Haas J P, Truckenbrodt H, Paul C, Hoza J, Scholz S, Albert E D
Universitatskinderklinik, Erlangen, Germany.
Clin Exp Rheumatol. 1994 Sep-Oct;12 Suppl 10:S7-14.
A set of 200 patients with early onset pauciarticular juvenile chronic arthritis (EOPA-JCA) from Munich (165) and Prague (35) was investigated for the subtypes of HLA-DRB1*03, *08, 11, 12, 13 and 14. In addition, the relationship of DRB1, DQA1, DQB1 and DPB1 alleles with iridocyclitis in patients with EOPA-JCA was investigated. Subtyping for DRB103 was not informative, as all DR3 positive patients and all except one of the controls possessed DRB10301. Thus, the role of DRB10302 could not be assessed. The subtypes for DRB112, 13, and 14 did not reveal any statistically significant difference between patients and controls. In contrast, the subtype DRB11104 was the one most strongly associated with EOPA-JCA (chi 2 31.2, p value < 10(-6)). It appears that the subtype DRB11103 may also be associated with EOPA-JCA. The association of EOPA-JCA with DR8 is almost exclusively due to the subtype *0801. For the other alleles *0802, 0803, and 0804 there is no evidence for or against involvement in JCA. The analysis of iridocyclitis in EOPA-JCA revealed that DRB11104 is not more frequent in patients with eye disease than in patients without eye disease. The presence of DRB101 appears to convey some protective effect against the occurrence of iridiocylitis in EOPA-JCA, as had been previously observed by Melin-Aldana et al.
对来自慕尼黑(165例)和布拉格(35例)的200例早发型少关节型幼年慢性关节炎(EOPA-JCA)患者进行了HLA-DRB103、08、11、12、13和14亚型的研究。此外,还研究了EOPA-JCA患者中DRB1、DQA1、DQB1和DPB1等位基因与虹膜睫状体炎的关系。对DRB103进行亚型分析无意义,因为所有DR3阳性患者以及除1例对照外的所有对照均携带DRB10301。因此,无法评估DRB10302的作用。DRB112、13和14的亚型在患者和对照之间未显示出任何统计学上的显著差异。相比之下,DRB11104亚型与EOPA-JCA的关联最为强烈(卡方值31.2,p值<10(-6))。似乎DRB11103亚型也可能与EOPA-JCA相关。EOPA-JCA与DR8的关联几乎完全归因于0801亚型。对于其他等位基因0802、0803和0804,没有证据表明其与幼年慢性关节炎有关或无关。对EOPA-JCA患者虹膜睫状体炎的分析显示,患眼疾的患者中DRB11104的频率并不高于未患眼疾的患者。正如Melin-Aldana等人之前所观察到的,DRB101的存在似乎对EOPA-JCA患者虹膜睫状体炎的发生具有一定的保护作用。