Institute of Immunology, Key Laboratory for Experimental Teratology of Ministry of Education, Shandong University School of Medicine, 44# Wenhua Xi Road, Jinan, Shandong, 250012, PR China.
Clin Immunol. 2010 Nov;137(2):288-95. doi: 10.1016/j.clim.2010.07.012.
Tim-3 has been reported as an important regulatory molecule and plays a pivotal role in several autoimmunity diseases. Here, we demonstrated the increased expression of Tim-3 on peripheral CD4(+) T, CD8(+) T, NKT cells and monocytes from RA patients compared to those from healthy controls. Percentage of Tim-3(+) cells in peripheral blood mononuclear cells (PBMCs) showed an inverse correlation with disease activity score 28 (DAS28) and plasma TNF-α level. Similar negative correlations were found between disease activity and Tim-3 levels on CD4(+) T, CD8(+) T and NKT cells. Consistently, Tim-3 expression on CD3(+) T cells was further increased in patients with disease remission after treatment. Tim-3 expression on CD8(+) T and NKT cells negatively correlates with plasma TNF-α. Our results suggest that Tim-3 might participate in the proceeding of RA by its negative regulation on various T cell subsets. Tim-3 might be a potential new marker for assessing severity of RA.
Tim-3 被报道为一个重要的调节分子,在几种自身免疫性疾病中发挥关键作用。在这里,我们发现在 RA 患者的外周血 CD4(+)T、CD8(+)T、NKT 细胞和单核细胞中,Tim-3 的表达增加,与健康对照组相比。外周血单个核细胞(PBMCs)中 Tim-3(+)细胞的百分比与疾病活动评分 28(DAS28)和血浆 TNF-α水平呈负相关。在 CD4(+)T、CD8(+)T 和 NKT 细胞上,疾病活动与 Tim-3 水平之间也存在类似的负相关关系。一致地,在治疗后疾病缓解的患者中,CD3(+)T 细胞上的 Tim-3 表达进一步增加。CD8(+)T 和 NKT 细胞上的 Tim-3 表达与血浆 TNF-α呈负相关。我们的结果表明,Tim-3 可能通过对各种 T 细胞亚群的负调节参与 RA 的发生。Tim-3 可能是评估 RA 严重程度的一个潜在的新标志物。