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首页> 外文期刊>Human Immunology: Official Journal of the American Society for Histocompatibility and Immunogenetics >Immunogenetic factors in early immune control of human immunodeficiency virus type 1 (HIV-1) infection: Evaluation of HLA class I amino acid variants in two African populations
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Immunogenetic factors in early immune control of human immunodeficiency virus type 1 (HIV-1) infection: Evaluation of HLA class I amino acid variants in two African populations

机译:人免疫缺陷病毒早期免疫控制中的免疫发生因子(HIV-1)感染:两种非洲群体中HLA A类的氨基酸变种评价

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摘要

Immune control of HIV-1 infection depends heavily on cytotoxic T-lymphocyte responses restricted by diverse HLA class I molecules. Recent work has uncovered specific amino acid residues (AARs) that seem to dictate the extent of immune control in African Americans, which prompted us to test these emerging hypotheses in seroconverters (SCs) from southern and eastern Africa. Based on data from 196 Zambians and 76 Rwandans with fully resolved HLA alleles and pre-therapy HIV-1 viral loads (VL) in the first 3- to 36-month of infection (2300 person-visits), four AARs of primary interest (positions 63, 97, 116 and 245 in the mature HLA-B protein) were found to explain 8.1% and 15.8% of variance in set-point VL for these cohorts (P=.024 and 7.5 x 10(-6), respectively). Two AARs not reported previously (167S in HLA-B and 116F in HLA-C) also showed relatively consistent associations with VL (adjusted P=.009-.069), while many population-specific associations were also noted (false discovery rate 0.05). Extensive and often strong linkage disequilibrium among neighboring AAR variants called for more extensive analyses of AAR haplotypes in diverse cohorts before the structural basis of antigen presentation can be fully comprehended.
机译:HIV-1感染的免疫控制大量取决于细胞毒性T淋巴细胞反应,受到不同HLA I类分子的限制。最近的工作已经发现了似乎在非洲裔美国人的免疫控制范围内发现了特定的氨基酸残基(AARs),这促使我们在南部和东非的血管转换器(SCS)中测试这些新兴假设。基于196年的Zambians和76个rwandans的数据在感染的前3至36个月(& 2300人访问)中具有完全解决的HLA等位基因和预治疗的HIV-1病毒载量(VL),初级的四个AARS发现了兴趣(成熟HLA-B蛋白的位置63,97,116和245),用于解释这些群组的设定点V1中的8.1%和15.8%(p = .024和7.5 x 10(-6) , 分别)。之前未报告的两个AARS(HLA-B中的167s和HLA-C中的116F)也显示出与VL相对一致的关联(调整的P = .009-.069),而还注意到许多人口特定的关联(假发现率&lt ; 0.05)。在抗原呈现的结构基础之前,邻近的AAR变体中,邻近AAR​​变体之间的广泛和往往较强烈的联系不平衡呼吁在各种群体中进行更广泛的AAR单倍型分析。

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