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细胞介导的免疫:白细胞介素-3和白细胞介素-6在接触性敏感反应调节中的作用

Cell-mediated immunity: role of IL-3 and IL-6 in the regulation of contact sensitivity reaction.

作者信息

Marcinkiewicz J

机构信息

Department of Immunology, Academy of Medicine, Kraków, Poland.

出版信息

Folia Histochem Cytobiol. 1990;28(3):107-19.

PMID:2096080
Abstract

Delayed type hypersensitivity reaction (DTH) consists of a sequential cascade of steps depending on different types of T cells, as well as mast cells, endothelial cells and macrophages. Recently it has been shown that CD4+ TH1 lymphocytes ("inflammatory type") play a central role in DTH reaction. Activated TH1 cells produce a characteristic pattern of cytokines: IL-2, IL-3, TNF-beta, IFN-gamma. Using the contact sensitivity (CS) reaction on mice as a model system, the role of cytokines in the regulation of DTH is presented, particularly the significance of IL-3 and IL-6. The recent data can be interpreted to show that IL-6 released by activated macrophages (APC cells) in the induction phase of the CS reaction probably stimulate CD8+ T suppressor cells. These in turn inhibit the production of IL-2 and IL-3 by CD4+ TH1 cells followed by a state of unresponsiveness.

摘要

迟发型超敏反应(DTH)由一系列连续的步骤组成,这取决于不同类型的T细胞,以及肥大细胞、内皮细胞和巨噬细胞。最近研究表明,CD4 + TH1淋巴细胞(“炎症型”)在DTH反应中起核心作用。活化的TH1细胞产生一组特征性的细胞因子:IL-2、IL-3、TNF-β、IFN-γ。以小鼠接触性敏感(CS)反应作为模型系统,阐述了细胞因子在DTH调节中的作用,特别是IL-3和IL-6的重要性。最近的数据可以解释为,在CS反应诱导阶段由活化巨噬细胞(APC细胞)释放的IL-6可能刺激CD8 + T抑制细胞。这些细胞继而抑制CD4 + TH1细胞产生IL-2和IL-3,随后进入无反应状态。

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