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免疫调节细胞因子与红鹿感染分枝杆菌副结核亚种后免受免疫病理损伤有关。

Immunoregulatory cytokines are associated with protection from immunopathology following Mycobacterium avium subspecies paratuberculosis infection in red deer.

机构信息

Department of Microbiology and Immunology, University of Otago, 720 Cumberland Street, Dunedin 9054, New Zealand.

出版信息

Infect Immun. 2011 May;79(5):2089-97. doi: 10.1128/IAI.00779-10. Epub 2011 Feb 14.

Abstract

Although the causative agent of Johne's disease, Mycobacterium avium subsp. paratuberculosis, is well known, the etiology of disease and the immune responses generated in response to infection are still poorly understood. Knowledge of definitive markers of protective immunity, infection, and the establishment of chronic granulomatous Johne's disease is necessary to advance vaccine and diagnostic development. We sought to profile the immune responses occurring within jejunal lymph nodes of experimentally challenged red deer (Cervus elaphus). Quantitative PCR was utilized to measure a range of cytokines, signaling molecules, and transcription factors involved in Th1, Th2, Treg, and Th17 immune responses. Significant differences in gene expression were observed between control, minimally diseased, and severely diseased animals, with severely diseased animals showing elevated proinflammatory transcripts and reduced anti-inflammatory transcripts. We identified a proinflammatory cytokine milieu of gamma interferon, interleukin-1α (IL-1α), and IL-17, which may contribute to the immunopathology observed during clinical Johne's disease and suggest that Th2 and Treg immune responses may play an important role in controlling the development of immunopathology in infected animals.

摘要

尽管约翰氏病的病原体——分枝杆菌副结核亚种(Mycobacterium avium subsp. paratuberculosis)已广为人知,但该病的病因以及感染后产生的免疫反应仍知之甚少。了解保护性免疫、感染和慢性肉芽肿性约翰氏病的确切标志物对于推进疫苗和诊断的发展是必要的。我们试图描绘实验性感染的红鹿(Cervus elaphus)空肠淋巴结中发生的免疫反应。我们利用定量 PCR 来测量一系列细胞因子、信号分子和转录因子,这些分子参与 Th1、Th2、Treg 和 Th17 免疫反应。在对照组、轻度患病组和严重患病组之间观察到基因表达存在显著差异,严重患病组表现出促炎转录本升高和抗炎转录本降低。我们鉴定出了一个促炎细胞因子环境,其中包括γ干扰素、白细胞介素-1α(IL-1α)和 IL-17,这可能有助于解释临床约翰氏病中观察到的免疫病理学,并表明 Th2 和 Treg 免疫反应可能在控制感染动物免疫病理学发展方面发挥重要作用。

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