Elevated Expression of Programmed Death-1 and Programmed Death Ligand-1 Negatively Regulates Immune Response against Cervical Cancer Cells

被引:29
|
作者
Chen, Zhifang [1 ]
Pang, Nannan [2 ]
Du, Rong [1 ]
Zhu, Yuejie [1 ]
Fan, Lingling [1 ]
Cai, Donghui [1 ]
Ding, Yan [1 ]
Ding, Jianbing [3 ]
机构
[1] Xinjiang Med Univ, Dept Gynecol, Affiliated Hosp 1, Urumqi 830054, Peoples R China
[2] Xinjiang Med Univ, Dept Hematol, Affiliated Hosp 1, Urumqi 830054, Peoples R China
[3] Xinjiang Med Univ, Dept Immunol, Urumqi 830011, Peoples R China
基金
中国博士后科学基金;
关键词
LUNG-CANCER; HUMAN-PAPILLOMAVIRUS; INTRAEPITHELIAL NEOPLASIA; ANTI-PD-1; THERAPY; PD-L1; EXPRESSION; TGF-BETA; IMMUNOTHERAPY; CARCINOMA; BLOCKADE; MICROENVIRONMENT;
D O I
10.1155/2016/6891482
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The present study is to measure the expression of programmed death-1 (PD-1) and programmed death ligand-1 (PD-L1), as well as its clinical significance in cervical cancer patients. Our results showed that different T cell subsets in patients with cervical cancer had high expression of PD-1, and DCs had high expression of PD-L1. High expression of PD-1 on Treg cells in cervical cancer patients facilitated the production of TGF-beta and IL-10 but inhibited the production of IFN-gamma Cervical cancer elevated the expression of PD-1 and PD-L1 in mRNA level. PD-1 expression in peripheral blood of cervical cancer patients was related with tumor differentiation, lymph node metastasis, and invasiveness. PD-1/PD-L1 pathway inhibited lymphocyte proliferation but enhanced the secretion of IL-10 and TGF-beta in vitro. In summary, our findings demonstrate that elevated levels of PD-1/PD-L1, TGF-beta and IL-10 in peripheral blood of cervical cancer patients may negatively regulate immune response against cervical cancer cells and contribute to the progression of cervical cancer. Therefore, PD-1/PD-L1 pathway may become an immunotherapy target in the future.
引用
收藏
页数:11
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