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心理压力在体内对皮肤树突状细胞功能发挥辅助作用。

Psychological stress exerts an adjuvant effect on skin dendritic cell functions in vivo.

作者信息

Saint-Mezard Pierre, Chavagnac Cyril, Bosset Sophie, Ionescu Marius, Peyron Eric, Kaiserlian Dominique, Nicolas Jean-Francois, Bérard Frédéric

机构信息

Institut National de la Santé et de la Recherche Médicale Unité 503, IFR 128, and Department of Clinical Immunology and Allergy, CHU Lyon-Sud, Lyon, France.

出版信息

J Immunol. 2003 Oct 15;171(8):4073-80. doi: 10.4049/jimmunol.171.8.4073.

Abstract

Psychological stress affects the pathophysiology of infectious, inflammatory, and autoimmune diseases. However, the mechanisms by which stress could modulate immune responses in vivo are poorly understood. In this study, we report that application of a psychological stress before immunization exerts an adjuvant effect on dendritic cell (DC), resulting in increased primary and memory Ag-specific T cell immune responses. Acute stress dramatically enhanced the skin delayed-type hypersensitivity reaction to haptens, which is mediated by CD8(+) CTLs. This effect was due to increased migration of skin DCs, resulting in augmented CD8(+) T cell priming in draining lymph nodes and enhanced recruitment of CD8(+) T cell effectors in the skin upon challenge. This adjuvant effect of stress was mediated by norepinephrine (NE), but not corticosteroids, as demonstrated by normalization of the skin delayed-type hypersensitivity reaction and DC migratory properties following selective depletion of NE. These results suggest that release of NE by sympathetic nerve termini during a psychological stress exerts an adjuvant effect on DC by promoting enhanced migration to lymph nodes, resulting in increased Ag-specific T cell responses. Our findings may open new ways in the treatment of inflammatory diseases, e.g., psoriasis, allergic contact dermatitis, and atopic dermatitis.

摘要

心理应激会影响感染性、炎症性和自身免疫性疾病的病理生理学。然而,应激在体内调节免疫反应的机制却知之甚少。在本研究中,我们报告了在免疫接种前施加心理应激对树突状细胞(DC)具有佐剂效应,从而导致初次和记忆性抗原特异性T细胞免疫反应增强。急性应激显著增强了对半抗原的皮肤迟发型超敏反应,该反应由CD8(+)细胞毒性T淋巴细胞(CTL)介导。这种效应是由于皮肤DC迁移增加,导致引流淋巴结中CD8(+) T细胞致敏增强,以及在激发时皮肤中CD8(+) T细胞效应器的募集增加。应激的这种佐剂效应是由去甲肾上腺素(NE)介导的,而非皮质类固醇,选择性耗竭NE后皮肤迟发型超敏反应和DC迁移特性恢复正常即证明了这一点。这些结果表明,心理应激期间交感神经末梢释放的NE通过促进DC向淋巴结的迁移增强而对DC发挥佐剂效应,从而导致抗原特异性T细胞反应增加。我们的发现可能为治疗炎症性疾病,如银屑病、过敏性接触性皮炎和特应性皮炎开辟新途径。

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