Th1-和th2型细胞因子调节趋化因子的表达。

S L Kunkel
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引用次数: 31

摘要

各种白细胞聚集到受伤和炎症组织的区域是最基本的宿主防御反应之一。历史证据支持这样一个概念,即急性炎症的病理特征是中性粒细胞的激发,而更多慢性炎症反应的白细胞组成本质上是单核的。有趣的是,关于从急性中性粒细胞介导的反应到慢性单核细胞导向的免疫反应的“转换”机制知之甚少。最近的研究表明,趋化因子的两个超基因家族在决定适当炎症反应所需的特定白细胞群的募集中起关键作用。特定趋化因子的表达似乎受到其他细胞因子的控制,如白细胞介素-1、-4和-10以及肿瘤坏死因子,它们在趋化因子的产生中充当正调节或负调节介质,从而控制白细胞亚群的募集。
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Th1- and Th2-type cytokines regulate chemokine expression.

The recruitment of various leukocyte populations to an area of injured and inflamed tissue is one of the most fundamental host defense responses. Historic evidence supports the concept that the pathology of acute inflammation is characterized by the elicitation of neutrophils, while the leukocyte composition of more chronic inflammatory responses is mononuclear in nature. Interestingly, little is known regarding the mechanism involved in the "switch' from an acute neutrophil-mediated response to a chronic mononuclear-cell-directed immune reaction. Recent studies demonstrate that two supergene families of chemokines play a key role in dictating the recruitment of specific leukocyte populations necessary for the appropriate inflammatory response. The expression of specific chemokines appears to be under the control of other cytokines, such as interleukins-1, -4 and -10, and tumor necrosis factor, that serve as either positive or negative regulatory mediators in the control of chemokine production, thus, controlling the recruitment of leukocyte subpopulations.

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