Circulating IL-35 in pancreatic ductal adenocarcinoma patients

被引:70
作者
Jin, Peng [1 ]
Ren, He [1 ]
Sun, Wei [1 ]
Xin, Wen [1 ]
Zhang, Huan [1 ]
Hao, Jihui [1 ]
机构
[1] Tianjin Med Univ, Tianjin Canc Hosp, Key Lab Canc Treatment & Prevent, Dept Pancreat Canc, Tianjin 300060, Peoples R China
基金
中国国家自然科学基金;
关键词
REGULATORY T-CELLS; EPSTEIN-BARR-VIRUS; INDUCED GENE 3; INDUCED ARTHRITIS; TREG CELLS; CYTOKINE; INTERLEUKIN-35; MICROENVIRONMENT; INFLAMMATION; SUPPRESSION;
D O I
10.1016/j.humimm.2013.09.018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-35 is a novel inhibitory cytokine that is mainly produced by regulatory T-cells (Tregs) and is required for Treg-mediated immunosuppression. However, the plasma levels of IL-35 in patients with pancreatic ductal adenocarcinoma (PDAC) have never been investigated. In this study, we found that plasma IL-35 levels more significantly increased in PDAC patients than in normal controls (134.53 +/- 92.45 pg/mL vs. 14.26 +/- 6.56 pg/mL). IL-35 mRNA levels were positively correlated with plasma IL-35 levels (EBI3, R = 0.925, p < 0.01; p35, R = 0.916, p < 0.01). Furthermore, IL-35 expression levels were associated with lymph node metastasis (p = 0.001) and late tumor stage (p = 0.002). For the resected patients, high IL-35 expression levels were associated with large tumor size (p < 0.01), higher TNM classification T staging (p < 0.05), and late tumor stage (p < 0.05). In conclusion, circulating IL-35 in PDAC patients significantly increased, suggesting that regulating the expression of IL-35 may provide a new possible target for the treatment of PDAC patients, especially for the resectable ones. (C) 2013 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:29 / 33
页数:5
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