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慢性乙型肝炎患者HBV前C区及BCP区变异与血清细胞因子的关系 被引量:2

The relationship between HBV precore and basal core promoter mutations and serum cytokines in patients with chronic hepatitis B
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摘要 目的探讨乙型肝炎e抗原(HBeAg)阴性和阳性慢性乙型肝炎(CHB)患者乙型肝炎病毒(HBV)前C区、基本核心启动子(BCP)区变异特点以及与血清细胞因子干扰素(IFN)-γ、白细胞介素(IL)-10水平的关系。方法将120例HBV DNA阳性CHB患者(HBeAg阴性和阳性各60例)与60例健康体检者(对照组)纳入研究。荧光定量聚合酶链反应(PCR)法检测HBeAg阴性和阳性组患者HBV DNA水平,直接测序法检测两组前C区G1896A变异及BCP区A1762T和G1764A变异,双抗夹心酶联免疫吸附试验检测血清细胞因子IFN-γ/、IL-10的水平。结果 120例HBV DNA阳性CHB患者HBV前C区和BCP区变异总检出率为60.00%(72/120),其中HBeAg阴性组变异检出率为80.00%(48/60),HBeAg阳性组变异检出率为40.00%(24/60),两组比较,差异有显著性(x^2=20.00,P=0.000)。HBeAg阴性组G1896A变异(38.33%)和联合变异(G1896A、A1762T和G1764A同时变异,25.00%)的检出率明显高于HBeAg阳性组(16.67%、0.00%)(分别x^2=7.06,P=0.008;x^2=17.14,P=0.000)。变异组血清IFN-7水平为(102.33±27.20)pg/mL,明显高于无变异组(79.18±16.43)pg/mL及对照组(35.77±4.23)pg/mL(分别t=5.72,t=19.33,均P=0.000);变异组血清IL-10水平为(28.13±7.00)pg/mL,明显高于无变异组(13.91±5.42)pg/mL及对照组(13.68±2.27)pg/mL(分别t=12.50,t=15.65,均P=0.000)。结论 G1896A变异和联合变异更常见于HBeAg阴性CHB;G1896A和A1762T/G1764A变异与血清细胞因子IFN-γ和IL-10水平升高有关。 Objective To study the characteristics of hepatitis B virus (HBV) preeore G1896A mutation and basal core promoter (BCP) A1762T and G1764A mutations among HBeAg-negative and HBeAg-positive chronic hepatitis B (CHB) patients, and to explore the relationship between the above mutations and the serum levels of interferon-7 (IFN-γ) and interleukin-10 (IL-10) in these patients. Methods 120 patients with HBV DNA positive CHB including 60 HBeAg-negative CHB (group A) and 60 HBeAg-positive CHB (group B), and 60 healthy persons were enrolled in this study. The serum HBV DNA of group A and B were determined by real-time fluorescence quantitative polymerase chain reaction (PCR). The HBV precore G1896A mutation and BCP A1762T and G1764A mutation in group A and B were detected by PCR and direct sequencing. The levels of IFN-γ and IL-10 in serum were measured by enzyme linked immunosorbent assay. Results The total incidence of preeore and BCP mutations was 60. 00% (72/120) in 120 patients, the incidence of precore and BCP mutation in group A and B was 80. 00% (48/60) and 40. 00% (24/60) respectively (x^2 = 20. 00,P = 0. 000). The incidence of precore G1896A mutation (38. 33%) and the united mutation (G1896A and A1762T and G1764A mutation, 25.00%) in group A were significantly higher than those in group B (16. 67 %, 0. 00 %) (x^2 = 7. 06, P = 0. 008; x^2 = 17. 14, P = 0. 000). The serum level of IFN-γ in the mutation group were(102. 33 ± 27. 20)pg/mL, which were significantly higher than (79. 18 ± 16. 43)pg/mL in the non-mutation group (t = 5.72,P = 0. 000) and (35.77 ± 4. 23)pg/mL in the healthy control group (t = 19. 33,P = 0. 000) . The serum level of IL-10 in the mutation group were(28. 13 ± 7. 00)pg/mL , which were also significant ly higher than( 13.91 ± 5.42)pg/mL in the non-mutation group(t = 12. 50, P = 0. 000) and (13.68 ± 2. 27)pg/mL in the healthy control group (t = 15.65,P = 0. 000). Conclusion The G1896A mutation and the united mutation commonly occur in the HBeAg negative CHB patients. The mutations of G1896A and A1762T/G1764A may be related to the serum increased levels of IFN- γ and IL-10.
出处 《中国感染控制杂志》 CAS 2010年第5期320-323,共4页 Chinese Journal of Infection Control
关键词 肝炎 乙型 慢性 肝炎病毒 乙型 前核心区 基本核心启动子 基因变异 干扰素-Γ 白细胞介素-10 hepatitis B, chronic hepatitis B virus preeore basal core promoter gene mutation interferon-γ interleukin-10
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