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在东南亚发现与HIV共受体功能降低相关的新型CCR5变体。

New CCR5 variants associated with reduced HIV coreceptor function in southeast Asia.

作者信息

Capoulade-Métay Corinne, Ma Liying, Truong Lien X, Dudoit Yasmine, Versmisse Pierre, Nguyen Ngai V, Nguyen Marie, Scott-Algara Daniel, Barré-Sinoussi Françoise, Debré Patrice, Bismuth Georges, Pancino Gianfranco, Theodorou Ioannis

机构信息

INSERM U543, CHU Pitié-Salpétrière, Institut Cochin, Paris, France.

出版信息

AIDS. 2004 Nov 19;18(17):2243-52. doi: 10.1097/00002030-200411190-00004.

Abstract

BACKGROUND

Despite multiple exposure to HIV-1, some individuals remain uninfected. This resistance has been associated with homozygosity for a 32 base pair deletion in the gene for the CCR5 receptor. This variant occurs frequently in Caucasians but is extremely rare in Asians or Africans.

OBJECTIVE

To identify variations in CCR5 receptor gene that affect susceptibility to HIV infection in non-Caucasians.

METHODS

CCR5 coding region polymorphisms were screened in three groups of Vietnamese subjects: 47 HIV-1 infected intravascular drug users, 50 highly HIV-1-exposed but seronegative intravascular drug users and 37 HIV-1-unexposed seronegative individuals. DNA was analysed by denaturing high performance liquid chromatography; this was followed by examination of the biochemical and HIV coreceptor properties of the coding regions.

RESULTS

Five CCR5 coding region variants were identified in this Vietnamese population. The S185R, I254T and C269F mutations have not been previously described; G106R and R223Q have already been found in other Asian populations, but the functional properties of G106R is not known. These variants differed in biochemical and HIV coreceptor properties. S185R and I254T variants had receptor and coreceptor activities comparable to that of the wild type, whereas C269F and G106R behaved differently. This latter pair are poorly expressed at the cell surface, weakly bind macrophage inflammatory protein 1beta (CCL4) and RANTES (CCL5), and display reduced HIV-1 coreceptor efficiency.

CONCLUSIONS

Among the five CCR5 variants found in this Vietnamese population, G106R and C269F displayed significant modifications of their receptor and coreceptor properties, which may contribute to susceptibility to HIV-1 infection and/or disease progression within this population.

摘要

背景

尽管多次接触HIV-1,但仍有一些个体未被感染。这种抵抗力与CCR5受体基因中32个碱基对缺失的纯合性有关。这种变异在白种人中很常见,但在亚洲人或非洲人中极为罕见。

目的

确定影响非白种人对HIV感染易感性的CCR5受体基因变异。

方法

在三组越南受试者中筛选CCR5编码区多态性:47名感染HIV-1的血管内吸毒者、50名HIV-1高暴露但血清学阴性的血管内吸毒者和37名未暴露于HIV-1的血清学阴性个体。通过变性高效液相色谱分析DNA;随后检查编码区的生化和HIV共受体特性。

结果

在该越南人群中鉴定出5种CCR5编码区变异。S185R、I254T和C269F突变此前未被描述;G106R和R223Q已在其他亚洲人群中发现,但G106R的功能特性尚不清楚。这些变异在生化和HIV共受体特性方面存在差异。S185R和I254T变异体的受体和共受体活性与野生型相当,而C269F和G106R的表现不同。后一对在细胞表面表达较差,与巨噬细胞炎性蛋白1β(CCL4)和RANTES(CCL5)的结合较弱,并显示出HIV-1共受体效率降低。

结论

在该越南人群中发现的5种CCR5变异体中,G106R和C269F的受体和共受体特性有显著改变,这可能导致该人群对HIV-1感染和/或疾病进展的易感性。

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