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小鼠肺部对荚膜组织胞浆菌的初次免疫反应的演变

Evolution of the primary immune response to Histoplasma capsulatum in murine lung.

作者信息

Cain J A, Deepe G S

机构信息

Department of Medicine, University of Cincinnati College of Medicine, Ohio 45267-0560, USA.

出版信息

Infect Immun. 1998 Apr;66(4):1473-81. doi: 10.1128/IAI.66.4.1473-1481.1998.

Abstract

Histoplasma capsulatum induces a cell-mediated immune response in the lungs and lymphoid organs of mammals. In this study, we analyzed the progression of the cytokine and inflammatory reactions in the lungs of mice infected intranasally with H. capsulatum. We measured cytokine mRNA levels and determined the inflammatory cell populations during the active phase of infection (<3 weeks). Transcription of genes encoding interleukin-2 (IL-2), IL-4, and IL-12 and gamma interferon (IFN-gamma) was detectable as early as day 3 of infection, whereas a signal for IL-10 was never observed. Competitive PCR analysis demonstrated that enhanced expression of IL-12 mRNA was observed by day 3 and that expression of mRNA for IL-2 and IFN-gamma progressively increased from day 5 to day 10. All levels declined by day 14. Analysis of the inflammatory response revealed an initial elevation in myeloid cells (Mac-1+) and natural killer (NK) cells followed by a rise in T cells, predominantly CD4+ cells. Since IFN-gamma is a key factor in host defense, we performed cytoplasmic staining to determine the cell populations that produced this cytokine. The hierarchy of synthesis was CD4+ > CD8+ > NK cells. Thus, H. capsulatum provokes an orderly modulation of the inflammatory and cytokine responses in murine lungs.

摘要

荚膜组织胞浆菌可在哺乳动物的肺部和淋巴器官中引发细胞介导的免疫反应。在本研究中,我们分析了经鼻内感染荚膜组织胞浆菌的小鼠肺部细胞因子和炎症反应的进展情况。我们在感染的活跃期(<3周)测量了细胞因子mRNA水平,并确定了炎症细胞群体。早在感染第3天就能检测到编码白细胞介素-2(IL-2)、IL-4、IL-12和γ干扰素(IFN-γ)的基因转录,而从未观察到IL-10的信号。竞争性PCR分析表明,在第3天观察到IL-12 mRNA表达增强,并且IL-2和IFN-γ的mRNA表达从第5天到第10天逐渐增加。到第14天所有水平均下降。对炎症反应的分析显示,髓样细胞(Mac-1+)和自然杀伤(NK)细胞最初升高,随后T细胞增多,主要是CD4+细胞。由于IFN-γ是宿主防御中的关键因子,我们进行了细胞质染色以确定产生这种细胞因子的细胞群体。合成顺序为CD4+>CD8+>NK细胞。因此,荚膜组织胞浆菌可引发小鼠肺部炎症和细胞因子反应的有序调节。

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