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Diversity and frequencies of HLA class I and class II genes of an East African population

机译:东非人口的HLA I类和II类基因的多样性和频率

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摘要

Human Leukocyte Antigens (HLAs) play an important role in host immune responses to infectious pathogens, and influence organ transplantation, cancer and autoimmune diseases. In this study we conducted a high resolution, sequence-based genotyping of HLA class I and class II genes of more than 2000 women from Kenya, eastern Tanzania and southern Uganda around Lake Victoria and analyzed their allele, phenotype and haplotype frequencies. A considerable genetic diversity was observed at both class I and II loci. A total of 79 HLA-A, 113 HLA-B, 53 HLA-C, 25 HLA-DPA1, 60 HLA-DPB1, 15 HLA-DQA1, 44 HLA-DQB1 and 38 HLA-DRB1 alleles have been identified. The most common class I alleles were A * 02:01:01 (10.90%), B * 58:02 (8.79%), and C * 06:02:01 (16.98%). The most common class II alleles were DPA1*01:03:01 (40.60%), DPB1 * 01:01:01 (23.45%), DQA1 * 01:02:01 (31.03%), DQB1 * 03:01:01 (21.79%), DRB1 * 11:01:02 (11.65%), DRB3 * 02:02:01 (31.65%), DRB4 * 01:01:01 (10.50%), and DRB5 * 01:01:01 (10.50%). Higher than expected homozygosity was observed at HLA-B (P = 0.022), DQA1 (P = 0.004), DQB1 (P = 0.023), and DRB1 (P = 0.0006) loci. The allele frequency distribution of this population is very similar to the ones observed in other sub-Saharan populations with the exception of lower frequencies of A * 23 (5.55% versus 11.21%) and DQA1 * 03 (4.79% versus 11.72%), and higher frequencies of DPB1 * 30 (2.26% versus 0.37%) and DRB1 * 11 (21.51% versus 15.89%). The knowledge of the diversity and allele/ phenotype frequencies of the HLA alleles of this east African population, can contribute to the understanding of how host genetic factors influence disease susceptibility and effective anti-retroviral treatment of HIV infections and future vaccine trials.
机译:人类白细胞抗原(HLA)在宿主对传染性病原体的免疫反应中起重要作用,并影响器官移植,癌症和自身免疫性疾病。在这项研究中,我们对维多利亚湖周围肯尼亚,坦桑尼亚东部和乌干达南部的2000多名妇女的HLA I类和II类基因进行了基于序列的高分辨率基因分型,并分析了其等位基因,表型和单倍型频率。在I类和II类基因座上均观察到相当大的遗传多样性。总共鉴定出79个HLA-A,113个HLA-B,53个HLA-C,25个HLA-DPA1、60个HLA-DPB1、15个HLA-DQA1、44个HLA-DQB1和38个HLA-DRB1等位基因。 I类最常见的等位基因是A * 02:01:01(10.90%),B * 58:02(8.79%)和C * 06:02:01(16.98%)。最常见的II类等位基因是DPA1 * 01:03:01(40.60%),DPB1 * 01:01:01(23.45%),DQA1 * 01:02:01(31.03%),DQB1 * 03:01:01 (21.79%),DRB1 * 11:01:02(11.65%),DRB3 * 02:02:01(31.65%),DRB4 * 01:01:01(10.50%)和DRB5 * 01:01:01( 10.50%)。在HLA-B(P = 0.022),DQA1(P = 0.004),DQB1(P = 0.023)和DRB1(P = 0.0006)位点观察到高于预期的纯合性。该人群的等位基因频率分布与其他撒哈拉以南人群的频率分布非常相似,除了较低的A * 23(5.55%对11.21%)和DQA1 * 03(4.79%对11.72%)的频率,以及DPB1 * 30(2.26%对0.37%)和DRB1 * 11(21.51%对15.89%)的较高频率。对这一东非人口的HLA等位基因的多样性和等位基因/表型频率的了解,可以有助于了解宿主遗传因素如何影响疾病的易感性以及对HIV感染的有效抗逆转录病毒治疗以及未来的疫苗试验。

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