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慢性 Q 热患者外周血单个核细胞对柯克斯体的完整干扰素-γ反应。

Intact interferon-γ response against Coxiella burnetii by peripheral blood mononuclear cells in chronic Q fever.

机构信息

Department of Internal Medicine and Radboud Center for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.

URMITE, CNRS UMR 7278, IRD 198, INSERM 1095, Aix-Marseille University, Marseille, France.

出版信息

Clin Microbiol Infect. 2017 Mar;23(3):209.e9-209.e15. doi: 10.1016/j.cmi.2016.11.008. Epub 2016 Nov 20.

Abstract

OBJECTIVES

Q fever is caused by Coxiella burnetii, an intracellular bacterium that infects phagocytes. The aim of the present study was to investigate whether the C. burnetii-induced IFN-γ response is defective in chronic Q fever patients.

METHODS

IFN-γ was measured in supernatants of C. burnetii-stimulated peripheral blood mononuclear cells (PBMCs) of 17 chronic Q fever patients and 17 healthy individuals. To assess IFN-γ responses, expression profiles of IFN-γ-induced genes in C. burnetii-stimulated PBMCs were studied in six patients and four healthy individuals. Neopterin was measured in PBMC supernatants (of eight patients and four healthy individuals) and in sera (of 21 patients and 11 healthy individuals). In a genetic association study, polymorphisms in genes involved in the Th1-cytokine response were analysed in a cohort of 139 chronic Q fever patients and a cohort of 220 control individuals with previous exposition to C. burnetii.

RESULTS

IFN-γ production by C. burnetii-stimulated PBMCs from chronic Q fever patients was significantly higher than in healthy controls. Many IFN-γ response genes were strongly upregulated in PBMCs of patients. Neopterin levels were significantly higher in PBMC supernatants and sera of patients. The IL12B polymorphisms rs3212227 and rs2853694 were associated with chronic Q fever.

CONCLUSIONS

IFN-γ production, as well as the response to IFN-γ, is intact in chronic Q fever patients, and even higher than in healthy individuals. Polymorphisms in the IL-12p40 gene are associated with chronic Q fever. Thus, a deficiency in IFN-γ responses does not explain the failure to clear the infection. The genetic data suggest, however, that the IL-12/IFN-γ pathway does play a role.

摘要

目的

Q 热是由柯克斯体引起的,这是一种感染吞噬细胞的细胞内细菌。本研究旨在探讨慢性 Q 热患者的 C. burnetii 诱导 IFN-γ 反应是否存在缺陷。

方法

测量了 17 例慢性 Q 热患者和 17 名健康个体的外周血单个核细胞(PBMC)中 C. burnetii 刺激后的 IFN-γ。为了评估 IFN-γ 反应,研究了 6 例患者和 4 名健康个体中 C. burnetii 刺激后的 PBMC 中 IFN-γ 诱导基因的表达谱。在 8 例患者和 4 名健康个体的 PBMC 上清液中和 21 例患者和 11 名健康个体的血清中测量了新蝶呤。在一项遗传关联研究中,分析了 139 例慢性 Q 热患者和 220 例曾暴露于 C. burnetii 的对照个体中参与 Th1 细胞因子反应的基因的多态性。

结果

慢性 Q 热患者的 C. burnetii 刺激 PBMC 产生 IFN-γ的水平明显高于健康对照组。患者 PBMC 中许多 IFN-γ 反应基因被强烈上调。患者 PBMC 上清液和血清中的新蝶呤水平明显升高。IL12B 基因的 rs3212227 和 rs2853694 多态性与慢性 Q 热相关。

结论

慢性 Q 热患者的 IFN-γ 产生及其对 IFN-γ 的反应是完整的,甚至高于健康个体。IL-12p40 基因的多态性与慢性 Q 热相关。因此,IFN-γ 反应的缺陷不能解释感染无法清除的原因。遗传数据表明,IL-12/IFN-γ 途径确实发挥了作用。

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