Integrated Department of Immunology, National Jewish Health and the University of Colorado School of Medicine, Denver, CO 80206, USA.
Immunol Res. 2013 Mar;55(1-3):3-9. doi: 10.1007/s12026-012-8344-0.
The innate immune response plays a critical role in pathogen clearance. However, dysregulation of innate immunity contributes to acute inflammatory diseases such as sepsis and many chronic inflammatory diseases including asthma, arthritis, and Crohn's disease. Pathogen recognition receptors including the Toll-like family of receptors play a pivotal role in the initiation of inflammation and in the pathogenesis of many diseases with an inflammatory component. Studies over the last 15 years have identified complex innate immune signal transduction pathways involved in inflammation that have provided many new potential therapeutic targets to treat disease. We are investigating several novel genes that exert spatial and in some cases temporal regulation on innate immunity signaling pathways. These novel genes include Tbc1d23, a RAB-GAP that inhibits innate immunity. In this review, we will discuss inflammation, the role of inflammation in disease, innate immune signal transduction pathways, and the use of spatiotemporal regulators of innate immunity as potential targets for discovery and therapeutics.
先天免疫反应在病原体清除中起着关键作用。然而,先天免疫失调会导致急性炎症性疾病,如败血症,以及许多慢性炎症性疾病,包括哮喘、关节炎和克罗恩病。病原体识别受体,包括 Toll 样受体家族,在炎症的启动和许多具有炎症成分的疾病的发病机制中起着关键作用。在过去的 15 年中,研究已经确定了涉及炎症的复杂先天免疫信号转导途径,为治疗疾病提供了许多新的潜在治疗靶点。我们正在研究几个新的基因,这些基因对先天免疫信号通路具有空间和在某些情况下时间上的调节作用。这些新的基因包括 Tbc1d23,一种抑制先天免疫的 RAB-GAP。在这篇综述中,我们将讨论炎症、炎症在疾病中的作用、先天免疫信号转导途径,以及先天免疫时空调节剂作为发现和治疗的潜在靶点的应用。