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HLA class II antigens and haplotypes associated with susceptibility of leukemias and myelodysplastic syndrome

机译:HLA II类抗原和单体型与白血病和骨髓增生异常综合症的易感性相关

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Genetical and environmental factors play an interactive role in the development of acute and chronic leukemias. HLA antigens have been considered as possible genetic risk factors. The aim of this work was to investigate a possible association between HLA class II polymorphisms and leukemias and myelodysplastic syndrome. In the present study we investigated HLA class II antigens, DR/DQ and DR51/DR52/DR53 haplotypes in 100 patients: 7 suffering from myelodysplastic syndrome (MDS),37 from acute lymphoblastic leukemia(ALL),32 from acute myeloid leukemia (AML) and 24 from chronic myeloid leukemia(CML). A panel of 210 healthy unrelated individuals of the same origin, from Vojvodina, served as controls. HLA phenotyping was performed by two color fluorescence method. In patients suffering from MDS was found a positive association with DR7(RR=2.598,EF=0.175) and DQ7(3)(RR=4.419, EF=0.632), while negative association was found for DR15(2)(RR=0.405, PF=0.172) and DQ6(1) (RR=0.889, PF=0,936).Positive association was found in the group of patients with ALL for DR7(RR=2.391,EF=0.688) and DQ2(RR=1.62, EF=0.15),while negative association was found with DQ5(1)(RR=0.075, PF=0.324). In the group of patients with AML, there were positive associations with DR11(5)(RR=1.732,EF=0.211),DQ2(RR= 1.594, EF=0.151) and DQ7(3) (RR=2.547,EF=0.266),while possible protective antigen was DQ5(1) (RR=0.107,RF=0.701). Higher RR than 1 and EF>0.15, in patients suffering from CML was found for DQ6(1)(RR=1.661,EF=0.232), while negative association was found for DR4 (RR=0.182,PF=0.155).Possible protective haplotype in this study was DR3DQ8(3) for patients suffering from AML(RR=0.007, PF=0.501).The distribution of DR53-DR53 haplotypes showed significant difference in male patients with ALL(6% vs 0.09%), while DR52-DR52 haplotype was significantly less frequent in male patients with CML (4% vs 20.47%) and female patients with MDS (1% vs 18.57%), respectively, in comparison to controls. We deduced that DR7 antigen in male patients with ALL has the greatest impact to the higher frequency of DR53-DR53 haplotype in this type of leukemia. The role of HLA antigens as risk factors for development of leukemias in our population was shown and furthermore it could be useful in clinical practice.
机译:遗传和环境因素在急性和慢性白血病的发展中起着相互作用的作用。 HLA抗原被认为是可能的遗传危险因素。这项工作的目的是调查HLA II类多态性与白血病和骨髓增生异常综合症之间的可能联系。在本研究中,我们调查了100位患者的HLA II类抗原,DR / DQ和DR51 / DR52 / DR53单倍型:7位患有骨髓增生异常综合症(MDS),37位急性淋巴细胞白血病(ALL),32位急性髓系白血病(AML) )和24来自慢性粒细胞白血病(CML)。来自伏伊伏丁那(Vojvodina)的210名相同血统的健康无关个体作为对照。通过两色荧光法进行HLA表型分析。在患有MDS的患者中发现与DR7(RR = 2.598,EF = 0.175)和DQ7(3)(RR = 4.419,EF = 0.632)呈正相关,而与DR15(2)(RR = 0.405)呈负相关。 ,PF = 0.172)和DQ6(1)(RR = 0.889,PF = 0,936)。在ALL患者中发现DR7(RR = 2.391,EF = 0.688)和DQ2(RR = 1.62,EF)呈正相关= 0.15),而发现与DQ5(1)呈负相关(RR = 0.075,PF = 0.324)。在AML患者组中,与DR11(5)(RR = 1.732,EF = 0.211),DQ2(RR = 1.594,EF = 0.151)和DQ7(3)(RR = 2.547,EF = 0.266)呈正相关),而可能的保护性抗原是DQ5(1)(RR = 0.107,RF = 0.701)。 DQ6(1)患CML的患者的RR高于1,EF> 0.15(RR = 1.661,EF = 0.232),而DR4呈负相关(RR = 0.182,PF = 0.155)。这项研究对AML患者的单倍型为DR3DQ8(3)(RR = 0.007,PF = 0.501)。在患有ALL的男性患者中,DR53-DR53单倍型的分布显示出显着差异(6%对0.09%),而DR52-与对照组相比,在患有CML的男性患者(分别为4%和20.47%)和具有MDS的女性患者(分别为1%和18.57%)中,DR52单倍型的发生率明显更低。我们推论,患有ALL的男性患者中的DR7抗原对这种类型的白血病中较高的DR53-DR53单倍型频率影响最大。已经显示出HLA抗原作为我们人群中白血病发展的危险因素的作用,并且其在临床实践中可能是有用的。

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