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[皮肤作为一种免疫系统]

[Skin as an immune system].

作者信息

Hunyadi J, Szabó I, Simon M

机构信息

Debreceni Orvostudományi Egyetem, Börgyógyászati Klinika.

出版信息

Orv Hetil. 1994 Dec 11;135(50):2749-54.

PMID:7838510
Abstract

Skin consists of three structurally and functionally distinct compartments containing resident and nonresident cells. These cells cooperative with humoral pathway of immune system in defence of healthy skin. Resident and nonresident cells are able to initiate inflammatory or immune processes of skin, although interstitial reactions (activation by bacteria, immunoglobulin or complement) also take place in such processes. In normal conditions nonresident cells can migrate through vascular endothel, however, PMN granulocytes and B lymphocytes cannot. Resident and nonresident cells of skin are capable of exerting a wide range of immunomodulatory effects, among them keratinocytes are of distinguished significance producing arachidon metabolites and IL-1 as well. Activated skin cells might induce chemotactic migration of distinct white blood cells normally absent or only a few cells being present in healthy skin. Cell migration into the interstitial space of skin is mediated by adhesion molecules expressed on cell surface of migrating cells, vascular endothel cells and on keratinocytes. Composition and density of adhesion molecules vary by type of stimuli, therefore various cytokines might induce distinct reactions mediated by certain population of cells. In addition, initiation and progress of immune- or inflammatory reactions are determined by the involved cell-populations as well. Normal regulation provides appropriate control and termination of the reaction, however, uncontrolled regulation results in development of pathological state.

摘要

皮肤由三个结构和功能不同的部分组成,包含常驻细胞和非常驻细胞。这些细胞与免疫系统的体液途径协同作用,以保护健康的皮肤。常驻细胞和非常驻细胞能够启动皮肤的炎症或免疫过程,尽管在此类过程中也会发生间质反应(由细菌、免疫球蛋白或补体激活)。在正常情况下,非常驻细胞可以穿过血管内皮,但中性粒细胞和B淋巴细胞则不能。皮肤的常驻细胞和非常驻细胞能够发挥广泛的免疫调节作用,其中角质形成细胞产生花生四烯酸代谢产物和白细胞介素-1也具有显著意义。活化的皮肤细胞可能会诱导不同白细胞的趋化性迁移,这些白细胞在健康皮肤中通常不存在或仅有少量存在。细胞迁移到皮肤间质空间是由迁移细胞、血管内皮细胞和角质形成细胞表面表达的粘附分子介导的。粘附分子的组成和密度因刺激类型而异,因此各种细胞因子可能会诱导由特定细胞群体介导的不同反应。此外,免疫或炎症反应的启动和进展也取决于所涉及的细胞群体。正常调节可对反应进行适当控制和终止,然而,不受控制的调节会导致病理状态的发展。

相似文献

1
[Skin as an immune system].[皮肤作为一种免疫系统]
Orv Hetil. 1994 Dec 11;135(50):2749-54.
2
IL-17 is produced by nickel-specific T lymphocytes and regulates ICAM-1 expression and chemokine production in human keratinocytes: synergistic or antagonist effects with IFN-gamma and TNF-alpha.白细胞介素-17由镍特异性T淋巴细胞产生,并调节人角质形成细胞中细胞间黏附分子-1的表达和趋化因子的产生:与γ干扰素和肿瘤坏死因子-α的协同或拮抗作用。
J Immunol. 1999 Jan 1;162(1):494-502.
3
Neutrophils migrate to delayed-type hypersensitivity reactions in joints, but not in skin. Mechanism is leukocyte function-associated antigen-1-/Mac-1-independent.中性粒细胞会迁移至关节的迟发型超敏反应部位,但不会迁移至皮肤的迟发型超敏反应部位。其机制与白细胞功能相关抗原-1/巨噬细胞-1无关。
J Immunol. 1994 Dec 15;153(12):5689-97.
4
A cytokine-to-chemokine axis between T lymphocytes and keratinocytes can favor Th1 cell accumulation in chronic inflammatory skin diseases.T淋巴细胞与角质形成细胞之间的细胞因子-趋化因子轴可促进Th1细胞在慢性炎症性皮肤病中的积聚。
J Leukoc Biol. 2001 Oct;70(4):617-23.
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Multistep navigation of Langerhans/dendritic cells in and out of the skin.朗格汉斯细胞/树突状细胞进出皮肤的多步骤导航。
J Allergy Clin Immunol. 2001 Nov;108(5):688-96. doi: 10.1067/mai.2001.118797.
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Dermatitis due to epiregulin deficiency and a critical role of epiregulin in immune-related responses of keratinocyte and macrophage.由表皮调节素缺乏引起的皮炎以及表皮调节素在角质形成细胞和巨噬细胞免疫相关反应中的关键作用。
Proc Natl Acad Sci U S A. 2004 Sep 21;101(38):13921-6. doi: 10.1073/pnas.0404217101. Epub 2004 Sep 13.
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House dust and storage mite extracts influence skin keratinocyte and fibroblast function.屋尘和储存螨提取物影响皮肤角质形成细胞和成纤维细胞的功能。
Int Arch Allergy Immunol. 2008;145(1):33-42. doi: 10.1159/000107464. Epub 2007 Aug 17.
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Skin homing of Langerhans cell precursors: adhesion, chemotaxis, and migration.朗格汉斯细胞前体的皮肤归巢:黏附、趋化作用和迁移
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Effects of contact allergens on human Langerhans cells in skin organ culture: migration, modulation of cell surface molecules, and early expression of interleukin-1 beta protein.接触性变应原对皮肤器官培养中人类朗格汉斯细胞的影响:迁移、细胞表面分子的调节以及白细胞介素-1β蛋白的早期表达
Lab Invest. 1996 Feb;74(2):422-36.
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