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突尼斯丙型肝炎病毒感染血液透析患者趋化因子及其受体基因多态性

Chemokine and chemokine receptor gene polymorphism in Tunisian hemodialysis patients with HCV infection.

作者信息

Ksiaa Cheikh Rouhou Leila, Gorgi Yousr Lakhoua, Skhiri Hajer Aounallah, Aouadi Houda, Ayed Salwa Jendoubi, Sfar Imen, Ayed Khaled, Ben Abdallah Taieb

机构信息

Immunology Research Laboratory of Kidney Transplantation and Immunopathology (Laboratoire de Recherche: LR03SP01), Charles Nicolle Hospital, Tunisia.

出版信息

Arab J Nephrol Transplant. 2011 Sep;4(3):117-24. doi: 10.4314/ajnt.v4i3.71023.

Abstract

INTRODUCTION

Our aim was to investigate the possibility of a significant relationship between chemokines and chemokine receptor genes polymorphisms and the spontaneous clearance or the persistence of HCV infection.

METHODS

A total of 96 hemodialysis (HD) patients infected with HCV were classified into two groups: G1 included 73 patients with persistently positive HCV-RNA and G2 included 23 HD patients who have spontaneously eliminated the virus. The control group consisted of 170 healthy blood donors. All subjects were genotyped for CCR5 ?32, CCR5 (-59029) A/G, CCR2 (64Ile) and MCP-1(-2518) A/G gene polymorphisms.

RESULTS

Our results showed a statistically significant increased frequencies of the CCR2 (64Ile) and the (-59029) CCR5 A alleles in patients infected with HCV (22.1% and 35.9%) compared to G1 (24.3% and 40.6%) and compared to controls (14.4% and 20%). We also observed a lower frequency of the MCP-1 G allele and a greater frequency of the CCR5?32 variant in G2 (15.2% and 6.5%) compared to G1 (22.6% and 1.4%) that was not statistically significant. However, adjustment for known covariates (age, gender and HCV genotypes) didn't confirm the results of univariate analysis.

CONCLUSION

In conclusion, our study suggests a possible role for some of the studied chemokines polymorphisms in the spontaneous clearance or persistence of HCV infection in Tunisian population. These results should be further investigated by a prospective cohort studies and large population-based studies.

摘要

引言

我们的目的是研究趋化因子和趋化因子受体基因多态性与丙型肝炎病毒(HCV)感染的自发清除或持续存在之间是否存在显著关联。

方法

总共96例感染HCV的血液透析(HD)患者被分为两组:G1组包括73例HCV-RNA持续阳性的患者,G2组包括23例已自发清除病毒的HD患者。对照组由170名健康献血者组成。对所有受试者进行CCR5 Δ32、CCR5(-59029)A/G、CCR2(64Ile)和MCP-1(-2518)A/G基因多态性的基因分型。

结果

我们的结果显示,与G1组(24.3%和40.6%)以及对照组(14.4%和20%)相比,感染HCV的患者中CCR2(64Ile)和CCR5(-59029)A等位基因的频率在统计学上显著增加(分别为22.1%和35.9%)。我们还观察到,与G1组(22.6%和1.4%)相比,G2组中MCP-1 G等位基因的频率较低,CCR5 Δ32变异体的频率较高(分别为15.2%和6.5%),但差异无统计学意义。然而,对已知协变量(年龄、性别和HCV基因型)进行调整后,未证实单因素分析的结果。

结论

总之,我们的研究表明,在突尼斯人群中,某些研究的趋化因子多态性可能在HCV感染的自发清除或持续存在中发挥作用。这些结果应通过前瞻性队列研究和基于大人群的研究进一步调查。

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