Vu Minh Diem, Li Xian Chang
Department of Medicine, Harvard Medical School, Division of Immunology, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
Arch Immunol Ther Exp (Warsz). 2004 Jul-Aug;52(4):267-73.
Transplant rejection, like tolerance, is a T cell-dependent event. There is compelling evidence to suggest that induction of transplant tolerance is an actively learned process in which T cells need to engage the alloantigens in order to learn to tolerate the allograft. A family of cytokines whose receptors use the same IL-2 receptor gamma chain (also called the common gammac) plays an important role in regulating multiple aspects of the allograft response (i.e. rejection vs. tolerance). It is undeniable that gammac-cytokines can drive clonal expansion and effector maturation of alloreactive T cells, and therefore, targeting such cytokines or their receptor components remains an attractive way of blocking transplant rejection. However, we just started to appreciate that gammac-cytokines also regulate the acquisition of transplant tolerance via programming activated T cells for apoptotic cell death and via guiding the evolution of regulatory T cells. Thus, understanding precisely the role of gammac-cytokines in regulating T cell homeostasis and T cell regulation is critically important in the induction of transplant tolerance.
移植排斥反应与免疫耐受一样,是一个依赖T细胞的过程。有确凿证据表明,诱导移植耐受是一个主动学习的过程,在此过程中T细胞需要接触同种异体抗原才能学会耐受同种异体移植物。一类细胞因子的受体使用相同的IL-2受体γ链(也称为共同γ链),在调节同种异体移植反应的多个方面(即排斥与耐受)中发挥重要作用。不可否认,γ链细胞因子可驱动同种异体反应性T细胞的克隆扩增和效应细胞成熟,因此,靶向此类细胞因子或其受体成分仍然是阻断移植排斥反应的一种有吸引力的方法。然而,我们刚刚开始认识到,γ链细胞因子还通过对活化T细胞进行凋亡性细胞死亡编程以及引导调节性T细胞的演变来调节移植耐受的获得。因此,准确理解γ链细胞因子在调节T细胞稳态和T细胞调节中的作用对于诱导移植耐受至关重要。