Ford Mandy L, Adams Andrew B, Pearson Thomas C
The Emory Transplant Center, Emory University, 101 Woodruff Circle, Woodruff Memorial Research Building Suite 5105, Atlanta, GA 30322, USA.
Nat Rev Nephrol. 2014 Jan;10(1):14-24. doi: 10.1038/nrneph.2013.183. Epub 2013 Oct 8.
The myriad of co-stimulatory signals expressed, or induced, upon T-cell activation suggests that these signalling pathways shape the character and magnitude of the resulting autoreactive or alloreactive T-cell responses during autoimmunity or transplantation, respectively. Reducing pathological T-cell responses by targeting T-cell co-stimulatory pathways has met with therapeutic success in many instances, but challenges remain. In this Review, we discuss the T-cell co-stimulatory molecules that are known to have critical roles during T-cell activation, expansion, and differentiation. We also outline the functional importance of T-cell co-stimulatory molecules in transplantation, tolerance and autoimmunity, and we describe how therapeutic blockade of these pathways might be harnessed to manipulate the immune response to prevent or attenuate pathological immune responses. Ultimately, understanding the interplay between individual co-stimulatory and co-inhibitory pathways engaged during T-cell activation and differentiation will lead to rational and targeted therapeutic interventions to manipulate T-cell responses and improve clinical outcomes.
T细胞活化时表达或诱导的众多共刺激信号表明,这些信号通路分别在自身免疫或移植过程中塑造了产生的自身反应性或同种异体反应性T细胞反应的特征和强度。在许多情况下,通过靶向T细胞共刺激通路来减少病理性T细胞反应已取得治疗成功,但挑战依然存在。在本综述中,我们讨论了已知在T细胞活化、扩增和分化过程中起关键作用的T细胞共刺激分子。我们还概述了T细胞共刺激分子在移植、耐受性和自身免疫中的功能重要性,并描述了如何利用对这些通路的治疗性阻断来操纵免疫反应,以预防或减轻病理性免疫反应。最终,了解T细胞活化和分化过程中各个共刺激和共抑制通路之间的相互作用,将带来合理且有针对性的治疗干预措施,以操纵T细胞反应并改善临床结果。