Carl Joseph W, Bai Xue-Feng
Department of Pathology and Comprehensive Cancer Center, The Ohio State University Medical Center Columbus, OH, USA.
Int J Clin Exp Pathol. 2008 Jan 1;1(2):117-23.
IL27 is the newest member of the IL6/IL12 family. It consists of Epstein-Barr virus-induced gene 3 (EBI3) and p28 subunits and signals through the IL27 receptor complex formed by WSX-1 and gp130 subunits. IL27-IL27 receptor interaction was initially shown to induce an early signal for the induction of Th1 responses. Recently other studies indicate that IL27 inhibits inflammatory Th17 lineage development. Despite the overall effects observed, the role of individual IL27 subunits remains controversial and is largely unclear. EBI3, while predominately found with p28 to form IL27, has different expression kinetics than p28. P28 has also been shown to signal independently of EBI3. Moreover, EBI3 has other potential binding partners such as the p35 subunit of IL12 and theoretically may regulate the inflammatory response through yet undiscovered mechanisms. Understanding the inflammatory and anti-inflammatory roles of IL27 and its subunits are essential before the immunological regulatory therapies can be developed.
白细胞介素27(IL27)是白细胞介素6/白细胞介素12家族的最新成员。它由爱泼斯坦-巴尔病毒诱导基因3(EBI3)和p28亚基组成,并通过由WSX-1和gp130亚基形成的IL27受体复合物发出信号。最初显示IL27与IL27受体的相互作用可诱导Th1反应的早期信号。最近的其他研究表明,IL27可抑制炎性Th17谱系的发育。尽管观察到了总体效果,但单个IL27亚基的作用仍存在争议且在很大程度上尚不清楚。EBI3虽然主要与p28一起形成IL27,但其表达动力学与p28不同。p28也已显示可独立于EBI3发出信号。此外,EBI3还有其他潜在的结合伙伴,如IL12的p35亚基,理论上可能通过尚未发现的机制调节炎症反应。在开发免疫调节疗法之前,了解IL27及其亚基的促炎和抗炎作用至关重要。