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HCV-specific CD8+ cell detection at week 12 of chronic hepatitis C treatment with PEG-interferon-α2b/ribavirin correlates with infection resolution

机译:在PEG-干扰素-α2b/利巴韦林治疗慢性丙型肝炎的第12周时,HCV特异性CD8 +细胞的检测与感染的缓解相关

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Lower than 2-log viral-load (VL) decrease at week 12 (w12) of chronic hepatitis C (CHC) treatment with Peg-interferon/ribavirin has 100% negative predictive value (PV) of sustained virologic response (SVR), and this could be related with absence of HCV-specific cytotoxic T lymphocyte (CTL) response. In this study, percentage of cases with SVR, according to peripheral HCV-specific cytotoxic response at w12, was analysed (Group-1: detection+, Group-2: detection-). SVR was higher in group-1 (93%) than in group-2 (47%) (p=0.003). An increase on HCV-specific CTL frequency between baseline and w12 and higher specific reactivity were observed in group-1 (p=0.011 and p=0.025). HCV-specific CTL detection at w12 correlated with level of VL decrease (p=0.016, r=0.389), and among HCV genotype-1 patients with either early or delayed virologic response (EDVR), 100% positive PV of SVR was observed. In summary, HCV-specific CTL detection at w12 of Peg-interferon/ribavirin treatment correlates with SVR and in EDVR genotype-1 cases predicts SVR.
机译:在接受聚乙二醇干扰素/利巴韦林治疗的慢性丙型肝炎(CHC)的第12周(w12),病毒载量(VL)下降低于2对数,并具有持续病毒学应答(SVR)的100%阴性预测值(PV),并且这可能与缺乏HCV特异性细胞毒性T淋巴细胞(CTL)反应有关。在这项研究中,根据第12周时外周HCV特异性细胞毒性反应,分析了SVR病例的百分比(第1组:检测+,第2组:检测-)。第1组的SVR(93%)高于第2组的(47%)(p = 0.003)。在第1组中观察到HCV特异性CTL频率在基线和w12之间增加,并且比反应活性更高(p = 0.011和p = 0.025)。在第12周时,HCV特异性CTL检测与VL降低水平相关(p = 0.016,r = 0.389),在早期或延迟病毒学应答(EDVR)的HCV基因型1患者中,观察到100%的SVR阳性PV。总之,聚乙二醇干扰素/利巴韦林治疗第12周时HCV特异性CTL检测与SVR相关,在EDVR基因型为1的病例中可预测SVR。

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