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患有因子 VIII 抗体的血友病患者的组织相容性抗原模式。

Histocompatibility antigen patterns in haemophilic patients with factor VIII antibodies.

作者信息

Aly A M, Aledort L M, Lee T D, Hoyer L W

机构信息

Holland Laboratory, American Red Cross Blood Services, Rockville, MD 20855.

出版信息

Br J Haematol. 1990 Oct;76(2):238-41. doi: 10.1111/j.1365-2141.1990.tb07878.x.

Abstract

A number of studies suggest that there is a genetic basis for the formation by some haemophilia A patients of antibodies that inactivate factor VIII. In our study, human leucocyte antigen (HLA)-A, B, C, DR and DQ typing was carried out for 44 haemophilia A patients, including 16 who had developed an antibody to factor VIII. In contrast to previous reports, we found no association between HLA-DR antigens and haemophilia A per se or the formation of a factor VIII inhibitor. However, there was an absence of HLA-Cw5 in the 16 haemophilic patients who had formed an antibody to factor VIII. This finding, consistent with a previous report, identified a statistically significant difference in HLA-Cw5 frequency when the inhibitor patient group was compared to multi-transfused haemophilic patients who had no inhibitor (11/28).

摘要

多项研究表明,部分甲型血友病患者体内产生使凝血因子VIII失活的抗体存在遗传基础。在我们的研究中,对44例甲型血友病患者进行了人类白细胞抗原(HLA)-A、B、C、DR和DQ分型,其中16例已产生针对凝血因子VIII的抗体。与之前的报道不同,我们发现HLA-DR抗原与甲型血友病本身或凝血因子VIII抑制剂的形成之间无关联。然而,在已产生针对凝血因子VIII抗体的16例血友病患者中不存在HLA-Cw5。这一发现与之前的一份报告一致,在将产生抑制剂的患者组与未产生抑制剂的多次输血血友病患者(11/28)进行比较时,发现HLA-Cw5频率存在统计学上的显著差异。

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