受体结合已被证明会影响宿主对毒素的易感性。尽管 ANTXR 在疾病结局中起着至关重要的作用,并且报道了炭疽毒素在感染期间的免疫调节作用,但人们对人类白细胞上的 ANTXR 表达知之甚少。我们使用流式细胞术对人类白细胞上的 ANTXR1(TEM8)表达水平进行了表征。为了评估先前毒素暴露对 ANTXR1 表达水平的影响,分析了无已知暴露、通过疫苗接种和恢复期个体暴露于毒素的个体的白细胞。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“低表达者”或“高表达者”。先前暴露于毒素似乎会调节 ANTXR1 的表达,通过主动感染暴露与受体表达降低有关。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 反应之间存在显著相关性。我们提出,感染后 ANTXR1 的表达会减弱,这可能是一种已进化的保护机制,旨在防止再次感染。

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本文引用的文献

1
Human genetic variation altering anthrax toxin sensitivity.
Proc Natl Acad Sci U S A. 2012 Feb 21;109(8):2972-7. doi: 10.1073/pnas.1121006109. Epub 2012 Feb 6.
3
A review of cutaneous anthrax and its outcome.
J Infect Public Health. 2010;3(3):98-105. doi: 10.1016/j.jiph.2010.07.004. Epub 2010 Aug 24.
4
Heterodimeric integrin complexes containing beta1-integrin promote internalization and lethality of anthrax toxin.
Proc Natl Acad Sci U S A. 2010 Aug 31;107(35):15583-8. doi: 10.1073/pnas.1010145107. Epub 2010 Aug 16.
6
An epitope of Bacillus anthracis protective antigen that is cryptic in rabbits may be immunodominant in humans.
Infect Immun. 2010 May;78(5):2353; author reply 2353-4. doi: 10.1128/IAI.00072-10.
7
Natural exposure to cutaneous anthrax gives long-lasting T cell immunity encompassing infection-specific epitopes.
J Immunol. 2010 Apr 1;184(7):3814-21. doi: 10.4049/jimmunol.0901581. Epub 2010 Mar 5.
8
Cutting edge: resistance to Bacillus anthracis infection mediated by a lethal toxin sensitive allele of Nalp1b/Nlrp1b.
J Immunol. 2010 Jan 1;184(1):17-20. doi: 10.4049/jimmunol.0903114. Epub 2009 Nov 30.
9
Bacillus anthracis lethal toxin disrupts TCR signaling in CD1d-restricted NKT cells leading to functional anergy.
PLoS Pathog. 2009 Sep;5(9):e1000588. doi: 10.1371/journal.ppat.1000588. Epub 2009 Sep 25.

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