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α干扰素与炎症和免疫

Interferon-alpha in inflammation and immunity.

作者信息

Kaser A, Tilg H

机构信息

Department of Medicine, University Hospital Innsbruck, Austria.

出版信息

Cell Mol Biol (Noisy-le-grand). 2001 Jun;47(4):609-17.

Abstract

Type I interferons, constituting IFN-alpha and IFN-beta, were initially described for their ability to interfere with viral replication. IFN-alpha was the first cytokine to be cloned and used successfully as a therapeutic cytokine, although its mechanism of action remained largely elusive. Evidence gathered over the last few years shed light on the molecular effects of IFN-alpha, especially its interaction with the cytokine cascade. Recently, the principle source of IFN-alpha could be identified as the precursor of type 2 dendritic cells, and IFN-alpha has been identified as the cytokine linking innate with adaptive immunity via its interaction with dendritic cells.

摘要

I型干扰素由IFN-α和IFN-β组成,最初因其干扰病毒复制的能力而被描述。IFN-α是第一个被克隆并成功用作治疗性细胞因子的细胞因子,尽管其作用机制在很大程度上仍不清楚。过去几年收集的证据揭示了IFN-α的分子效应,特别是其与细胞因子级联反应的相互作用。最近,IFN-α的主要来源可被确定为2型树突状细胞的前体,并且IFN-α已被确定为通过其与树突状细胞的相互作用将先天性免疫与适应性免疫联系起来的细胞因子。

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