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The polymorphisms of human leukocyte antigen loci may contribute to the susceptibility and severity of severe aplastic anemia in Chinese patients

机译:人类白细胞抗原基因座的多态性可能导致中国再生障碍性贫血的易感性和严重性

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摘要

The human leukocyte antigen (HLA) system has been reported to be involved in the development of aplastic anemia (AA). We compared and analyzed HLA-A, B, C, DRB1 and DQB1 alleles in 96 Chinese severe AA (SAA) patients to those in 600 healthy people chosen randomly from the China Marrow Donor Program to investigate the association of HLA class I and II allele polymorphisms with disposition of SAA and its severity degree in Chinese population. The DNA of patients was extracted and HLA high-resolution genotyping was conducted using polymerase chain reaction-sequence based typing technique. The gene frequencies of A*02:01, A*02:06, B*13:01, DRB1*07:01, DRB1*09:01, DRB1*15:01 and DQB1*06:02 in SAA patients were significantly higher than in controls (all P0.05), while the allelic frequencies of A*02:07, A*11:01 and B*40:01 were notably lower in SAA patients than those in the controls (P=0.001, 0.002, 0.005, respectively). Comparison among different severity of SAA groups exhibited significant increases of DRB1*15:01 (P=0.027) and DQB1*06:02 (P=0.013), but obviously lower frequencies of B*46:01 (P=0.023) and DRB1*09:01 (P=0.020) in non-VSAA patients than in VSAA patients. Thus, our results identified several risk and protective HLA alleles for Chinese SAA patients. Moreover, DRB1*15:01, DQB1*06:02, B*46:01 and DRB1*09:01 may be associated with severity of SAA.
机译:据报道,人类白细胞抗原(HLA)系统参与了再生障碍性贫血(AA)的发展。我们比较和分析了96名中国严重AA(SAA)患者与从中国骨髓捐赠者计划中随机选择的600名健康人的HLA-A,B,C,DRB1和DQB1等位基因,以研究HLA I和II类等位基因的关联SAA的多态性及其在中国人群中的严重程度提取患者的DNA,并使用基于聚合酶链反应序列的分型技术进行HLA高分辨率基因分型。 SAA患者中A * 02:01,A * 02:06,B * 13:01,DRB1 * 07:01,DRB1 * 09:01,DRB1 * 15:01和DQB1 * 06:02的基因频率显着SAA患者的A * 02:07,A * 11:01和B * 40:01的等位基因频率显着低于对照组(P均<0.05)(P = 0.001,0.002) ,分别为0.005)。不同严重程度SAA组之间的比较显示DRB1 * 15:01(P = 0.027)和DQB1 * 06:02(P = 0.013)显着增加,但B * 46:01(P = 0.023)和DRB1的出现频率明显降低*非VSAA患者的* 09:01(P = 0.020)比VSAA患者高。因此,我们的结果确定了中国SAA患者的几种危险和保护性HLA等位基因。此外,DRB1 * 15:01,DQB1 * 06:02,B * 46:01和DRB1 * 09:01可能与SAA的严重程度相关。

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