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早发性少关节型幼年慢性关节炎中的易感和保护性主要组织相容性复合体II类等位基因

Susceptible and protective major histocompatibility complex class II alleles in early-onset pauciarticular juvenile chronic arthritis.

作者信息

Haas J P, Nevinny-Stickel C, Schoenwald U, Truckenbrodt H, Suschke J, Albert E D

机构信息

Immunogenetics Laboratory Children's LMU Polyclinic, Munich, Germany.

出版信息

Hum Immunol. 1994 Nov;41(3):225-33. doi: 10.1016/0198-8859(94)90040-x.

Abstract

Oligonucleotide typing for alleles of the MHC loci DRB1, DQA1, and DQB1 was performed in 160 patients suffering from EOPA, JCA (or JRA = juvenile rheumatoid arthritis). Allele and haplotype frequencies of the patients were compared with the data of an unrelated healthy control group consisting of 200 individuals. Analysis of frequencies shows that HLA alleles are associated not only with susceptibility to EOPA-JCA but also with protection from the disease. The presence of protection connected with certain HLA alleles was assessed using a calculation which takes into account the condition that if one allele is increased, all other alleles of the same locus must be decreased in compensation. Protection can be assumed only in cases where a given allele has an observed frequency which is significantly beyond the expected compensatory decrease. Thus a hierarchy of associations was observed in EOPA-JCA patients. The alleles of the haplotypes DRB111 (12)-DQA10501-DQB10301 as well as DRB108-DQA10401-DQB10402 were found to be associated with susceptibility to disease, whereas the alleles DRB107 and DQA10201 converge with significant protection from the disease. Whereas the association with disease susceptibility seems to depend on a sequence motif encoded in certain DQA1 alleles, protection is associated either with alleles of DRB1 or DQA1.

摘要

对160例患有侵蚀性多关节型幼年特发性关节炎(EOPA)、幼年特发性关节炎(JCA,或幼年类风湿性关节炎JRA)的患者进行了主要组织相容性复合体(MHC)基因座DRB1、DQA1和DQB1等位基因的寡核苷酸分型。将患者的等位基因和单倍型频率与由200名个体组成的无关健康对照组的数据进行比较。频率分析表明,人类白细胞抗原(HLA)等位基因不仅与EOPA-JCA易感性相关,还与对该疾病的保护作用相关。使用一种计算方法评估了与某些HLA等位基因相关的保护作用,该计算方法考虑到如果一个等位基因增加,同一基因座的所有其他等位基因必须相应减少以作补偿这一条件。只有在给定等位基因的观察频率明显超出预期补偿性减少的情况下,才能假定存在保护作用。因此,在EOPA-JCA患者中观察到了一种关联层次结构。发现单倍型DRB111(12)-DQA10501-DQB10301以及DRB108-DQA10401-DQB10402的等位基因与疾病易感性相关,而等位基因DRB107和DQA10201则与对疾病的显著保护作用相关。与疾病易感性的关联似乎取决于某些DQA1等位基因中编码的序列基序,而保护作用则与DRB1或DQA1的等位基因相关。

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