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与感染猿猴免疫缺陷病毒(SIV)的恒河猴生存时间相关的Mhc I类单倍型

Mhc class I haplotypes associated with survival time in simian immunodeficiency virus (SIV)-infected rhesus macaques.

作者信息

Sauermann U, Siddiqui R, Suh Y-S, Platzer M, Leuchte N, Meyer H, Mätz-Rensing K, Stoiber H, Nürnberg P, Hunsmann G, Stahl-Hennig C, Krawczak M

机构信息

Department of Virology and Immunology, German Primate Center, Leibniz Institute for Primate Research, Göttingen, Germany.

出版信息

Genes Immun. 2008 Jan;9(1):69-80. doi: 10.1038/sj.gene.6364448. Epub 2007 Dec 20.

Abstract

In both human immunodeficiency virus-infected humans and simian immunodeficiency virus (SIV)-infected macaques, genes encoded in the major histocompatibility complex (MHC) class I region are important determinants of disease progression. However, compared to the human human lymphocyte antigen complex, the macaque MHC region encodes many more class I genes. Macaques with the same immunodominant class I genes express additional Mhc genes with the potential to influence the disease course. We therefore assessed the association between of the Mhc class I haplotypes, rather than single gene variants, and survival time in SIV-infected rhesus macaques (Macaca mulatta). DNA sequence analysis and Mhc genotyping of 245 pedigreed monkeys identified 17 Mhc class I haplotypes that constitute 10 major genotypes. Among 81 vaccination-naive, SIV-infected macaques, 71 monkeys carried at least one Mhc class I haplotype encoding only MHC antigens that were incapable of inducing an effective anti-SIV cytotoxic T lymphocytes response. Study of these macaques enabled us to relate individual Mhc class I haplotypes to slow, medium and rapid disease progression. In a post hoc analysis, classification according to disease progression was found to explain at least 48% of the observed variation of survival time.

摘要

在人类免疫缺陷病毒感染的人类和猿猴免疫缺陷病毒(SIV)感染的猕猴中,主要组织相容性复合体(MHC)I类区域编码的基因是疾病进展的重要决定因素。然而,与人类淋巴细胞抗原复合体相比,猕猴MHC区域编码的I类基因要多得多。具有相同免疫显性I类基因的猕猴会表达额外的Mhc基因,这些基因有可能影响疾病进程。因此,我们评估了Mhc I类单倍型而非单基因变体与SIV感染的恒河猴(猕猴)生存时间之间的关联。对245只系谱猴进行的DNA序列分析和Mhc基因分型确定了17种Mhc I类单倍型,它们构成了10种主要基因型。在81只未接种疫苗、感染SIV的猕猴中,71只猕猴携带至少一种仅编码无法诱导有效抗SIV细胞毒性T淋巴细胞反应的MHC抗原的Mhc I类单倍型。对这些猕猴的研究使我们能够将个体Mhc I类单倍型与疾病的缓慢、中等和快速进展联系起来。在事后分析中,发现根据疾病进展进行的分类至少可以解释观察到的生存时间变化的48%。

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