HLAⅱ类位点的研究表明DQB1*03:03:02是巴基斯坦人群哮喘的危险因素

IF 2.3 4区 医学 Q3 GENETICS & HEREDITY International Journal of Immunogenetics Pub Date : 2022-10-22 DOI:10.1111/iji.12602
Nusrat Saba, Ghazala Kaukab Raja, Osman Yusuf, Sadia Rehman, Saeeda Munir, Sumaira Sajjad, Atika Mansoor
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引用次数: 0

摘要

哮喘是肺部和呼吸道的一种慢性炎症性疾病,通常是多种环境和遗传因素共同作用的结果。6p21染色体上的人类白细胞抗原(HLA)区域编码人类基因组中多态性最高的位点,编码在免疫功能中起核心作用的基因,其中HLA位点与各种免疫介导的疾病(如自身免疫、过敏和感染)密切相关。HLAⅱ类基因DRB1和DQB1等等位基因是哮喘发生的关键遗传标记,在世界不同种族人群中被广泛研究。然而,巴基斯坦哮喘患者HLAⅱ类等位基因和单倍型的遗传筛选尚未见报道。本研究的目的是在巴基斯坦人群中筛选哮喘病例和对照人群中的HLAⅱ类DRB1和DQB1等位基因。采用序列特异性聚合酶链反应法对702例健康对照和哮喘患者进行HLAⅱ型基因分型。计算HLA-DRB1和HLA-DQB1等位基因和单倍型频率,并确定其与哮喘的风险或保护性关联。采用Arlequin 3.1版软件进行DRB1和DQB1等位基因双位点单倍型的代入。与DRB1相比,与哮喘相关的信号在DQB1位点更强。HLA DQB1*03:03:02(优势比[OR] = 2.42, 95%可信区间[CI] = 1.34-4.25)与哮喘风险增加显著相关,单倍型包含等位基因DRB1*07:01-DQB1*03:03:02 (OR = 2.40, 95% CI = 1.25-4.62)。相比之下,DQB1*06 (OR = 0.39, 95% CI = 0.22-0.70)和DQB1*06:02 (OR = 0.27, 95% CI = 0.10-0.71)成为哮喘的保护等位基因。我们的数据表明,HLA DQB1*03:03:02等位基因是哮喘的危险等位基因,而两个DQB1等位基因DQB1*06和DQB1*06:02与哮喘保护相关。我们的研究结果强调了HLA-DQB1等位基因在巴基斯坦哮喘发病机制中的重要作用。需要更多的研究,特别是更大的研究队列来证实HLA DQB1*03:03:02作为预测标志物的效用。
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Study of HLA class II loci reveals DQB1*03:03:02 as a risk factor for asthma in a Pakistani population

Asthma, a chronic inflammatory disorder of the lungs and airways, typically results from a combination of multiple environmental and genetic factors. Human leucocyte antigen (HLA) region on chromosome 6p21 encodes the most highly polymorphic loci in the human genome, encoding genes with central roles in the immune function where HLA loci are strongly associated with various immune-mediated diseases such as autoimmunity, allergies and infection. The alleles of HLA class II genes such as DRB1 and DQB1 are the key genetic markers in the development of asthma and have been extensively studied in different ethnicities of the world population. However, the genetic screening of HLA class II alleles and haplotypes in Pakistani asthmatics has not been studied so far. The aim of the present study was to screen the HLA class II DRB1 and DQB1 alleles in asthma cases and controls in a Pakistani population. Seven hundred and two healthy controls and asthma patients were genotyped for HLA class II by sequence-specific polymerase chain reaction assays. The HLA-DRB1 and HLA-DQB1 allele and haplotype frequencies were calculated, and their risk or protective association with asthma was determined. Two-locus haplotypes of DRB1 and DQB1 alleles were imputed using Arlequin version 3.1 software. The signals of association with asthma were stronger at the DQB1 locus as compared to DRB1. HLA DQB1*03:03:02 (odds ratio [OR] = 2.42, 95% confidence interval [CI] = 1.34–4.25) was significantly associated with an increased risk of asthma, as was the haplotype comprised allele DRB1*07:01-DQB1*03:03:02 (OR = 2.40, 95% CI = 1.25–4.62). In contrast, DQB1*06 (OR = 0.39, 95% CI = 0.22–0.70) and DQB1*06:02 (OR = 0.27, 95% CI = 0.10–0.71) emerged as protective alleles for asthma. Our data concludes that the HLA DQB1*03:03:02 allele was a risk allele for asthma, whereas two DQB1 alleles, DQB1*06 and DQB1*06:02, were associated with asthma protection. Our findings highlight a prominent role for HLA-DQB1 alleles in asthma pathogenesis in studied Pakistani cases. More studies, especially with a larger study cohort are needed to confirm the utility of HLA DQB1*03:03:02 as a predictive marker.

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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are: -studies of blood groups and other surface antigens- cell interactions and immune response- receptors, antibodies, complement components and cytokines- polymorphism- evolution of the organisation, control and function of immune system components- anthropology and disease associations- the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies- All papers are seen by at least two independent referees and only papers of the highest quality are accepted.
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Does HLA-DQA1*05 carriage have a greater impact on the outcome of infliximab therapy for isolated small-bowel Crohn's disease? Investigations of associations between TNF-α promoter polymorphisms and genetic susceptibility to type 2 diabetes mellitus: A cross-sectional study in Chinese Han population. Issue Information Abstracts Author Index
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