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成人和青少年类风湿性关节炎中不同的人类白细胞抗原-D关联。

Different HLA-D associations in adult and juvenile rheumatoid arthritis.

作者信息

Stastny P, Fink C W

出版信息

J Clin Invest. 1979 Jan;63(1):124-30. doi: 10.1172/JCI109265.

Abstract

HLA-D typing was performed in 126 patients with juvenile rheumatoid arthritis. HLA-DW4, the antigen found in previous studies to characterize adult rheumatoid arthritis, had a significantly lower frequency in children with arthritis than in normal controls (P less than 0.04). By contrast, in children the antigens HLA-DW7 (P less than 0.03) and HLA-DW8 (P less than 0.01) were increased compared to controls. The antigen TMo, detected with homozygous typing cells from a child with juvenile rheumatoid arthritis, was found to be related to the cross-reactive specificities HLA-DW7 and DW11. 46% of the patients with persistent pauciarticular arthritis of childhood typed for the antigen TMo, compared to only 1% of normal controls. Thus the relative risk for persistent pauciarticular arthritis in relation to the presence of TMo was 67.7 (P less than 0.0001). These results provide evidence of fundamental differences between adult rheumatoid arthritis and arthritis of childhood. The latter group appears to include a population distinguishable clinically and characterized in these studies by the HLA-D determinant TMo.

摘要

对126例青少年类风湿性关节炎患者进行了HLA - D分型。先前研究发现可作为成人类风湿性关节炎特征的抗原HLA - DW4,在患有关节炎的儿童中的出现频率显著低于正常对照组(P小于0.04)。相比之下,与对照组相比,儿童中抗原HLA - DW7(P小于0.03)和HLA - DW8(P小于0.01)的出现频率有所增加。用一名青少年类风湿性关节炎患儿的纯合分型细胞检测到的抗原TMo,被发现与交叉反应特异性HLA - DW7和DW11有关。46%的儿童持续性少关节性关节炎患者检测出抗原TMo,而正常对照组仅为1%。因此,与TMo的存在相关的持续性少关节性关节炎的相对风险为67.7(P小于0.0001)。这些结果证明了成人类风湿性关节炎与儿童关节炎之间存在根本差异。后一组似乎包括一个在临床上可区分的人群,在这些研究中其特征为HLA - D决定簇TMo。

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本文引用的文献

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On estimating the relation between blood group and disease.关于评估血型与疾病之间的关系。
Ann Hum Genet. 1955 Jun;19(4):251-3. doi: 10.1111/j.1469-1809.1955.tb01348.x.
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HL-A, immune-response genes, and disease.人类白细胞抗原、免疫反应基因与疾病
Lancet. 1974 Jun 22;1(7869):1269-75. doi: 10.1016/s0140-6736(74)90021-x.
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Cellular distrubtion, purification, and molecular nature of human Ia antigens.
Scand J Immunol. 1977;6(5):439-52. doi: 10.1111/j.1365-3083.1977.tb02101.x.

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