评价- 318C/T (RS5742909) CTLA4基因多态性对移植后肾功能的影响

Nevena Veljančić, V. Perovic
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引用次数: 0

摘要

蛋白CTLA-4(细胞毒性T淋巴细胞抗原-4)是一种在维持免疫稳态中起重要作用的分子。最近的研究明确证明CTLA-4对免疫反应有抑制作用。该基因具有多个单核苷酸多态性,可以改变基因活性,从而导致结构蛋白的改变。这种遗传变异与急性排斥反应和移植功能延迟有关,是肾移植成功的重要指标。目的:本研究的目的是评估CTLA4 (rs5742909)多态性与肾移植患者急性排斥反应和移植功能延迟的潜在关联。材料和方法:本横断面队列研究共纳入151例患者。采用实时聚合酶链反应确定基因型,然后评估其与急性排斥反应和移植延迟功能的关系。统计学显著性采用Pearson卡方检验和Fisher精确检验。结果:151例患者中基因型最多的是CC(80.8%),其次是CT(17.9%)和TT(1.3%)。C等位基因频率为89.7%,T等位基因频率为10.3%。CTLA4基因型和等位基因分布及其与急性排斥反应和移植延迟功能的相关性无统计学差异。C或T等位基因携带者的评估在移植后并发症方面无统计学差异。结论:本研究未发现-318C/T (rs5742909) CTLA4多态性与AR/DGF之间存在统计学意义的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the - 318C/T (RS5742909) CTLA4 gene polymorphism influence on kidney function after transplantation
Introduction: The protein CTLA-4 (Cytotoxic T Lymphocyte Antigen-4) is a molecule that plays a significant role in maintaining immunological homeostasis. Recent studies demonstrated an unequivocal proof that CTLA-4 has an inhibitory effect on immune response. This gene has been identified with several single nucleotide polymorphisms which could change gene activity, consequently leading to structural protein change. This genetic variability is associated with acute rejection and delayed graft function as important indicators of kidney transplantation success. Aim: The aim of this study was to evaluate the potential association of CTLA4 (rs5742909) polymorphisms with acute rejection and delayed graft function in patients with kidney transplant. Material and methods: A total of 151 patients were included in this cross-sectional cohort study. Real-time polymerase chain reaction was used to determine the genotype which was then evaluated in relation to acute rejection and delayed graft function. Statistical significance was analyzed by Pearson's Chi-square and Fisher's exact test. Results: The most frequent genotype among 151 patient was CC (80.8%), then CT (17.9%) and TT (1.3%). The frequency of C allele is 89.7% whereas the frequency of T allele is 10.3%. There was no statistically significant difference in CTLA4 genotype and allele distribution nor their linkage to acute rejection and delayed graft function. The evaluation of C or T allele carriers showed no statistically significant difference with respect to previously mentioned posttransplant complications. Conclusion: In this study, no statistically significant association between -318C/T (rs5742909) CTLA4 polymorphism and AR/DGF was found.
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