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糖皮质激素与炎症再探讨:最新进展。美国国立卫生研究院临床人员会议。

Glucocorticoids and inflammation revisited: the state of the art. NIH clinical staff conference.

作者信息

Franchimont Denis, Kino Tomoshige, Galon Jerome, Meduri Gianfranco Umberto, Chrousos George

机构信息

Pediatric and Reproductive Endocrinology Branch, NICHD, NIH, Bethesda, MD 20892-1583, USA.

出版信息

Neuroimmunomodulation. 2002;10(5):247-60. doi: 10.1159/000069969.

Abstract

Glucocorticoids have been used in the treatment of inflammatory and autoimmune diseases and to prevent graft rejection for over 50 years. These hormones exert their effects through cytoplasmic, heat shock protein-bound glucocorticoid receptors that translocate into the nucleus, where they regulate the transcriptional activity of responsive genes by binding to specific promoter DNA sequences (transactivation) or by interacting with transcription factors (transrepression). By interacting with different signaling pathways, newly characterized nuclear receptor coregulators enhance or diminish the actions of glucocorticoids, thus explaining the gene-, cell-, tissue- and context-dependent actions of glucocorticoids. Glucocorticoids modulate genes involved in the priming of the innate immune response, while their actions on the adaptive immune response are to suppress cellular [T helper (Th)1-directed] immunity and promote humoral (Th2-directed) immunity and tolerance. The past decade has produced new insights into the mechanisms of glucocorticoid sensitivity and resistance of inflammatory, autoimmune and allergic diseases. Both the quality and severity of the inflammatory stimulus, as well as the genetics and constitution of the patient, play key roles in the glucocorticoid sensitivity, dependency and resistance of these diseases. Although glucocorticoids increase susceptibility to opportunistic infections, they are also highly beneficial in the presence of serious systemic inflammation, such as that observed in septic shock and acute respiratory distress syndrome, when administered in a sustained fashion throughout the course of the disease. Glucocorticoids produce their cardiovascular, metabolic and antigrowth side effects through molecular mechanisms distinct from those involved in immunomodulation. Fortunately, the first generation of tissue- and immune- versus cardiovascular/metabolic effect-selective glucocorticoids is available for study and further improvement. 'Designer' glucocorticoids promise to be a great new advance in the therapy of inflammatory diseases.

摘要

糖皮质激素已用于治疗炎症性和自身免疫性疾病以及预防移植物排斥反应达50多年。这些激素通过与细胞质中热休克蛋白结合的糖皮质激素受体发挥作用,该受体易位进入细胞核,在细胞核中它们通过与特定启动子DNA序列结合(反式激活)或与转录因子相互作用(反式抑制)来调节反应性基因的转录活性。通过与不同的信号通路相互作用,新发现的核受体共调节因子增强或减弱糖皮质激素的作用,从而解释了糖皮质激素的基因、细胞、组织和环境依赖性作用。糖皮质激素调节参与先天免疫反应启动的基因,而它们对适应性免疫反应的作用是抑制细胞(T辅助细胞(Th)1介导的)免疫,促进体液(Th2介导的)免疫和耐受性。过去十年对炎症性、自身免疫性和过敏性疾病中糖皮质激素敏感性和耐药性的机制有了新的认识。炎症刺激的性质和严重程度以及患者的遗传和体质在这些疾病的糖皮质激素敏感性、依赖性和耐药性中起关键作用。尽管糖皮质激素会增加机会性感染的易感性,但在存在严重全身炎症时,如在脓毒性休克和急性呼吸窘迫综合征中观察到的那样,在疾病过程中持续给药时,它们也非常有益。糖皮质激素通过与免疫调节不同的分子机制产生其心血管、代谢和抗生长副作用。幸运的是,第一代组织和免疫与心血管/代谢效应选择性糖皮质激素可供研究和进一步改进。“设计型”糖皮质激素有望在炎症性疾病治疗方面取得重大新进展。

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