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糖皮质激素在感染和炎症的小鼠模型中对特定细胞的免疫调节作用。

Cell-Specific Immune Regulation by Glucocorticoids in Murine Models of Infection and Inflammation.

机构信息

Department of Immunology, Institute for Biomedical Aging Research, University of Innsbruck, 6020 Innsbruck, Austria.

Institute for Developmental Immunology, Biocenter, Medical University of Innsbruck, 6020 Innsbruck, Austria.

出版信息

Cells. 2022 Jul 6;11(14):2126. doi: 10.3390/cells11142126.

Abstract

Glucocorticoids (GC) are highly potent negative regulators of immune and inflammatory responses. Effects of GC are primarily mediated by the glucocorticoid receptor (GR) which is expressed by all cell types of the immune system. It is, therefore, difficult to elucidate how endogenous GC mediate their effects on immune responses that involve multiple cellular interactions between various immune cell subsets. This review focuses on endogenous GC targeting specific cells of the immune system in various animal models of infection and inflammation. Without the timed release of these hormones, animals infected with various microbes or challenged in inflammatory disease models succumb as a consequence of overshooting immune and inflammatory responses. A clearer picture is emerging that endogenous GC thereby act in a cell-specific and disease model-dependent manner, justifying the need to develop techniques that target GC to individual immune cell types for improved clinical application.

摘要

糖皮质激素(GC)是免疫和炎症反应的强效负调节剂。GC 的作用主要通过糖皮质激素受体(GR)介导,GR 表达于免疫系统的所有细胞类型。因此,很难阐明内源性 GC 如何调节其对涉及各种免疫细胞亚群之间多种细胞相互作用的免疫反应的影响。本综述重点介绍了各种感染和炎症动物模型中内源性 GC 靶向免疫系统特定细胞的情况。如果没有这些激素的定时释放,感染各种微生物或在炎症性疾病模型中受到挑战的动物将因免疫和炎症反应过度而死亡。越来越清楚的是,内源性 GC 因此以细胞特异性和疾病模型依赖性的方式发挥作用,这证明需要开发针对特定免疫细胞类型的 GC 的技术,以实现更好的临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1dc/9324070/ebebfba5a620/cells-11-02126-g001.jpg

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