Raman Chander
Department of Medicine, University of Alabama at Birmingham, 35294-0007, USA.
Immunol Res. 2002;26(1-3):255-63. doi: 10.1385/IR:26:1-3:255.
The CD5 coreceptor is a cysteine-rich scavenger receptor family glycoprotein that is expressed constitutively on all T cells and a subset of B cells (B I a B cells). It is now generally accepted that the biologic role of CD5 is to regulate intracellular strength induced by antigen receptors in both T and B cells. However, at present it is unclear if this coreceptor's effect on antigen receptor signaling is primarily costimulatory or inhibitory since support for both exists. Our studies focus on understanding the physiologic role of CD5 in the context of regulation of antigen receptor activation, B and T cell selection, and generation/maintenance of immune tolerance. In this overview, I discuss studies using experimental models of lymphocyte selection and tolerance showing that CD5 plays a key role in B and T cell selection as well as generation and maintenance of tolerance. I and others, reviewed here, now provide clear evidence that CD5 is a key regulator of immune tolerance and that alterations of its activity can promote development of autoreactivity.
CD5共受体是一种富含半胱氨酸的清道夫受体家族糖蛋白,在所有T细胞和一部分B细胞(B I a B细胞)上组成性表达。目前普遍认为,CD5的生物学作用是调节T细胞和B细胞中抗原受体诱导的细胞内信号强度。然而,目前尚不清楚这种共受体对抗原受体信号传导的影响主要是共刺激还是抑制,因为两者都有相关支持证据。我们的研究重点是了解CD5在调节抗原受体激活、B细胞和T细胞选择以及免疫耐受的产生/维持方面的生理作用。在本综述中,我讨论了使用淋巴细胞选择和耐受实验模型的研究,这些研究表明CD5在B细胞和T细胞选择以及耐受的产生和维持中起关键作用。我和其他在此处被综述的研究者,现在提供了明确的证据表明CD5是免疫耐受的关键调节因子,其活性改变可促进自身反应性的发展。