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TNF-α-238 和 PDCD1-7209 多态性与 HIV-1 长期非进展性感染的新遗传关联。

Novel genetic association of TNF-α-238 and PDCD1-7209 polymorphisms with long-term non-progressive HIV-1 infection.

机构信息

Department of Surgery, Medicine, Dentistry and Morphological Sciences, University of Modena and Reggio Emilia, Via Campi 287, 41125 Modena, Italy.

出版信息

Int J Infect Dis. 2013 Oct;17(10):e845-50. doi: 10.1016/j.ijid.2013.01.003. Epub 2013 Feb 10.

Abstract

OBJECTIVES

About 2-5% of HIV-1-infected subjects, defined as long-term non-progressors (LTNPs), remain immunologically stable for a long time without treatment. The factors governing this condition are known only in part, and include genetic factors. Thus, we studied 20 polymorphisms of 15 genes encoding proinflammatory and immunoregulatory cytokines, chemokines and their receptors, genes involved in apoptosis, and the gene HCP5.

METHODS

We analyzed 47 Caucasian LTNPs infected for >9 years, compared with 131 HIV-1-infected Caucasian patients defined as 'usual progressors'. The genotypes were determined by methods based upon PCR, and the statistical analysis was performed by univariate logistic regression.

RESULTS

The well-known CCR5Δ32 del32 allele, the cell death-related TNF-α-238 A and PDCD1-7209 T alleles, and HCP5 rs2395029 G, a non-coding protein associated with the HLA-B*5701, were found positively associated with the LTNP condition. No association was observed for other single nucleotide polymorphisms (SDF-1-801, IL-10-592, MCP-1-2518, CX3CR1 V249I, CCR2V64I, RANTES-403, IL-2-330, IL-1β-511, IL-4-590, FASL IVS3nt-169, FAS-670, FAS-1377, FASL IVS2nt-124, PDCD1-7146, MMP-7-181, and MMP7-153).

CONCLUSIONS

The novel genetic associations between allelic variants of genes TNF-α-238 and PDCD1-7209 with the LTNP condition underline the importance of host genetic factors in the progression of HIV-1 infection and in immunological preservation.

摘要

目的

约 2-5%的 HIV-1 感染者为长期无进展者(LTNP),他们在未经治疗的情况下长期保持免疫稳定。目前仅部分了解决定这种情况的因素,包括遗传因素。因此,我们研究了编码前炎症和免疫调节细胞因子、趋化因子及其受体的 15 个基因中的 20 个多态性、凋亡相关基因以及 HCP5 基因。

方法

我们分析了 47 名感染超过 9 年的高加索 LTNP,与 131 名感染 HIV-1 的高加索患者(定义为“通常进展者”)进行了比较。采用基于 PCR 的方法确定基因型,并通过单变量 logistic 回归进行统计分析。

结果

已知的 CCR5Δ32del32 等位基因、细胞死亡相关的 TNF-α-238A 和 PDCD1-7209T 等位基因以及与 HLA-B*5701 相关的非编码蛋白 HCP5rs2395029G 与 LTNP 状态呈正相关。未观察到其他单核苷酸多态性(SDF-1-801、IL-10-592、MCP-1-2518、CX3CR1 V249I、CCR2V64I、RANTES-403、IL-2-330、IL-1β-511、IL-4-590、FASL IVS3nt-169、FAS-670、FAS-1377、FASL IVS2nt-124、PDCD1-7146、MMP-7-181 和 MMP7-153)存在相关性。

结论

基因 TNF-α-238 和 PDCD1-7209 等位基因变异与 LTNP 状态之间的新遗传关联强调了宿主遗传因素在 HIV-1 感染进展和免疫保护中的重要性。

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