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首页> 外文期刊>Current Respiratory Medicine Reviews >Human Leukocyte Antigens Class I and Class II: Associations and Distribution in Different Ethnic Groups of Patients with Pulmonary Tuberculosis
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Human Leukocyte Antigens Class I and Class II: Associations and Distribution in Different Ethnic Groups of Patients with Pulmonary Tuberculosis

机译:人类白细胞抗原I类和II类:肺结核患者不同种族的关联和分布

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摘要

Mycobacterium tuberculosis, the causative agent of pulmonary tuberculosis (TB), remains a major public health risk worldwide. It is still not clear why a small percentage of the infected progress to active disease during their lifetime. It seems likely that TB develops by complex environmental factors and genetic susceptibility. Genetic factors, such as Human Leukocyte Antigens (HLA) in particular, are important determinants of susceptibility to TB. The HLA system is a T cell restriction element closely related to immuneresponsive and immune-suppressive genes. The expression of particular HLA class I and II antigens in an individual determines the ability of that individual to respond to particular mycobacterial antigens and epitopes. The most frequently reported immunogenetic associations have been found with HLA-B5,-B8,-B15,- B27,-B35,-Cw5 antigens and DRB1*1501, DRB1*1506, DRB1*1601, DRB1*1602, DQB1*0501, DQB1*0502, DQB1*0503, DQB1*0601 alleles, but these associations varied in reported studies of TB patients from different races and ethnic populations from Asia, North and Latin America and Europe. Although variations were apparent in the antigens/alleles associated with susceptibility, the increase in the frequency of DR2 antigen and DQB*05 allele was remarkably consistent in the analysed populations. A negative correlation of M. tuberculosis with HLA-DR4,-DR6,-DR8 antigens, DRB1*07, DRB1*13 and DQB1*0201, DQB1*0301, DQB1*0402 alleles was noted, but reductions in the frequency of alleles associated with protection were inconsistent in TB patients from different ethnic groups.
机译:结核分枝杆菌是肺结核(TB)的病原体,仍然是全球范围内的主要公共卫生风险。尚不清楚为什么一小部分感染者在其一生中会发展为活动性疾病。结核病似乎是由复杂的环境因素和遗传易感性引起的。遗传因素,特别是人类白细胞抗原(HLA),是结核病易感性的重要决定因素。 HLA系统是与免疫应答和免疫抑制基因密切相关的T细胞限制元件。个体中特定HLA I类和II类HLA抗原的表达决定了该个体对特定分枝杆菌抗原和表位作出反应的能力。已发现与HLA-B5,-B8,-B15,-B27,-B35,-Cw5抗原和DRB1 * 1501,DRB1 * 1506,DRB1 * 1601,DRB1 * 1602,DQB1 * 0501, DQB1 * 0502,DQB1 * 0503,DQB1 * 0601等位基因,但是这些关联在来自亚洲,北美和拉丁美洲以及欧洲的不同种族和族群的结核病患者的报道研究中有所不同。尽管与易感性相关的抗原/等位基因存在明显差异,但在分析的人群中,DR2抗原和DQB * 05等位基因的频率显着增加。结核分枝杆菌与HLA-DR4,-DR6,-DR8抗原,DRB1 * 07,DRB1 * 13和DQB1 * 0201,DQB1 * 0301,DQB1 * 0402等位基因呈负相关,但等位基因相关频率降低来自不同种族的结核病患者在保护方面并不一致。

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