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Relationship of human leukocyte antigen class II genes with the susceptibility to hepatitis B virus infection and the response to interferon in HBV-infected patients

机译:人类白细胞抗原II类基因与HBV感染患者对乙型肝炎病毒感染的敏感性及对干扰素的反应之间的关系

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摘要

AIM: To study the relationship of human leukocyte antigen (HLA)-DRB1 and -DQB1 alleles with the genetic susceptibility to HBV infection and the response to interferon (IFN) in HBV-infected patients.METHODS: Low-resolution DNA typing kit was used to determine HLA-DR-1 and -DQB1 genes in 72 patients with chronic hepatitis B (CHB) and HLA-DRB1 in 200 healthy people ready to donate their bone marrow in Shanghai. Among CHB patients, 35 were treated with IFNα -1b for 24 wk.RESULTS: The frequencies of HLA-DRB1*06, DRB1*08 and DRB1*16 alleles in 72 patients were higher than in 200 healthy people (2.08% vs 0%, OR = 3.837, P = 0.018; 11.11% vs 5.50%, OR = 2.148, P = 0.034; and 6.94% vs 3.00%, OR = 0.625, P = 0.049, respectively); whereas that of DRB1*07 allele was lower (2.78% vs 7.75%, OR = 0.340, P = 0.046). The frequency of HLA-DRB1* 14 allele was higher in 11 responders to IFN compared with 24 non-responders (18.18% vs 2.08%, OR = 10.444, P = 0.031), whereas that of DQB1*07 allele was inverse (9.09% vs 37.50%, OR = 0.167, P = 0.021).CONCLUSION: The polymorphism of HLA class II may influence the susceptibility to HBV infection and the response to IFN in studied CHB patients. Compared with other HLA-DRB1 alleles, HLA-DRB1*06, DRB1*08, and DRB1*16 may be associated with chronicity of HBV infection, HLA-DRB1*07 with protection against HBV infection, and HLA-DRB1*14 allele may be associated with a high rate of the response of CHB patients to IFN treatment. Compared with other HLA-DQB1 alleles, HLA-DQB1*07 may be associated with low response rate to IFN.
机译:目的:研究人白细胞抗原(HLA)-DRB1和-DQB1等位基因与HBV感染患者对HBV感染的遗传易感性和对干扰素(IFN)的反应之间的关系。方法:使用低分辨率DNA分型试剂盒在上海的200名准备捐献骨髓的健康人群中,确定72例慢性乙型肝炎(CHB)和HLA-DRB1患者的HLA-DR-1和-DQB1基因。在CHB患者中,有35例接受IFNα-1b治疗24周。结果:72例患者中HLA-DRB1 * 06,DRB1 * 08和DRB1 * 16等位基因的频率高于200名健康人群(2.08%vs 0% ,OR = 3.837,P = 0.018; 11.11%vs 5.50%,OR = 2.148,P = 0.034; 6.94%vs 3.00%,OR = 0.625,P = 0.049);而DRB1 * 07等位基因则较低(2.78%对7.75%,OR = 0.340,P = 0.046)。 HLA-DRB1 * 14等位基因的频率在24位无反应者中比IFN更高(11.18%vs 2.08%,OR = 10.444,P = 0.031),而DQB1 * 07等位基因的频率则相反(9.09%) vs. 37.50%,OR = 0.167,P = 0.021)。结论:HLA II类的多态性可能影响研究的CHB患者对HBV感染的敏感性和对IFN的反应。与其他HLA-DRB1等位基因相比,HLA-DRB1 * 06,DRB1 * 08和DRB1 * 16可能与HBV感染的慢性相关,HLA-DRB1 * 07与HBV感染的保护有关,HLA-DRB1 * 14等位基因可能与CHB患者对IFN治疗的高反应率相关。与其他HLA-DQB1等位基因相比,HLA-DQB1 * 07可能与对IFN的低应答率相关。

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