摘要
目的探讨人类白细胞抗原(HLA)DQAI基因多态性与乙型肝炎病毒(HBV)感染临床结局的关联。方法临床收集慢性乙型肝炎(120例)、慢性HBV携带者(60例)、自限性HBV感染者(60例)三组病例,前两组诊断均经肝活检证实。聚合酶链反应序列特异性引物(PCR-SSP)法检测HIA-DQA1基因型,比较组间基因频率的差异。结果(1)HLA-DQA1*0201在慢性乙型肝炎组的分布频率显著高于自限性HBV感染组(38.3% vs 5.8%,P〈0.001,A=10.04,95% CI:4.48—22.48);HLA-DQA1*0102的分布频率显著低于自限性HBV感染组(9.6% vs 36.7%,P〈0.001,A=0.183,95% CI:0.10—0.32)。(2)HLA-DQA1*0201在慢性乙型肝炎组的分布频率显著高于慢性HBV携带者组(38.3%vs 7.5%,P〈0.01,A=7.667,95% CI:3.7—15.87);HLA-DQA1*0102的分布频率显著低于慢性HBV携带者(20%vs 9.6%,P〈0.01,A=0.424,95%CI:0.23—0.79)。结论HLA-DQA1基因多态性影响HBV感染临床结局,其中DQA1*0102呈保护作用,DQA1*0201可能促进HBV感染的慢性化和肝炎的发生。
Objective To investigate the association between HLA-DQA1 gene polymorphism and the outcomes of hepatitis B virus infection in Chinese Han population. Methods A total of 180 consecutive patients with biopsy-proven hepatitis B virus infection (120 patients with chronic hepatitis B and 60 patients with asymptomatic HBV carrier) and 60 subjects who resolved from HBV infection spontaneously were studied. Genotype of human leukocyte antigen( HLA)-DQA1 was detected by polymerase chain reaction sequence specific primer(PCR-SSP).Results(1)The frequency of HLA-DQA1*0201 allele in chronic hepatitis B group was significant higher than the frequency in resolved from HBV infection spontaneously group(38.3 % vs 5.8 %, P 〈 0.001, A = 10.04, 95% CI: 4.48-22.48) . The frequency of HLA-DQA1*0102 allele in chronic hepatitis B group was significant lower than the frequency in resolved from HBV infection spontaneously group (9.6% vs 36.7% ,P 〈 0.001, A = 0.183, 95% CI:0.10-0.32). (2) The frequency of HLA-DQA1*0201 allele in chronic hepatitis B group was significant higher than the frequency in asymptomatic HBV carrier group(38.3 % vs 7.5%, P 〈 0.01, A = 7.667,95% CI:3.7-15.87). The frequency of HLA-DQA1 *0102 allele in chronic hepatitis B group was significant lower than the frequency in asymptomatic HBV carrier group(20% vs 9.6%, P 〈 0.O1,A = 0.424,95% CI:0.23-0.79). Conclusion HLA-DQA1 gene polymorphism may play an important role in the outcomes of hepatitis B virus infection in Chinese Han population. The HLA-DQA1*0102 allele could keep individuals away from HBV infection, and HLA-DQA1*0201 allele could aggravate persistant infection of HBV and hepatic inflammatory.
出处
《中华实验和临床病毒学杂志》
CAS
CSCD
北大核心
2009年第6期430-433,共4页
Chinese Journal of Experimental and Clinical Virology
基金
浙江省中医药科技计划项目(2007CB199).