Beijing You'an Hospital, Capital Medical University, Beijing, China.
Liver Int. 2012 Jan;32(1):102-9. doi: 10.1111/j.1478-3231.2011.02652.x. Epub 2011 Sep 26.
Virus-specific T-cell responses play a major role in antiviral immune response. However, the effect of hepatitis C virus (HCV)-specific T-cell responses on combination therapy still remains controversial.
To identify the association between HCV-specific T cell responses and efficiency of combination therapy.
To address this issue, a longitudinal analysis of HCV-specific T-cell responses to overlapping peptides covering HCV-nonstructural protein (NS) was performed using ELISpot assay in 48 chronically infected HCV-1b patients during combination treatment with peginterferon-alfa and ribavirin.
Fifty-two percent of chronic HCV patients showed detectable HCV-NS3, NS4 or NS5A specific T-cell responses before therapy, with NS3 appearing to be the most immunodominant protein followed by NS5A and NS4. In addition, the percentage of patients responding to peptide stimulation was higher in patients with sustained virological response (SVR) when compared with those without SVR. Dynamics of HCV-NS-specific T-cell responses were further analysed; we found that HCV-specific T-cell responses maintained higher levels at 12 weeks into treatment in patients with SVR. In contrast, HCV-specific T-cell responses in patients without SVR declined significantly at 4 weeks into treatment and maintained low levels at 12 weeks.
We found that the HCV-specific T-cell responses were associated with good viral control in patients with combination therapy.
病毒特异性 T 细胞应答在抗病毒免疫反应中起着重要作用。然而,丙型肝炎病毒(HCV)特异性 T 细胞应答对联合治疗的影响仍存在争议。
确定 HCV 特异性 T 细胞应答与联合治疗效果之间的关系。
为解决这个问题,我们使用 ELISpot 测定法对 48 例慢性 HCV-1b 感染患者在聚乙二醇干扰素-α和利巴韦林联合治疗期间对重叠肽的 HCV-非结构蛋白(NS)进行了 HCV 特异性 T 细胞应答的纵向分析。
52%的慢性 HCV 患者在治疗前可检测到 HCV-NS3、NS4 或 NS5A 特异性 T 细胞应答,其中 NS3 似乎是最免疫优势的蛋白,其次是 NS5A 和 NS4。此外,与无 SVR 患者相比,对肽刺激有反应的患者在 SVR 患者中比例更高。进一步分析 HCV-NS 特异性 T 细胞应答的动力学;我们发现,在 SVR 患者中,治疗 12 周时 HCV 特异性 T 细胞应答保持较高水平。相比之下,无 SVR 患者的 HCV 特异性 T 细胞应答在治疗 4 周时显著下降,并在 12 周时保持低水平。
我们发现,HCV 特异性 T 细胞应答与联合治疗患者的良好病毒控制有关。