Alphabio Laboratory, Ambroise Paré Hospital, Marseille, France.
J Med Virol. 2010 Dec;82(12):2027-31. doi: 10.1002/jmv.21909.
A lack of antiviral response in patients with chronic hepatitis C treated with pegylated (PEG)-interferon (IFN)-α-2a + ribavirin (RIBA) may be explained by neutralizing antibodies to IFN-α-2a. The aim of this study was to assess neutralizing antibodies to IFN-α-2a and IFN levels in non-responder patients who were re-treated by PEG IFN-α-2a and RIBA for 12 weeks. Non-responders to a first-line treatment of PEG IFN-α-2a + RIBA were included for treatment with PEG IFN-α-2a (180 µg/week) + RIBA (1,000 mg/day if <75 kg, 1,200 mg otherwise) for 48 weeks. HCV RNA was measured at week 12. IFN levels and neutralizing antibodies to IFN-α-2a were measured retrospectively on stored sera at baseline and weeks 4 and 12, using a quantitative sandwich ELISA for neutralizing antibodies to IFN-α-2a. Twenty-three patients were non-responders and 19 patients were responders at week 12 of the initial phase of the second-line treatment. Non-responders and responders did not differ statistically: baseline age (median age 47 vs. 50 years), HCV RNA (median 6.8 vs. 6.4 log(10) copies/ml), gender (70% vs. 73% males), genotype (genotype 1: 91% vs. 80%). The median IFN-α-2a levels (pg/ml) at weeks 0, 4, and 12 (interquartile range) did not differ between the 19 responders to initial phase of second-line treatment and the 23 non-responders: <3.3 (<3.3-371.4), 1457.3 (106.8-3284.8), and 1,652 (90.8-5,000); 84.5 (3.3-277.4), 1407.4 (120.2-2443.4), and 1620.1 (120.2-2287.1), respectively. Among non-selected consecutive non-responder patients, re-treatment with PEG IFN-α-2a + RIBA is associated with virological response regardless of the presence of antibody-mediated resistance to conventional IFN treatment.
在接受聚乙二醇(PEG)-干扰素(IFN)-α-2a+利巴韦林(RIBA)治疗的慢性丙型肝炎患者中,抗病毒反应缺乏可能归因于对 IFN-α-2a 的中和抗体。本研究的目的是评估在接受 PEG IFN-α-2a+RIBA 治疗 12 周后再次治疗的无应答患者的 IFN-α-2a 中和抗体和 IFN 水平。首先,将一线治疗 PEG IFN-α-2a+RIBA 无应答的患者纳入治疗,给予 PEG IFN-α-2a(180μg/周)+RIBA(75kg 以下为 1000mg/天,否则为 1200mg/天)治疗 48 周。在二线治疗的初始阶段第 12 周时测量 HCV RNA。使用针对 IFN-α-2a 的定量夹心 ELISA 检测,在基线和第 4 周和第 12 周时对储存的血清进行 IFN 水平和 IFN-α-2a 中和抗体的回顾性检测。有 23 名患者为无应答者,19 名患者为有应答者。无应答者和有应答者在统计学上无差异:基线年龄(中位年龄 47 岁与 50 岁)、HCV RNA(中位值 6.8 与 6.4 log(10) 拷贝/ml)、性别(70%与 73%为男性)、基因型(基因型 1:91%与 80%)。在第 19 名对二线治疗初始阶段有反应的患者和第 23 名无反应的患者中,在第 0、4 和 12 周(四分位间距)的 IFN-α-2a 水平(pg/ml)中位数没有差异:<3.3(<3.3-371.4)、1457.3(106.8-3284.8)和 1652(90.8-5000);84.5(3.3-277.4)、1407.4(120.2-2443.4)和 1620.1(120.2-2287.1)。在未选择的连续无应答患者中,PEG IFN-α-2a+RIBA 的重新治疗与病毒学应答相关,而与对常规 IFN 治疗的抗体介导耐药性无关。