Increased circulating Th17 cell populations in patients with pancreatic ductal adenocarcinoma

被引:0
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作者
Imteyaz Ahmad Khan
Nidhi Singh
Deepak Gunjan
Srikant Gopi
Nihar Ranjan Dash
Surabhi Gupta
Anoop Saraya
机构
[1] Department of Gastroenterology and Human Nutrition Unit,
[2] All India Institute of Medical Sciences,undefined
[3] Department of Gastrointestinal Surgery,undefined
[4] All India Institute of Medical Sciences,undefined
[5] Department of Reproductive Biology,undefined
[6] All India Institute of Medical Sciences,undefined
来源
Immunogenetics | 2023年 / 75卷
关键词
Th17 cell; IL-17A; IL-23; Pancreatic ductal adenocarcinoma; Chronic pancreatitis;
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学科分类号
摘要
T-helper 17 (Th17) cells are a subset of CD4+ helper T cells that produce interleukin 17 (IL-17) and play a crucial role in the pathogenesis of inflammatory and autoimmune diseases. Few studies have been conducted to determine the role of Th17 cells in the tumorigenesis and development of pancreatic ductal adenocarcinoma (PDAC); however, its role is still unclear. In this study, the percentage of circulating Th17 cells and serum levels of IL-17A and IL-23 were analyzed using flow cytometry and ELISA, respectively, in 40 PDAC patients, 30 chronic pancreatitis (CP) patients and 30 healthy controls (HC). In addition, the mRNA expression levels of IL-17A, STAT3 and RORγt in tissue samples were quantified by qRT-PCR. The results showed that the percentage of circulating Th17 cells and the concentrations of serum IL-17A and IL-23 were significantly increased in PDAC patients as compared to CP and HC (P < 0.001). In addition, the higher level of IL-17A was significantly correlated with the poor overall survival of the PDAC patients. Furthermore, the frequencies of Th17 cells and IL-17A were significantly higher in stage III+IV PDAC patients versus stage I+II. A significant increase in IL-17A, STAT3 and RORγT mRNA was observed in patients with PDAC. Taken together, these findings suggest that the increased circulating Th17 cells and serum IL-17A may be involved in the development and metastasis of PDAC, and thus represent potential targets for the treatment of PDAC.
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页码:433 / 443
页数:10
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