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一个有多例类风湿关节炎患者的家族中的人类白细胞抗原单倍型

HLA haplotypes in a family with multiple cases of rheumatoid arthritis.

作者信息

Michalski J P, McCombs C C, DeJesus I B, Anderson J L

出版信息

J Rheumatol. 1982 May-Jun;9(3):451-4.

PMID:6214630
Abstract

Population studies have identified the histocompatibility antigen HLA-DR4 to be a genetic marker of significantly increased risk for the development of rheumatoid arthritis (RA). Family studies are now beginning to elucidate the role of this and other genetic factors in the pathogenesis of RA. We have studied a large family in which the mother and 3 of the 6 children have seropositive RA. One maternal and 1 paternal HLA haplotype contain HLA-DR4. The mother and the 2 children with the maternal DR4 containing haplotype have RA. One sibling inherited neither of the DR4 haplotypes, yet developed RA at age 20. The inheritance of RA in this family illustrates the complexity of the genetic predisposition to this immunologically mediated disorder.

摘要

人群研究已确定组织相容性抗原HLA - DR4是类风湿性关节炎(RA)发病风险显著增加的遗传标志物。家族研究如今开始阐明该遗传因素及其他遗传因素在RA发病机制中的作用。我们研究了一个大家庭,其中母亲以及6个孩子中的3个患有血清阳性RA。一条母系和一条父系HLA单倍型含有HLA - DR4。母亲以及携带母系含DR4单倍型的2个孩子患有RA。一个兄弟姐妹既未继承任何一种DR4单倍型,但在20岁时患上了RA。这个家族中RA的遗传情况说明了这种免疫介导疾病遗传易感性的复杂性。

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