首页> 外文期刊>Frontiers in Immunology >Exploitation of Scavenger Receptor, Macrophage Receptor with Collagenous Structure, by Cryptococcus neoformans Promotes Alternative Activation of Pulmonary Lymph Node CD11b + Conventional Dendritic Cells and Non-Protective Th2 Bias
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Exploitation of Scavenger Receptor, Macrophage Receptor with Collagenous Structure, by Cryptococcus neoformans Promotes Alternative Activation of Pulmonary Lymph Node CD11b + Conventional Dendritic Cells and Non-Protective Th2 Bias

机译:清除剂的清除剂受体,巨噬细胞受体具有胶原结构,通过<斜斜体>斜氏链球菌Neoformans 促进肺淋巴结CD11b + 常规树突细胞和非保护性Th2偏置的替代活化

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Macrophage receptor with collagenous structure (MARCO) contributes to fungal containment during the early/innate phase of cryptococcal infection; however, its role in adaptive antifungal immunity remains unknown. Using a murine model of cryptococcosis, we compared host adaptive immune responses in wild-type and MARCO~(?/?)mice throughout an extended time course post-infection. Unlike in early infection, MARCO deficiency resulted in improved pulmonary fungal clearance and diminished cryptococcal dissemination during the efferent phase. Improved fungal control in the absence of MARCO expression was associated with enhanced hallmarks of protective Th1-immunity, including higher frequency of pulmonary TNF-α-producing T cells, increased cryptococcal-antigen-triggered IFN-γ and TNF-α production by splenocytes, and enhanced expression of M1 polarization genes by pulmonary macrophages. Concurrently, we found lower frequencies of IL-5- and IL-13-producing T cells in the lungs, impaired production of IL-4 and IL-10 by cryptococcal antigen-pulsed splenocytes, and diminished serum IgE, which were hallmarks of profoundly suppressed efferent Th2 responses in MARCO-deficient mice compared to WT mice. Mechanistically, we found that MARCO expression facilitated early accumulation and alternative activation of CD11b~(+)conventional DC (cDC) in the lung-associated lymph nodes (LALNs), which contributed to the progressive shift of the immune response from Th1 toward Th2 at the priming site (LALNs) and local infection site (lungs) during the efferent phase of cryptococcal infection. Taken together, our study shows that MARCO can be exploited by the fungal pathogen to promote accumulation and alternative activation of CD11b~(+)cDC in the LALN, which in turn alters Th1/Th2 balance to promote fungal persistence and dissemination.
机译:具有胶原结构(MARCO)的巨噬细胞受体有助于在密集的密集液感染期间的真菌遏制;然而,其在适应性抗真菌免疫中的作用仍然是未知的。利用鼠模型的隐色病变,我们在伴随时间课程后野生型和Marco〜(β/β)小鼠中的宿主自适应免疫应答。与早期感染不同,MARCO缺陷导致肺部肺部肺部清除和在迁移阶段期间的肺炎骨膜溶解减少。在没有Marco表达的情况下,改善的真菌控制与增强的保护性Th1-achity的标志有关,包括肺炎TNF-α产生的T细胞的较高频率,增加了脾细胞的肾上腺炎抗原触发的IFN-γ和TNF-α产生。肺巨噬细胞增强M1偏振基因的表达。同时,我们发现肺中IL-5和IL-13产生的T细胞较低的频率,通过隐性球菌抗原 - 脉冲脾细胞损害IL-4和IL-10,并降低血清IgE,这是深刻的标志与WT小鼠相比,抑制了Marco缺陷小鼠中的散发剂Th2反应。机械地,我们发现Marco表达促进了肺相关淋巴结(LALN)中CD11b〜(+)常规DC(CDC)的早期积累和替代活化,这有助于免疫应答从TH1朝向TH2在密集膜感染的迁移阶段期间引发位点(LALNS)和局部感染部位(肺)。我们的研究表明,Marco可以被真菌病原体利用,以促进LALN中CD11b〜(+)CDC的积累和替代活化,这反过来改变了TH1 / TH2平衡,以促进真菌持久性和传播。

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