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首页> 外文期刊>Iranian Journal of Immunology >Association of CCR5-59029 A/G and CCR2-V64I Variants with Renal Allograft Survival
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Association of CCR5-59029 A/G and CCR2-V64I Variants with Renal Allograft Survival

机译:CCR5-59029 A / G和CCR2-V64I变体与同种异体肾移植存活率的关联

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Background: Despite advances in the medical care of renal transplant recipients which have led to an improvement in allograft survival, renal allograft rejection is still a major ob-stacle to successful organ transplantation. Understanding the mechanisms contributing to allograft rejection will be of great importance for the development of efficient antirejection strategies. Objective: The aim of current investigation was to study the impact of polymor-phisms of CCR5Δ32, CCR5- 59029 A/G and CCR2-V64I on renal allograft survival. Methods: Using PCR and PCR-RFLP methods in 84 renal transplant recipients, the influ-ence of CCR5Δ32, CCR5- 59029 A/G and CCR2-V64I polymorphisms on renal allograft survival in two rejector and non-rejector groups were examined. Rejector group was de-fined as having rejection before 1 year and non-rejector group had stable graft function at least for 5 years. Results: Significant reductions were found in the risk of renal transplant rejection in recipients possessing the CCR2-64I (A) allele (p=0.03) or 59029-A allele (p=0.03) compared to non-rejector group. There were no significant differences in the fre-quency of CCR5Δ32 polymorphism in rejector group compared to non-rejector group (p0.05). Conclusion: It was possible to conclude that the chemokine receptors CCR2-V64I (A) and CCR5- 59029 A alleles may influence renal allograft survival.
机译:背景:尽管肾移植接受者的医疗保健有所进步,导致同种异体移植存活率提高,但肾同种异体移植排斥仍然是成功器官移植的主要障碍。理解导致同种异体排斥反应的机制对于开发有效的抗排斥策略非常重要。目的:目前的研究目的是研究CCR5Δ32,CCR5-59029 A / G和CCR2-V64I多态性对同种异体肾移植存活的影响。方法:采用PCR和PCR-RFLP方法在84例肾移植受者中,观察CCR5Δ32,CCR5-59029 A / G和CCR2-V64I多态性对两个排斥组和非排斥组肾移植存活的影响。拒绝组定义为1年之前有排斥反应,非拒绝组至少5年内具有稳定的移植物功能。结果:与非排斥组相比,具有CCR2-64I(A)等位基因(p = 0.03)或59029-A等位基因(p = 0.03)的接受者的肾移植排斥风险显着降低。与非排斥组相比,排斥组CCR5Δ32多态性的频率无显着差异(p> 0.05)。结论:可以得出以下结论:趋化因子受体CCR2-V64I(A)和CCR5- 59029 A等位基因可能影响肾移植的存活。

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