Dietz Julia, Susser Simone, Berkowski Caterina, Perner Dany, Zeuzem Stefan, Sarrazin Christoph
Medical Department 1, Goethe University Hospital, Frankfurt, Germany.
PLoS One. 2015 Aug 28;10(8):e0134395. doi: 10.1371/journal.pone.0134395. eCollection 2015.
Different highly effective interferon-free treatment options for chronic hepatitis C virus (HCV) infection are currently available. Pre-existence of resistance associated variants (RAVs) to direct antiviral agents (DAAs) reduces sustained virologic response (SVR) rates by 3-53% in hepatitis C virus (HCV) genotype 1 infected patients depending on different predictors and the DAA regimen used. Frequencies of single and combined resistance to NS3, NS5A and NS5B inhibitors and consequences for the applicability of different treatment regimens are unknown. Parallel population based sequencing of HCV NS3, NS5A and NS5B genes in 312 treatment-naïve Caucasian HCV genotype 1 infected patients showed the presence of major resistant variants in 20.5% (NS3), 11.9% (NS5A), and 22.1% (NS5B) with important differences for HCV subtypes. In NS3, Q80K was observed in 34.7% and 2.1% of subtype 1a and 1b patients, respectively while other RAVs to second generation protease inhibitors were detected rarely (1.4%). Within NS5A RAVs were observed in 7.1% of subtype 1a and 17.6% in subtype 1b infected patients. RAVs to non-nucleoside NS5B inhibitors were observed in 3.5% and 44.4% of subtype 1a and 1b patients, respectively. Considering all three DAA targets all subtype 1a and 98.6% of subtype 1b infected patients were wildtype for at least one interferon free DAA regimen currently available. In conclusion, baseline resistance testing allows the selection of at least one RAVs-free treatment option for nearly all patients enabling a potentially cost- and efficacy-optimized treatment of chronic hepatitis C.
目前有多种针对慢性丙型肝炎病毒(HCV)感染的高效无干扰素治疗方案。对于丙型肝炎病毒(HCV)基因型1感染的患者,预先存在对直接抗病毒药物(DAA)的耐药相关变异(RAV)会使持续病毒学应答(SVR)率降低3%至53%,具体降低幅度取决于不同的预测因素和所使用的DAA方案。对NS3、NS5A和NS5B抑制剂的单药及联合耐药频率以及不同治疗方案的适用性后果尚不清楚。对312例未经治疗的白种人HCV基因型1感染患者的HCV NS3、NS5A和NS5B基因进行基于人群的平行测序,结果显示主要耐药变异的存在率分别为20.5%(NS3)、11.9%(NS5A)和22.1%,不同HCV亚型之间存在重要差异。在NS3中,Q80K分别在34.7%的1a亚型和2.1%的1b亚型患者中被观察到,而对第二代蛋白酶抑制剂的其他RAV很少被检测到(1.4%)。在NS5A中,1a亚型感染患者中有7.1%观察到RAV,1b亚型感染患者中有17.6%观察到RAV。对非核苷类NS5B抑制剂的RAV分别在3.5%的1a亚型和44.4%的1b亚型患者中被观察到。考虑到所有三个DAA靶点,所有1a亚型和98.6%的1b亚型感染患者对于目前可用的至少一种无干扰素DAA方案为野生型。总之,基线耐药性检测可为几乎所有患者选择至少一种无RAV的治疗方案,从而实现慢性丙型肝炎潜在的成本和疗效优化治疗。