Yang Gui-lin, Xu Liu-mei, Yao Hong-yan, Wang Huo-sheng, Jiang Xiao-lin, Li Wei, Wang Min, Zhou Bo-ping
The Third People's Hospital of Shenzhen, Shenzhen Guangdong 518020, China.
Zhonghua Gan Zang Bing Za Zhi. 2009 Nov;17(11):831-4.
To investigate whether the CD4+CD25+Foxp3+ regulatory T cells are associated with serum TGF beta 1 in patients with hepatitis B.
Patients with chronic hepatitis B (CHB), chronic asymptomatic carriers (AsC), normal subjects (NS) and the resolved from HBV infection (Resolved) were recruited in this study. Flow cytometric analysis was used to detect the frequency and phenotype of peripheral CD4+CD25+Foxp3+ T cells, and Foxp3 gene expression were examined by real time PCR. Serum TGF beta 1 levels were measured by ELISA (enzyme-linked immunosorbent assay).
Patients with CHB or AsC exhibited significantly higher frequency of CD4+CD25+Foxp3+ T cells compared to healthy controls. CD4+CD25+ T cells derived from patients with CHB and AsC expressed higher level of Foxp3-mRNA. Furthermore, the frequency of CD4+CD25+Foxp3+ regulatory T cells was correlated with serum HBV DNA copy numbers in patients with CHB and AsC. Our results indicated that the serum TGF beta was increased in CHB and AsC patients compared to control patients, and that serum TGF beta was correlated with the expression of Foxp3-mRNA and the frequency of CD4+CD25+Foxp3+ regulatory T cells in patients with CHB and AsC.
The findings have important implication in the understanding of the role and mechanism of aberrant CD4+CD25+Foxp3+ regulatory T cells in the maintenance of chronicity in hepatitis B patients.
探讨慢性乙型肝炎患者CD4+CD25+Foxp3+调节性T细胞与血清转化生长因子β1(TGFβ1)是否相关。
本研究纳入慢性乙型肝炎(CHB)患者、慢性无症状携带者(AsC)、正常对照者(NS)及乙肝病毒感染已康复者(Resolved)。采用流式细胞术分析检测外周血CD4+CD25+Foxp3+T细胞的频率及表型,通过实时聚合酶链反应检测Foxp3基因表达。采用酶联免疫吸附测定法(ELISA)检测血清TGFβ1水平。
与健康对照相比,CHB患者或AsC患者的CD4+CD25+Foxp3+T细胞频率显著更高。CHB患者和AsC患者来源的CD4+CD25+T细胞表达更高水平的Foxp3 - mRNA。此外,CHB患者和AsC患者中,CD4+CD25+Foxp3+调节性T细胞的频率与血清乙肝病毒DNA拷贝数相关。我们的结果表明,与对照患者相比,CHB患者和AsC患者的血清TGFβ升高,且血清TGFβ与CHB患者和AsC患者中Foxp3 - mRNA的表达及CD4+CD25+Foxp3+调节性T细胞的频率相关。
这些发现对于理解异常的CD4+CD25+Foxp3+调节性T细胞在慢性乙型肝炎患者病情迁延中的作用及机制具有重要意义。