State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Department of Infectious Diseases, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, P R of China.
Virol J. 2010 Aug 31;7:207. doi: 10.1186/1743-422X-7-207.
Accumulating evidence supports the theory that expression of CD127 on CD8 T cells during the process of antiviral immune response indicates a subset of effect CD8 T cells that successfully develop into fully protective memory. CD8 T cells expression of CD127 may be used as a predictor to evaluate disease status in chronic viral infection. The aim of this study was to investigate the CD127 expression level on different subsets of CD8 T cell and explore the relationship between CD127 expression on CD8 memory T cells and serum hepatitis B virus (HBV) DNA and hepatitis B e antigen (HBeAg) levels in patients with chronic hepatitis B (CHB). We also aimed to investigate the CD127 expression pattern on CD8 memory T cells of CHB patients who were treated with Telbivudine.
METHODS/RESULTS: Twenty HBeAg-positive CHB patients were selected and treated with telbivudine 600 mg/day for 48 weeks. The memory CD8 T cells were characterized by expression of CD45RA and CD27 markers. CD127 expression on the CD8 T-cell surface was measured by four-colour flow cytometry. Our results showed that CD127 expression on memory CD8 T cells was reduced in CHB patients. There was a strong negative correlation between CD127 expression on memory CD8 T cells and serum HBV DNA and HBeAg levels in CHB patients. Moreover, successful antiviral therapy increased CD127 expression on CD8 memory T cells as well as on HBV-specific CD8 T cells in CHB patients.
These results suggest that diminished CD127 expression on CD8 memory T cells of CHB patients is a potential mechanism explaining cellular immune function impairment in CHB infection, and that CD127 expression on CD8 memory T cells is a useful indicator for evaluating the effects of anti-HBV therapy.
越来越多的证据支持这样一种理论,即在抗病毒免疫反应过程中 CD8 T 细胞上 CD127 的表达表明了一组成功发展为完全保护性记忆的效应 CD8 T 细胞。CD8 T 细胞 CD127 的表达可作为评估慢性病毒感染中疾病状态的预测因子。本研究旨在调查 CD8 T 细胞不同亚群上 CD127 的表达水平,并探讨慢性乙型肝炎(CHB)患者中 CD8 记忆 T 细胞上 CD127 的表达与血清乙型肝炎病毒(HBV)DNA 和乙型肝炎 e 抗原(HBeAg)水平之间的关系。我们还旨在研究接受替比夫定治疗的 CHB 患者 CD8 记忆 T 细胞上 CD127 的表达模式。
方法/结果:选择 20 例 HBeAg 阳性的 CHB 患者,每天给予替比夫定 600mg 治疗 48 周。通过 CD45RA 和 CD27 标志物来鉴定记忆性 CD8 T 细胞。采用四色流式细胞术检测 CD8 T 细胞表面 CD127 的表达。结果显示,CHB 患者的记忆性 CD8 T 细胞上 CD127 的表达减少。CHB 患者血清 HBV DNA 和 HBeAg 水平与记忆性 CD8 T 细胞上 CD127 的表达呈强烈负相关。此外,成功的抗病毒治疗增加了 CHB 患者中 CD8 记忆 T 细胞以及 HBV 特异性 CD8 T 细胞上 CD127 的表达。
这些结果表明,CHB 患者中 CD8 记忆 T 细胞上 CD127 的表达减少是解释 CHB 感染中细胞免疫功能受损的潜在机制,而 CD8 记忆 T 细胞上 CD127 的表达是评估抗 HBV 治疗效果的有用指标。