Department of Clinical laboratory, Qilu Hospital of Shandong University, Ji'nan, China.
Key Laboratory of Tumor Marker Translational Medicine, Shandong Provincial Medicine and Health, Ji'nan, China.
Autoimmunity. 2021 Mar;54(2):97-103. doi: 10.1080/08916934.2021.1891535. Epub 2021 Mar 1.
T cell immunoglobulin and mucin domain-containing molecule-3(Tim-3) has been found to play important roles in systemic lupus erythematosus (SLE), but whether sTim-3 is involved in the development of SLE remains unknown. In this study, we firstly observed an increased expression of plasma sTim-3 in SLE patients, especially active SLE patients. The plasma sTim-3 levels were positively correlated with anti-dsDNA, SLEDAI score, ESR, and urine albumin. The plasma sTim-3 levels were negatively correlated with C3 and C4. The area under the ROC curve (AUC) values indicated that the plasma sTim-3 level was significantly discriminative of early active SLE from stable SLE and HC with high sensitivity and specificity. The present results suggest that sTim-3 might serve as a potential biomarker for promising the disease activity of SLE.
T 细胞免疫球蛋白和黏蛋白结构域分子-3(Tim-3)已被发现在系统性红斑狼疮(SLE)中发挥重要作用,但可溶性 Tim-3 是否参与 SLE 的发生尚不清楚。本研究首次观察到 SLE 患者,尤其是活动期 SLE 患者血浆可溶性 Tim-3 表达增加。血浆 sTim-3 水平与抗 dsDNA、SLEDAI 评分、ESR 和尿白蛋白呈正相关,与 C3 和 C4 呈负相关。ROC 曲线下面积(AUC)值表明,血浆 sTim-3 水平可显著区分活动期 SLE 与稳定期 SLE 和 HC,具有较高的敏感性和特异性。本研究结果提示 sTim-3 可能作为一种有前途的 SLE 疾病活动的潜在生物标志物。