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HLA等位基因、单倍型频率及其与血液系统疾病的关联:来自埃及1550个家庭的报告,这些家庭的患者接受了异基因骨髓移植

HLA alleles, haplotypes frequencies, and their association with hematological disorders: a report from 1550 families whose patients underwent allogeneic bone marrow transplantation in Egypt.

作者信息

ElNahass Yasser, Mekky Nourhan, Abdelfattah Nabil M, Abdelfattah Raafat, Samra Mohamed, Fahmy Omar A, Fathy Gamal, Elmetnawy Wafaa, Sabet Salwa, Bassiouny Heba, Nader Heba, ElHaddad Alaa, Mahmoud H K

机构信息

National Cancer Institute, Cairo University, Cairo, Egypt.

Nasser Institute, Ministry of Health, Cairo, Egypt.

出版信息

Immunogenetics. 2024 Aug;76(4):243-260. doi: 10.1007/s00251-024-01343-x. Epub 2024 Jun 21.

Abstract

HLA alleles are representative of ethnicities and may play important roles in predisposition to hematological disorders. We analyzed DNA samples for HLA-A, -B, -C, -DRB1, and -DQB1 loci, from 1550 patients and 4450 potential related donors by PCR-SSO (Polymerase chain reaction sequence-specific oligonucleotides) and estimated allele frequencies in donors and patients from 1550 families who underwent bone marrow transplantation (BMT) in Egypt. We also studied the association between HLA allele frequencies and incidence of acute myeloid leukemia, acute lymphoblastic leukemia, and severe aplastic anemia. The most frequently observed HLA class I alleles were HLA- A01:01 (16.9%), A02:01 (16.1%), B41:01 (8.7%), B49:01 (7.3%), C06:02 (25.1%), and C07:01 (25.1%), and the most frequently observed class II alleles were HLA-DRB111:01 (11.8%), DRB103:01 (11.6%), DQB103:01 (27.5%), and DQB105:01 (18.9%). The most frequently observed haplotypes were A33:01~B14:02 ~ DRB101:02 (2.35%) and A01:01B*52:01DRB115:01 (2.11%). HLA-DRB107:01 was associated with higher AML odds (OR, 1.26; 95% CI, 1.02-1.55; p = 0.030). Only HLA-B38 antigen showed a trend towards increased odds of ALL (OR, 1.52; 95% CI, 1.00-2.30; p = 0.049) HLA-A02:01, -B14:02, and -DRB115:01 were associated with higher odds of SAA (A02:01: OR, 1.35; 95% CI, 1.07-1.70; p = 0.010; B14:02: OR, 1.43; 95% CI, 1.06-1.93; p = 0.020; DRB115:01: OR, 1.32; 95% CI, 1.07-1.64; p = 0.011). This study provides estimates of HLA allele and haplotype frequencies and their association with hematological disorders in an Egyptian population.

摘要

人类白细胞抗原(HLA)等位基因具有种族代表性,可能在血液系统疾病的易感性中发挥重要作用。我们通过聚合酶链反应序列特异性寡核苷酸(PCR - SSO)分析了1550例患者和4450例潜在相关供体的HLA - A、- B、- C、- DRB1和- DQB1基因座的DNA样本,并估计了埃及1550个接受骨髓移植(BMT)家庭中供体和患者的等位基因频率。我们还研究了HLA等位基因频率与急性髓系白血病、急性淋巴细胞白血病和重型再生障碍性贫血发病率之间的关联。最常观察到的HLA I类等位基因是HLA - A01:01(16.9%)、A02:01(16.1%)、B41:01(8.7%)、B49:01(7.3%)、C06:02(25.1%)和C07:01(25.1%),最常观察到的II类等位基因是HLA - DRB111:01(11.8%)、DRB103:01(11.6%)、DQB103:01(27.5%)和DQB105:01(18.9%)。最常观察到的单倍型是A33:01~B14:02 ~ DRB101:02(2.35%)和A01:01B*52:01DRB115:01(2.11%)。HLA - DRB107:01与急性髓系白血病的较高发病几率相关(比值比[OR],1.26;95%置信区间[CI],1.02 - 1.55;p = 0.030)。仅HLA - B38抗原显示出急性淋巴细胞白血病发病几率增加的趋势(OR,1.52;95% CI,1.00 - 2.30;p = 0.0 49)。HLA - A02:01、- B14:02和- DRB115:01与重型再生障碍性贫血的较高发病几率相关(A02:01:OR,1.35;95% CI,1.07 - 1.70;p = 0.010;B14:02:OR,1.43;95% CI,1.06 - 1.93;p = 0.020;DRB115:01:OR,1.32;95% CI,1.07 - 1.64;p = 0.011)。本研究提供了埃及人群中HLA等位基因和单倍型频率及其与血液系统疾病关联的估计值。

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