儿童早期自身免疫性中性粒细胞减少症患者的HNA特异性及其与HLA-DRB1和-DQB1的相关性

Kirstine Kløve-Mogensen , Rudi Steffensen , Hans Linde Nielsen , Tania Nicole Masmas , Andreas Glenthøj , Christina Friis Jensen , Thure Mors Haunstrup , Paul Ratcliffe , Petter Höglund , Henrik Hasle , Kaspar René Nielsen
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引用次数: 0

摘要

儿童早期的自身免疫性中性粒细胞减少症(AIN)是由中性粒细胞膜上的抗原自身抗体引起的。人类白细胞抗原(HLA)以前曾与AIN相关。本研究调查了160名抗体阳性患者的HLA-DRB1和HLA-DQB1等位基因,并与1000名对照组进行了比较。观察到DRB1*10、DRB1*14、DRB1*6和DQB1*05的风险增加,DRB1*04、DRB1*13和DQB1*03的风险降低。风险较高的单倍型包括:DRB1*10/DQB1*05、DRB1*14/DQB1*05和DRB1*16/DQB1*05,而DRB1*04/DQB1*03、DRB1*07/DQB1*2和DRB1*13/DQB1*06与风险较低相关。抗HNA-1a特异性抗体阳性患者和广泛反应性抗FcγRIIIb抗体阳性患者的相关HLA-DRB1和-DQB1不同。DRB1*01、DRB1*04和DQB1*03仅与抗HNA-1a阳性相关,DRB1*10仅限于广泛反应性抗FcγRIIIb阳性。AIN与HLA-DRB1和-DQB1等位基因和单倍型之间的强相关性表明它们在易感性或保护性中发挥作用。FcγRIIIb抗体特异性的不同关联可能表明疾病的异质性。
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HNA specificity and association to HLA-DRB1 and -DQB1 in patients with autoimmune neutropenia of early childhood

Autoimmune neutropenia (AIN) of early childhood is caused by autoantibodies against antigens on the neutrophil membrane. Human leukocyte antigens (HLA) have previously been associated with AIN. This study investigated HLA-DRB1 and HLA-DQB1 alleles in 160 antibody positive patients and compared with 1000 controls. Increased risk was observed for DRB1*10, DRB1*14, DRB1*16 and DQB1*05, and lower risk for DRB1*04, DRB1*13 and DQB1*03. Haplotypes with higher risk included: DRB1*10/DQB1*05, DRB1*14/DQB1*05 and DRB1*16/DQB1*05, while DRB1*04/DQB1*03, DRB1*07/DQB1*02, and DRB1*13/DQB1*06 were associated with lower risk. Associated HLA-DRB1 and –DQB1 differed between patients positive for anti-HNA-1a-specific antibodies and patients positive for broad reactive anti-FcγRIIIb antibodies. DRB1*01, DRB1*04 and DQB1*03 was only associated for anti-HNA-1a positive, and DRB1*10 was restricted to broad reactive anti-FcγRIIIb positive. Strong association between AIN and HLA-DRB1 and -DQB1 alleles and haplotypes suggested that they play a role in susceptibility or protection. Different associations regarding FcγRIIIb antibody specificities could indicate disease heterogeneity.

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