首页> 美国卫生研究院文献>Journal of Virology >Clade-Specific Evolution Mediated by HLA-B*57/5801 in Human Immunodeficiency Virus Type 1 Clade A1 p24
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Clade-Specific Evolution Mediated by HLA-B*57/5801 in Human Immunodeficiency Virus Type 1 Clade A1 p24

机译:HLA-B * 57/5801在人类免疫缺陷病毒1型进化枝A1 p24中介导的进化枝特定进化

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摘要

HLA-B*57-mediated selection pressure leads to a typical escape pathway in human immunodeficiency virus type 1 (HIV-1) CD8 epitopes such as TW10. Whether this T242N pathway is shared by all clades remains unknown. We therefore assessed the nature of HLA-B*57 selection in a large, observational Kenyan cohort where clades A1 and D predominate. While T242N was ubiquitous in clade D HLA-B*57+ subjects, this mutation was rare (15%) in clade A1. Instead, P243T and I247L were selected by clade A1-infected HLA-B*57 subjects but not by HLA-B*5801+ subjects. Our data suggest that clade A1 consensus proline at Gag residue 243 might represent an inherent block to T242N escape in clade A1. We confirmed immunologically that P243T and I247L likely represent escape mutations. HLA-B*57 evolution also differed between clades in the KF11 and IW9 epitopes. A better understanding of clade-specific evolution is important for the development of HIV vaccines in regions with multiple clades.
机译:HLA-B * 57介导的选择压力导致人类免疫缺陷病毒1型(HIV-1)CD8表位(例如TW10)中的典型逃逸途径。该T242N途径是否被所有进化枝共享仍然未知。因此,我们在肯尼亚A1和D进化枝占优势的大型观察性队列研究中评估了HLA-B * 57选择的性质。尽管T242N在进化枝D HLA-B * 57 + 受试者中无处不在,但这种突变在进化枝A1中很少见(15%)。而是,由进化枝A1感染的HLA-B * 57受试者选择了P243T和I247L,但没有由HLA-B * 5801 + 受试者选择。我们的数据表明,在Gag残基243上的进化枝A1共有脯氨酸可能代表了进化枝A1中T242N逃逸的固有障碍。我们通过免疫学证实,P243T和I247L可能代表逃逸突变。 HLA-B * 57进化在KF11和IW9表位的进化枝之间也有所不同。更好地了解进化枝特异性进化对于在具有多个进化枝的地区开发HIV疫苗很重要。

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