Elrefaei Mohamed, Baker Chris A R, Jones Norman G, Bangsberg David R, Cao Huyen
California Department of Public Health, Richmond, CA 94804, USA.
J Immunol. 2008 Jun 1;180(11):7757-63. doi: 10.4049/jimmunol.180.11.7757.
Mechanisms leading to the observed immune dysregulation in HIV-1 infection are not well understood. HIV-specific IL-10-positive CD8(+) T cells are increased in advanced HIV disease. We have previously reported that Gag-specific IL-10-positive CD8(+) T cells suppressed cytolysis. In this study we describe the suppressive effect of Nef-specific IL-10-positive CD8(+) T cells. Interestingly, simultaneous removal of both Gag- and Nef-specific IL-10-positive CD8(+) T cells led to higher HIV-specific cytolysis compared with the removal of Nef-specific IL-10-positive CD8(+) T cells alone. We also examined the level of programmed cell death-1 (PD-1) as a measure of immune dysfunction in association with IL-10-positive suppressor CD8(+) T cells. The level of PD-1 expression on CD107-positive effector CD8(+) T cells was significantly increased when IL-10-positive suppressor CD8(+) T cells were present (p < 0.05). Our results suggest that IL-10-positive suppressor CD8(+) T cells contribute to the immune dysfunction observed in advanced HIV infection and that the concomitant presence of multiple IL-10-positive CD8(+) T cell populations may have an additive suppressive effect.
导致在HIV-1感染中观察到的免疫失调的机制尚未完全明确。在晚期HIV疾病中,HIV特异性白细胞介素-10阳性CD8(+) T细胞数量增加。我们之前报道过,Gag特异性白细胞介素-10阳性CD8(+) T细胞可抑制细胞溶解。在本研究中,我们描述了Nef特异性白细胞介素-10阳性CD8(+) T细胞的抑制作用。有趣的是,与单独去除Nef特异性白细胞介素-10阳性CD8(+) T细胞相比,同时去除Gag特异性和Nef特异性白细胞介素-10阳性CD8(+) T细胞会导致更高的HIV特异性细胞溶解。我们还检测了程序性细胞死亡蛋白1(PD-1)的水平,以此作为与白细胞介素-10阳性抑制性CD8(+) T细胞相关的免疫功能障碍的指标。当存在白细胞介素-10阳性抑制性CD8(+) T细胞时,CD107阳性效应性CD8(+) T细胞上的PD-1表达水平显著升高(p < 0.05)。我们的结果表明,白细胞介素-10阳性抑制性CD8(+) T细胞促成了晚期HIV感染中观察到的免疫功能障碍,并且多个白细胞介素-10阳性CD8(+) T细胞群体的同时存在可能具有累加抑制作用。