Azarpira Negar, Nikeghbalian Saman, Geramizadeh Bita, Darai Masumeh
Organ Transplant Research Center, Nemazi Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.
Mol Biol Rep. 2010 Jan;37(1):21-5. doi: 10.1007/s11033-009-9487-5. Epub 2009 Feb 28.
Glutathione-S-transferase (GST) has a major protective role against free radicals and plays a vital role in phase II of biotransformation of many substances. In liver transplantation, reperfusion injury, calcineurin drug consumption and infection produce free radicals that cause tissue injury and organ damage. Genetic variations of GST may influence individual susceptibility to some diseases associated with the deleterious effects of oxidative metabolism. Although it is well known that the rejection is an immunological process, however, in this study, we have investigated the gene frequency and relationship between human GST gene polymorphism and rejection in liver transplant recipients. We have assessed 51 liver transplant recipients from Shiraz, South of Iran. The GSTT1 and GSTM1 genotypes were identified by polymerase chain reaction (PCR). The gene frequency of GSTM1 and GSTT1 polymorphism were evaluated. We observed that GSTM1 null genotype was present in 68.62% of the liver transplant recipients while GSTT1 null genotype was present in 37.25% of the liver transplant subjects. There was a trend between increasing age and acute rejection episode. No statistically significant correlation was present between GSTM1 null and GSTT1 null genotypes with an acute rejection episode in transplant recipients. No relationship was observed between GST genotypes and acute rejection. It is likely that development and progression of rejection are determined by genes which is involved in immunological pathways rather than genes that is participated in free radicals destruction. However, these findings need to be confirmed in a larger series of patients.
谷胱甘肽 - S - 转移酶(GST)对自由基具有主要的保护作用,并且在许多物质的生物转化第二阶段中发挥着至关重要的作用。在肝移植中,再灌注损伤、钙调神经磷酸酶药物的使用以及感染会产生自由基,进而导致组织损伤和器官损害。GST的基因变异可能会影响个体对某些与氧化代谢有害影响相关疾病的易感性。虽然众所周知排斥反应是一个免疫过程,然而,在本研究中,我们调查了人类GST基因多态性与肝移植受者排斥反应之间的基因频率及关系。我们评估了来自伊朗南部设拉子的51名肝移植受者。通过聚合酶链反应(PCR)鉴定GSTT1和GSTM1基因型。评估了GSTM1和GSTT1多态性的基因频率。我们观察到,68.62%的肝移植受者存在GSTM1无效基因型,而37.25%的肝移植受者存在GSTT1无效基因型。年龄增长与急性排斥反应发作之间存在一种趋势。移植受者中GSTM1无效和GSTT1无效基因型与急性排斥反应发作之间不存在统计学上的显著相关性。未观察到GST基因型与急性排斥反应之间的关系。排斥反应的发生和进展可能由参与免疫途径的基因决定,而非参与自由基破坏的基因。然而,这些发现需要在更大规模的患者系列中得到证实。