Department of Internal Medicine, Washington University School of Medicine, St Louis, Missouri 63110, USA.
Cold Spring Harb Perspect Biol. 2010 Aug;2(8):a002436. doi: 10.1101/cshperspect.a002436. Epub 2010 Jun 9.
CD28 costimulation regulates a wide range of cellular processes, from proliferation and survival to promoting the differentiation of specialized T-cell subsets. Since first being identified over 20 years ago, CD28 has remained a subject of intense study because of its profound consequences on T cell function and its potential for therapeutic manipulation. In this review we highlight the signaling cascades initiated by the major signaling motifs in CD28, focusing on PI-3 kinase-dependent and -independent pathways and how these are linked to specific cellular outcomes. Recent studies using gene targeted knockin mice have clarified the relative importance of these motifs on in vivo immune responses; however, much remains to be elucidated. Understanding the mechanism behind costimulation holds great potential for development of new clinically relevant reagents, a fact beginning to be realized with the advent of drugs that prevent CD28 ligation and signaling.
CD28 共刺激调节广泛的细胞过程,从增殖和存活到促进特定 T 细胞亚群的分化。自从 20 多年前首次被发现以来,CD28 一直是一个研究热点,因为它对 T 细胞功能有深远的影响,并且具有治疗干预的潜力。在这篇综述中,我们强调了 CD28 中主要信号基序引发的信号级联,重点关注 PI-3 激酶依赖性和非依赖性途径,以及这些途径如何与特定的细胞结果相关联。最近使用基因靶向敲入小鼠的研究阐明了这些基序在体内免疫反应中的相对重要性;然而,仍有许多问题需要阐明。了解共刺激背后的机制具有开发新的临床相关试剂的巨大潜力,这一事实随着阻止 CD28 连接和信号的药物的出现开始得到实现。