Dysregulation of Circulating Follicular Helper T Cells in Nonsmall Cell Lung Cancer

被引:28
作者
Shi, Weiwei [1 ]
Li, Xiaoyan [2 ]
Cha, Zhanshan [3 ]
Sun, Shengjie [1 ]
Wang, Lijie [1 ]
Jiao, Shunchang [1 ]
Yang, Bo [1 ]
Shi, Yan [1 ]
Wang, Zhikuan [1 ]
Wu, Zhiyong [1 ]
Dai, Guanghai [1 ]
机构
[1] Peoples Liberat Army Gen Hosp, Dept Oncol, Beijing 100853, Peoples R China
[2] Acad Mil Med Sci, PLA, Affiliated Hosp, Dept Lung Canc, Beijing, Peoples R China
[3] Second Mil Med Univ, Changhai Hosp, Dept Transfus, Shanghai, Peoples R China
关键词
LYMPHOMA; EXPRESSION; ICOS; FH; SUBSETS; FOXP3;
D O I
10.1089/dna.2013.2332
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nonsmall cell lung cancer (NSCLC) is greatly affected by the dysregulation of the immune system. Circulating follicular helper T cells (Tfh) play critical roles in inducing B-cell activation and producing various cytokines. In the current study, we investigated levels of circulating Tfh in NSCLC. Circulating Tfh and it subtypes were determined by measuring CD3, CD4, CXCR5, CXCR3, and CCR6 in 62 NSCLC patients and 66 healthy controls using flow cytometry. Data presented that percentage of circulating Tfh in the peripheral CD4(+) T cells was significantly increased in NSCLC (14.0%) than in controls (8.7%) (p < 0.001). Further analysis revealed that the upregulation of Tfh was contributed by the Th2-Tfh subtype and the Th17-Tfh subtype, whereas the percentage of the Th1-Tfh subtype was significantly decreased in patients. Investigating the clinical stages of the patients demonstrated that prevalence of Tfh was significantly elevated in cases with advanced stages (III: 14.2%; IV: 16.4%) than those with primary stages (I: 10.9%; II: 10.8%). In addition, we analyzed Tfh in patients with different histological types. Results showed that the percentage of circulating Tfh was further upregulated in adenocarcima than squamous cell carcinoma or other types. This study suggests the involvement of circulating Tfh in the pathogenesis and progression of NSCLC, and provides a potential pathway for understanding this disease.
引用
收藏
页码:355 / 360
页数:6
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