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类风湿关节炎患者外周血淋巴细胞 Tim-3 表达增加与疾病活动度呈负相关。

Increased Tim-3 expression on peripheral lymphocytes from patients with rheumatoid arthritis negatively correlates with disease activity.

机构信息

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.

出版信息

Clin Immunol. 2010 Nov;137(2):288-95. doi: 10.1016/j.clim.2010.07.012.

Abstract

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.

摘要

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。

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