Erhardt A, Reineke U, Blondin D, Gerlich W H, Adams O, Heintges T, Niederau C, Häussinger D
Department of Internal Medicine, Division of Gastroenterology, Hepatology, and Infectious Diseases, Heinrich-Heine-University of Düsseldorf, Düsseldorf, Germany.
Hepatology. 2000 Mar;31(3):716-25. doi: 10.1002/hep.510310323.
In chronic replicative hepatitis B the significance of mutations in the basic core promoter (BCP), core upstream regulatory sequences (CURS) and negative regulatory element (NRE) for response to interferon (IFN) is unknown. A sequence analysis of the NRE, CURS, BCP, and precore region was performed from sera of 96 patients with chronic replicative hepatitis B (64 hepatitis B e antigen [HBeAg]-positive patients and 32 HBeAg-negative patients) treated with alfa-IFN (IFN-alpha). The overall sustained response (SR) rate to IFN was 30% with no significant difference between HBeAg-positive and HBeAg-negative patients. IFN responsiveness correlated to hepatitis B virus (HBV)-DNA levels, hepatitis B surface antigen (HBsAg) levels, the number of mutations in the complete BCP, especially nucleotide (nt) region 1753 to 1766 and mutations at nt 1762 and 1764. In HBeAg-positive hepatitis, SR to IFN was associated with a high number of mutations in the BCP (P <.04) and nucleotide region 1753 to 1766 (P <.015) as well as mutations at nucleotide 1764 (P <.007). In HBeAg-negative hepatitis, SR to IFN correlated with a low number of mutations in the BCP (P <.04) and nucleotide region 1753 to 1766 (P <.02) and a wild-type sequence at nt 1764 (P <.003). Prediction of IFN response was possible on the basis of nt 1764 in 77% of HBeAg-positive patients and 78% of HBeAg-negative patients. IFN response did not correlate with the occurrence of the 1896 mutation, mutations in the CURS or NRE, disease duration, ethnic origin of the patient, alanine transaminase (ALT) levels and HBV genotype. Our data suggest that HBV genome mutations located within the BCP are determinants of a response to IFN therapy.
在慢性复制型乙型肝炎中,基本核心启动子(BCP)、核心上游调控序列(CURS)和负调控元件(NRE)中的突变对干扰素(IFN)治疗反应的意义尚不清楚。对96例接受α干扰素(IFN-α)治疗的慢性复制型乙型肝炎患者(64例乙型肝炎e抗原[HBeAg]阳性患者和32例HBeAg阴性患者)的血清进行了NRE、CURS、BCP和前核心区的序列分析。IFN的总体持续应答(SR)率为30%,HBeAg阳性和HBeAg阴性患者之间无显著差异。IFN反应性与乙型肝炎病毒(HBV)-DNA水平、乙型肝炎表面抗原(HBsAg)水平、完整BCP中的突变数量,特别是核苷酸(nt)区域1753至1766以及nt 1762和1764处的突变相关。在HBeAg阳性肝炎中,IFN的SR与BCP中大量突变(P <.04)、核苷酸区域1753至1766(P <.015)以及核苷酸1764处的突变(P <.007)相关。在HBeAg阴性肝炎中,IFN的SR与BCP中少量突变(P <.04)、核苷酸区域1753至1766(P <.02)以及nt 1764处的野生型序列(P <.003)相关。在77%的HBeAg阳性患者和78%的HBeAg阴性患者中,基于nt 1764可以预测IFN反应。IFN反应与1896突变的发生、CURS或NRE中的突变、病程、患者的种族、丙氨酸转氨酶(ALT)水平和HBV基因型无关。我们的数据表明,位于BCP内的HBV基因组突变是IFN治疗反应的决定因素。