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HIV感染抗性的遗传学:共受体及共受体配体的作用

Genetics of resistance to HIV infection: Role of co-receptors and co-receptor ligands.

作者信息

Arenzana-Seisdedos Fernando, Parmentier Marc

机构信息

Unité de Pathogénie Virale Moléculaire, Département de Virologie, INSERM, Institut Pasteur, 28 rue du Dr Roux, 75724 Paris cedex, France.

出版信息

Semin Immunol. 2006 Dec;18(6):387-403. doi: 10.1016/j.smim.2006.07.007. Epub 2006 Sep 15.

Abstract

Susceptibility to HIV infection and AIDS progression is variable among individuals and populations, and in part genetically determined. Genetic variants of genes encoding HIV co-receptors and their chemokine ligands have been described, and some of these variants were associated with resistance to HIV infection and/or disease progression. We review here the reported data regarding the variants of the CCR5, CCR2, CX3CR1, MIP-1alpha/CCL3, MIP-1beta/CCL4, RANTES/CCL5 and SDF-1/CXCL12 genes. The Delta32 deletion mutant of CCR5, resulting in a non-functional receptor not reaching the cell surface, is unambiguously associated with strong, although incomplete, resistance to HIV infection for homozygotes, and retarded progression for heterozygotes. Specific haplotypes encompassing the CCR5 and CCR2 loci, and the copy number of the CCL3L1 gene, have also been convincingly correlated with delayed progression. For other gene variants, involving CXCL12/SDF-1 and CX3CR1, conclusive evidence for their relevance in the frame of HIV susceptibility is still lacking.

摘要

个体和人群对HIV感染及艾滋病进展的易感性存在差异,部分由基因决定。已发现编码HIV共受体及其趋化因子配体的基因存在遗传变异,其中一些变异与对HIV感染的抗性和/或疾病进展有关。我们在此综述有关CCR5、CCR2、CX3CR1、MIP-1α/CCL3、MIP-1β/CCL4、RANTES/CCL5和SDF-1/CXCL12基因变异的报道数据。CCR5的Delta32缺失突变体导致无功能的受体无法到达细胞表面,对于纯合子,它与对HIV感染的强抗性(尽管不完全)明确相关,对于杂合子则与疾病进展延迟相关。包含CCR5和CCR2基因座的特定单倍型以及CCL3L1基因的拷贝数也与疾病进展延迟有令人信服的关联。对于涉及CXCL12/SDF-1和CX3CR1的其他基因变异,仍缺乏关于它们在HIV易感性方面相关性的确凿证据。

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