Niewold Timothy B, Clark Daniel N, Salloum Rafah, Poole Brian D
Section of Rheumatology and Gwen Knapp Center for Lupus and Immunology Research, The University of Chicago, Chicago, IL 60637, USA.
J Biomed Biotechnol. 2010;2010:948364. doi: 10.1155/2010/948364. Epub 2010 Jun 29.
The pleiotropic cytokine interferon alpha is involved in multiple aspects of lupus etiology and pathogenesis. Interferon alpha is important under normal circumstances for antiviral responses and immune activation. However, heightened levels of serum interferon alpha and expression of interferon response genes are common in lupus patients. Lupus-associated autoantibodies can drive the production of interferon alpha and heightened levels of interferon interfere with immune regulation. Several genes in the pathways leading to interferon production or signaling are associated with risk for lupus. Clinical and cellular manifestations of excess interferon alpha in lupus combined with the genetic risk factors associated with interferon make this cytokine a rare bridge between genetic risk and phenotypic effects. Interferon alpha influences the clinical picture of lupus and may represent a therapeutic target. This paper provides an overview of the cellular, genetic, and clinical aspects of interferon alpha in lupus.
多效性细胞因子α干扰素参与狼疮病因学和发病机制的多个方面。在正常情况下,α干扰素对于抗病毒反应和免疫激活很重要。然而,狼疮患者血清中α干扰素水平升高以及干扰素反应基因的表达很常见。狼疮相关自身抗体可驱动α干扰素的产生,而α干扰素水平升高会干扰免疫调节。导致干扰素产生或信号传导途径中的几个基因与狼疮风险相关。狼疮中过量α干扰素的临床和细胞表现,以及与干扰素相关的遗传风险因素,使这种细胞因子成为遗传风险和表型效应之间罕见的桥梁。α干扰素影响狼疮的临床表现,可能代表一个治疗靶点。本文概述了狼疮中α干扰素的细胞、遗传和临床方面。