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恶性贫血及内因子抗体与人类白细胞抗原-D的关联。

Association of pernicious anemia and intrinsic factor antibody with HLA-D.

作者信息

Thomsen M, Jørgensen F, Brandsborg M, Gimsing P, Nielsen J L, Ryder L P, Svejgaard A

出版信息

Tissue Antigens. 1981 Jan;17(1):97-103. doi: 10.1111/j.1399-0039.1981.tb00672.x.

Abstract

One-hundred-and-six patients with pernicious anemia were HLA-A, B, C typed by serological technique and HLA-D typed by mixed lymphocyte culture technique for the specificities HLA-Dw1 - 8 and the locally defined D "H". In 13 cases, the D-typing was unsuccessful due to technical difficulties. HLA-A, B, C antigen frequencies did not show any significant deviation from expected values, while D typing showed increased frequencies of Dw2 and Dw5 and a possibly decreased frequency of Dw3. The typing was compared with clinical data such as the presence of organ specific autoimmune disease in first degree relatives, presence of anemia or myelopathy at time of diagnosis and presence of antibodies towards parietal cells or intrinsic factor. The presence of intrinsic factor antibody was associated with the presence of Dw2 and a decrease of Dw5 and possibly also with a decrease of Dw4. No associations were found for the other investigated parameters. If intrinsic factor antibodies have a pathogenetic role, our findings might reflect a heterogeneity of pernicious anemia. These findings and the recently reported association between HLA-DR5 and Hashimoto's disease link these two thyrogastric diseases together to form a special subgroup within the group of organspecific autoimmune diseases; the other diseases in the group have as a common denominator the frequent presence of D/DR3.

摘要

采用血清学技术对106例恶性贫血患者进行HLA - A、B、C分型,采用混合淋巴细胞培养技术对HLA - Dw1 - 8及本地定义的D“H”特异性进行HLA - D分型。13例因技术困难D分型未成功。HLA - A、B、C抗原频率与预期值无显著偏差,而D分型显示Dw2和Dw5频率增加,Dw3频率可能降低。将该分型结果与临床数据进行比较,如一级亲属中器官特异性自身免疫性疾病的存在情况、诊断时贫血或脊髓病的存在情况以及壁细胞或内因子抗体的存在情况。内因子抗体的存在与Dw2的存在以及Dw5的减少有关,也可能与Dw4的减少有关。其他研究参数未发现相关性。如果内因子抗体具有致病作用,我们的发现可能反映了恶性贫血的异质性。这些发现以及最近报道的HLA - DR5与桥本氏病之间的关联将这两种甲状腺和胃部疾病联系在一起,在器官特异性自身免疫性疾病组中形成一个特殊的亚组;该组中的其他疾病的一个共同特征是频繁出现D/DR3。

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