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进行性系统性硬化症(硬皮病)中的人类白细胞抗原DR抗原

HLA-DR antigens in progressive systemic sclerosis (scleroderma).

作者信息

Whiteside T L, Medsger T A, Rodnan G P

出版信息

J Rheumatol. 1983 Feb;10(1):128-31.

PMID:6601709
Abstract

Typing at the HLA-DR locus was performed in 125 North American white patients with progressive systemic sclerosis (PSS). We could not confirm associations of PSS with the HLA-DR5 antigen or the HLA-B8/DR3 haplotype. A weak association of the DR1 antigen and PSS with diffuse scleroderma (27.5% vs 11.5% in local controls (corrected p less than 0.05) was observed. HLA-DR1 was significantly associated with the presence of anticentromere antibodies (p less than 0.05), and this combination was found more frequently in individuals with the CREST syndrome variant of PSS. This study failed to identify a clear-cut association between PSS and a genetic factor linked to the major histocompatibility complex.

摘要

对125例北美白人进行性系统性硬化症(PSS)患者进行了HLA - DR位点分型。我们无法证实PSS与HLA - DR5抗原或HLA - B8/DR3单倍型之间存在关联。观察到DR1抗原与PSS和弥漫性硬皮病之间存在微弱关联(局部对照中分别为27.5%和11.5%,校正p值小于0.05)。HLA - DR1与抗着丝点抗体的存在显著相关(p值小于0.05),并且这种组合在PSS的CREST综合征变体个体中更常见。本研究未能确定PSS与主要组织相容性复合体相关的遗传因素之间存在明确关联。

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