Expression of human T cell immunoglobulin domain and mucin-3 (TIM-3) on kidney tissue from systemic lupus erythematosus (SLE) patients
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  • 作者:Ling Guo (1)
    Xiangdong Yang (1)
    Qing Xia (1)
    Junhui Zhen (2)
    Xuewei Zhuang (3)
    Tao Peng (1)
  • 关键词:Human T cell immunoglobulin domain and mucin ; 3 (TIM ; 3) ; Systemic lupus erythematosus (SLE) ; Expression
  • 刊名:Clinical and Experimental Medicine
  • 出版年:2014
  • 出版时间:November 2014
  • 年:2014
  • 卷:14
  • 期:4
  • 页码:383-388
  • 全文大小:720 KB
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    5. Pan HF, Zhang N, Li WX, Tao JH, Ye DQ (2010) TIM-3 as a new therapeutic target in systemic lupus erythematosus. Mol Biol Rep 37(1):395-98 CrossRef
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  • 作者单位:Ling Guo (1)
    Xiangdong Yang (1)
    Qing Xia (1)
    Junhui Zhen (2)
    Xuewei Zhuang (3)
    Tao Peng (1)

    1. Department of Nephrology, Shandong University Qilu Hospital, Jinan, 250012, China
    2. Department of Pathology, Shandong University Qilu Hospital, Jinan, China
    3. Department of Clinical Laboratory Medicine, Shandong University Qilu Hospital, Jinan, China
  • ISSN:1591-9528
文摘
The aim of this study was to evaluate the expression of TIM-3 in renal tissue from patients with systemic lupus erythematosus (SLE) and patients without SLE, and to evaluate the difference of TIM-3 expression between them. A total of 272 patients with SLE as SLE group and 62 patients without SLE as control group were enrolled in the present study. Patients with SLE accepted percutaneous renal biopsy. We examined the expression of TIM-3 in renal tissue and the serological parameters in serum from all enrolled cases. The expression of TIM-3 and serological parameters were compared between the different groups. Positive staining of TIM-3 protein was seen in 97.1?% patients with SLE (264 out of 272), but 95.2?% negative staining in the cases without SLE (59 out of 62), only 3 out of 62 patients in control group were positive staining of TIM-3. There were significant differences between two groups in almost all serological markers which reflect SLE activity. There was a nearly positive correlation between pathological manifestations and expression degree of TIM-3. High immuno-reactivity of TIM-3 was found to be significantly correlated with serological grade (p?

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