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潜伏和活动性结核感染期间 IFN-γ、IL-17 和 IL-22 表达的 CD4 T 细胞、IL-22 表达的粒细胞和促炎细胞因子的比较。

Comparison of interferon-γ-, interleukin (IL)-17- and IL-22-expressing CD4 T cells, IL-22-expressing granulocytes and proinflammatory cytokines during latent and active tuberculosis infection.

机构信息

Ottawa Hospital Research Institute, Ottawa, ON, Canada.

出版信息

Clin Exp Immunol. 2012 Feb;167(2):317-29. doi: 10.1111/j.1365-2249.2011.04520.x.

Abstract

In this study, we investigated the role and expression of T helper type 17 (Th17) cells and Th17 cytokines in human tuberculosis. We show that the basal proportion of interferon (IFN)-γ-, interleukin (IL)-17- and IL-22-expressing CD4(+) T cells and IL-22-expressing granulocytes in peripheral blood were significantly lower in latently infected healthy individuals and active tuberculosis patients compared to healthy controls. In contrast, CD4(+) T cells expressing IL-17, IL-22 and IFN-γ were increased significantly following mycobacterial antigens stimulation in both latent and actively infected patients. Interestingly, proinflammatory IFN-γ and tumour necrosis factor (TNF)-α were increased following antigen stimulation in latent infection. Similarly, IL-1β, IL-4, IL-8, IL-22 and TNF-α were increased in the serum of latently infected individuals, whereas IL-6 and TNF-α were increased significantly in actively infected patients. Overall, we observed differential induction of IL-17-, IL-22- and IFN-γ-expressing CD4(+) T cells, IL-22-expressing granulocytes and proinflammatory cytokines in circulation and following antigenic stimulation in latent and active tuberculosis.

摘要

在这项研究中,我们研究了辅助性 T 细胞 17(Th17)细胞和 Th17 细胞因子在人类结核病中的作用和表达。我们发现,潜伏感染的健康个体和活动性结核病患者外周血中干扰素(IFN)-γ、白细胞介素(IL)-17 和 IL-22 表达的 CD4+T 细胞以及 IL-22 表达的粒细胞的基础比例明显低于健康对照者。相比之下,潜伏和活动性感染患者经分枝杆菌抗原刺激后,IL-17、IL-22 和 IFN-γ 表达的 CD4+T 细胞显著增加。有趣的是,潜伏感染后抗原刺激会导致促炎 IFN-γ 和肿瘤坏死因子(TNF)-α增加。同样,潜伏感染个体的血清中 IL-1β、IL-4、IL-8、IL-22 和 TNF-α增加,而活动性感染患者的 IL-6 和 TNF-α显著增加。总的来说,我们观察到潜伏和活动性结核病中,循环中以及抗原刺激后,IL-17、IL-22 和 IFN-γ 表达的 CD4+T 细胞、IL-22 表达的粒细胞和促炎细胞因子的诱导存在差异。

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本文引用的文献

1
Expression of the T helper 17-associated cytokines IL-17A and IL-17F in asthma and COPD.
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3
Suppression of IFNgamma+mycobacterial lipoarabinomannan-induced NO by IL-4 is due to decreased IRF-1 expression.
Tuberculosis (Edinb). 2009 Jul;89(4):294-303. doi: 10.1016/j.tube.2009.03.004. Epub 2009 Jun 24.
4
Regulation of interleukin-12/interleukin-23 production and the T-helper 17 response in humans.
Immunol Rev. 2008 Dec;226:112-31. doi: 10.1111/j.1600-065X.2008.00700.x.
5
Th17 cytokines and their emerging roles in inflammation and autoimmunity.
Immunol Rev. 2008 Dec;226:87-102. doi: 10.1111/j.1600-065X.2008.00712.x.
6
IL-17 and Th17 Cells.
Annu Rev Immunol. 2009;27:485-517. doi: 10.1146/annurev.immunol.021908.132710.
7
Interleukin-17 in host defence against bacterial, mycobacterial and fungal pathogens.
Immunology. 2009 Feb;126(2):177-85. doi: 10.1111/j.1365-2567.2008.03017.x.
8
Induction, function and regulation of IL-17-producing T cells.
Eur J Immunol. 2008 Oct;38(10):2636-49. doi: 10.1002/eji.200838535.
9
IL-23 promotes maintenance but not commitment to the Th17 lineage.
J Immunol. 2008 Nov 1;181(9):5948-55. doi: 10.4049/jimmunol.181.9.5948.

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