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Association between HLA class II gene and susceptibility or resistance to chronic hepatitis B

机译:HLA II类基因与慢性乙型肝炎易感性或耐药性之间的关联

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AIM: To investigate the association between the polymorphism of HLA-DRB1, -DQA1 and -DQB1 alleles and viral hepatitis B. METHODS: HLA-DRB1, -DQA1 and -DQB1 alleles in 54 patients with chronic hepatitis B, 30 patients with acute hepatitis B and 106 normal control subjects were analyzed by using the polymerase chain reaction/sequence specific primer (PCR/SSP) technique. RESULTS: The allele frequency of HLA-DRB1~*0301 in the chronic hepatitis B group was markedly higher than that in the normal control group (17.31 % VS5.67 %), there was a significant correlation between them (x~2= 12.3068, PC=0.0074, RR=4.15). The allele frequency of HLA-DQA1~*0501 in the chronic hepatitis B group was significantly higher than that in the normal control group (25.96 % vs 13.68 %), there was a significant correlation between them (x~2=9.2002, PC=0.0157, RR=2.87). The allele frequency of HLA-DQB1~*0301 in the chronic hepatitis B group was notably higher than that in the normal control group (35.58 % vs 18.87 %), there was a significant correlation between them (x~2=15.5938, PC=0.0075, RR=4.07). The allele frequency of HLA-DRB1~*1101/1104 in the chronic hepatitis B group was obviously lower than that in the normal control group (0.96 % VS 13.33 %), there was a significant correlation between them (x~2=11.9206, PC=0.0145, RR=18.55). The allele frequency of HLA-DQA1~*0301 in the chronic hepatitis B group was remarkably lower than that in the normal control group (14.42 % VS 30 %), there was a significant correlation between them (x~2=8.7396, PC=0.0167, RR=0.35). CONCLUSION: HLA-DRB1*0301, HLA-DQA1~*0501 and HLA-DQB1~*0301 are closely related with susceptibility to chronic hepatitis B, and HLA-DRB1~*1101/1104 and HLA-DQA1~*0301 are closely related with resistance to chronic hepatitis B. These findings suggest that host HLA class II gene is an important factor determining the outcome of HBV infection.
机译:目的:探讨HLA-DRB1,-DQA1和-DQB1等位基因多态性与乙型病毒性肝炎的关系。方法:HLA-DRB1,-DQA1和-DQB1等位基因在54例慢性乙型肝炎,30例急性肝炎中通过使用聚合酶链反应/序列特异性引物(PCR / SSP)技术分析B和106名正常对照受试者。结果:慢性乙型肝炎患者HLA-DRB1〜* 0301等位基因频率明显高于正常对照组(17.31%VS5.67%),两者之间存在显着相关性(x〜2 = 12.3068) ,PC = 0.0074,RR = 4.15)。慢性乙型肝炎组HLA-DQA1〜* 0501等位基因频率显着高于正常对照组(25.96%vs 13.6%),两者之间存在显着相关性(x〜2 = 9.2002,PC = 0.0157,RR = 2.87)。慢性乙型肝炎患者HLA-DQB1〜* 0301的等位基因频率明显高于正常对照组(35.58%vs 18.87%),两者之间存在显着相关性(x〜2 = 15.5938,PC = 0.0075,RR = 4.07)。慢性乙型肝炎患者HLA-DRB1〜* 1101/1104等位基因频率明显低于正常对照组(0.96%VS 13.33%),两者之间存在显着相关性(x〜2 = 11.9206, PC = 0.0145,RR = 18.55)。慢性乙型肝炎患者HLA-DQA1〜* 0301的等位基因频率明显低于正常对照组(14.42%VS 30%),两者之间存在显着相关性(x〜2 = 8.7396,PC = 0.0167,RR = 0.35)。结论:HLA-DRB1 * 0301,HLA-DQA1〜* 0301和HLA-DQB1〜* 0301与慢性乙型肝炎的易感性密切相关,HLA-DRB1〜* 1101/1104和HLA-DQA1〜* 0301密切相关这些发现表明宿主HLA II类基因是决定HBV感染结果的重要因素。

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