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首页> 外文期刊>Macedonian Journal of Medical Sciences >Killer Cell Immunoglobulin-Like Receptor Genes Polymorphisms in Macedonian Patients with Haematological Malignancies
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Killer Cell Immunoglobulin-Like Receptor Genes Polymorphisms in Macedonian Patients with Haematological Malignancies

机译:马其顿血液系统恶性肿瘤患者的杀伤细胞免疫球蛋白样受体基因多态性

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Aim: The aim of this study was to examine the gene frequencies of 16 KIR genes and pseudogenes (KIR2DL1, KIR2DL2, KIR2DL3, KIR2DL4, KIR2DL5, KIR3DL1, KIR3DL2, KIR3DL3, KIR2DS1, KIR2DS2, KIR2DS3, KIR2DS4, KIR2DS5, KIR3DS1, KIR2DP1, and KIR3DP1) and KIR genotypes in Macedonian patients with haematological malignancies, to compare them with the corresponding frequencies of healthy Macedonians and to analyse eventual association of specific genes or genotypes with the studied haematological diseases.Material and Methods: The study included 63 patients of which 40 had acute myeloblastic leukaemia (63.5%), 11 (17.5%) had chronic myeloid leukaemia, 8 (12.7%) acute lymphoblastic leukaemia, 2 (3.17%) non-Hodgkin Lymphoma, 1 (1.59%) aplastic anemia, and 1 (1.59%) chronic lymphocytic leukaemia.Results: Comparison of KIR gene frequencies between the 63 patients and healthy Macedonians reveals statistically significant difference for KIR3DL2 (F=1 in the control group, and 0.95 in the patients group, p=0.001). Another statistically significant difference was observed for the frequency of Bx3 and Bx439 genotypes both found more often in patients group (P=0.017 and P= 0.009, respectively).Conclusion: Further analysis, involving larger series of patients and targeted at the ligands of the KIRs are needed in order to determine a certain KIR gene and/or genotype as either predisposing, or protecting factor for haematological malignancy in patients from Republic of Macedonia.
机译:目的:本研究的目的是检查16种KIR基因和假基因的基因频率(KIR2DL1,KIR2DL2,KIR2DL3,KIR2DL4,KIR2DL5,KIR3DL1,KIR3DL2,KIR3DL3,KIR2DS1,KIR2DS2,KIR2DS3,KIR2DS4,KIR2DS4,和KIR3DP1)和KIR基因型在马其顿血液系统恶性肿瘤患者中进行比较,以将其与健康马其顿人的相应频率进行比较,并分析特定基因或基因型与所研究的血液疾病的最终关联。材料与方法:该研究包括63位患者40例急性粒细胞白血病(63.5%),11例(17.5%)慢性粒细胞白血病,8例(12.7%)急性淋巴细胞白血病,2例(3.17%)非霍奇金淋巴瘤,1例(1.59%)再生障碍性贫血和1例结果:63例患者和健康的马其顿人之间的KIR基因频率比较显示,KIR3DL2在统计学上有显着差异(对照组为F = 1,患者组为0.95) ,p = 0.001)。在患者组中发现的Bx3和Bx439基因型的频率也存在另一个统计学上的显着差异(分别为P = 0.017和P = 0.009)。结论:进一步的分析,涉及更大系列的患者,针对Bx3和Bx439基因型的配体。为了确定某些KIR基因和/或基因型是马其顿共和国患者血液恶性肿瘤的诱发因素或保护因素,需要使用KIR。

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