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Rapid decrease in titer and breadth of neutralizing anti-HCV antibodies in HIV/HCV-coinfected patients who achieved SVR

机译:在获得SVR的HIV / HCV合并感染患者中中和抗HCV抗体的效价和广度迅速降低

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摘要

The main targets for neutralizing anti-hepatitis C virus (HCV) antibodies (HCV-nAbs) are the E1 and E2 envelope glycoproteins. We have studied the characteristics of HCV-nAbs through a retrospective study involving 29 HIV/HCV-coinfected patients who achieved sustained virological response (SVR) with peg-IFNα + ribavirin anti-HCV therapy. Plasma samples at baseline and week 24 after SVR were used to perform neutralization assays against five JFH1-based HCV recombinant viruses coding for E1 and E2 from genotypes 1a (H77), 1b (J4), 2a (JFH1), 3a (S52) and 4a (ED43). At baseline, the majority of plasma samples neutralized 1a, 1b, 2a, and 4a, but not 3a, genotypes. Twenty-four weeks following SVR, most neutralizing titers declined substantially. Furthermore, titers against 3a and 2a were not detected in many patients. Plasma samples with high HCV-nAb titers neutralized all genotypes, and the highest titers at the starting point correlated with the highest titers at week 24 after SVR. In conclusion, high titers of broad-spectrum HCV-nAbs were detected in HIV/HCV-coinfected individuals, however, those titers declined soon after SVR.
机译:中和抗丙型肝炎病毒(HCV)抗体(HCV-nAbs)的主要目标是E1和E2包膜糖蛋白。我们通过一项回顾性研究研究了HCV-nAbs的特征,该研究涉及29名接受peg-IFNα+ ribavirin抗HCV治疗的HIV / HCV合并感染患者,实现了持续的病毒学应答(SVR)。 SVR后基线和第24周时的血浆样本用于对五种基于JFH1的HCV重组病毒进行中和分析,这些病毒编码基因型1a(H77),1b(J4),2a(JFH1),3a(S52)和E1和E2 4a(ED43)。在基线时,大多数血浆样品中和了1a,1b,2a和4a基因型,但未中和3a基因型。 SVR后二十四周,大多数中和效价大幅下降。此外,在许多患者中未检测到针对3a和2a的效价。具有高HCV-nAb滴度的血浆样品中和了所有基因型,在SVR后第24周,起始点的最高滴度与最高滴度相关。总之,在感染了HIV / HCV的个体中检测到高滴度的广谱HCV-nAb,但是,这些滴度在SVR之后不久就下降了。

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