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HLA - DRw2与自身免疫性血小板减少性紫癜的关联。

Association of HLA-DRw2 with autoimmune thrombocytopenic purpura.

作者信息

Karpatkin S, Fotino M, Gibofsky A, Winchester R J

出版信息

J Clin Invest. 1979 May;63(5):1085-8. doi: 10.1172/JCI109378.

DOI:10.1172/JCI109378
PMID:571874
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC372052/
Abstract

Peripheral blood lymphocytes from 38 patients with autoimmune thrombocytopenic purpura (AITP) were tested for HLA-A, -B, and -C alloantigens. Isolated B lymphocytes from 20 of these patients were tested for HLA-DRw (Ia) alloantigens. The profile of HLA alloantigens in the patients with AITP was significantly different from that of a matched control population. The most significant finding was the presence of the HLA-DRw2 alloantigen in 75% of patients as compared with 23% in the control population, P less than 0.001, relative risk 10.0 (A relative risk of 1 would indicate no association between the presence of the antigen and the disease.) The co-occurrence of either A3 and B7 (known to be in linkage disequilibrium with DRw2) or A26 and Bw38 was significantly increased as compared with the control population (P less than 0.001). Of the patients positive for DRw2, 47% had the association A26 and Bw38 as compared with the control population association incidence of 21% (P less than 0.1). Thus, in the patient population, A26-Bw38 appears to be a haplotype that is in linkage disequilibrium with DRw2 (as presumably is the case with A3-B7). These data indicate that a predisposition to AITP is inherited with a DRw2 gene of the major histocompatibility system.

摘要

对38例自身免疫性血小板减少性紫癜(AITP)患者的外周血淋巴细胞进行了HLA - A、- B和 - C同种抗原检测。对其中20例患者分离出的B淋巴细胞进行了HLA - DRw(Ia)同种抗原检测。AITP患者的HLA同种抗原谱与匹配的对照人群有显著差异。最显著的发现是,75%的患者存在HLA - DRw2同种抗原,而对照人群中这一比例为23%,P小于0.001,相对风险为10.0(相对风险为1表明抗原的存在与疾病之间无关联)。与对照人群相比,A3和B7(已知与DRw2处于连锁不平衡状态)或A26和Bw38的共出现显著增加(P小于0.001)。在DRw2阳性的患者中,47%具有A26和Bw38的关联,而对照人群的关联发生率为21%(P小于0.1)。因此,在患者群体中,A26 - Bw38似乎是一种与DRw2处于连锁不平衡状态的单倍型(推测A3 - B7也是如此)。这些数据表明,AITP的易感性是通过主要组织相容性系统的DRw2基因遗传的。

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Idiopathic thrombocytopenia, initial illness and long term follow up.特发性血小板减少症,初发病及长期随访
Arch Dis Child. 1984 Apr;59(4):316-22. doi: 10.1136/adc.59.4.316.
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Inherited predisposition to iridocyclitis with juvenile rheumatoid arthritis: selectivity among HLA-DR5 haplotypes.幼年类风湿关节炎伴发虹膜睫状体炎的遗传易感性:HLA - DR5单倍型之间的选择性
Proc Natl Acad Sci U S A. 1984 Jun;81(11):3539-42. doi: 10.1073/pnas.81.11.3539.

本文引用的文献

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Demonstration of a thrombocytopenic factor in the blood of patients with thrombocytopenic purpura.血小板减少性紫癜患者血液中血小板减少因子的证明。
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Mixed lymphocyte cultures in rheumatoid arthritis.类风湿关节炎中的混合淋巴细胞培养
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Platelet antibody in autoimmune thrombocytopenia.自身免疫性血小板减少症中的血小板抗体
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Chronic idiopathic thrombocytopenic purpura. A familial immunodeficiency syndrome?慢性特发性血小板减少性紫癜。一种家族性免疫缺陷综合征?
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Disease associations of the Ia-like human alloantigens. Contrasting patterns in rheumatoid arthritis and systemic lupus erythematosus.类Ia型人类同种异体抗原的疾病关联。类风湿性关节炎和系统性红斑狼疮中的对比模式。
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