Machens A, Löliger C, Pichlmeier U, Emskötter T, Busch C, Izbicki J R
Department of Surgery, University of Hamburg, Germany.
Clin Immunol. 1999 Jun;91(3):296-301. doi: 10.1006/clim.1999.4710.
The aim of this study was to investigate associations between thymic pathology and HLA in myasthenia gravis. HLA typing was performed in 95 of 125 Caucasian patients who underwent transsternal thymectomy for myasthenia gravis between 1976 and 1995. Multiple comparison procedures applied within each HLA locus demonstrated significant correlations between the ancestral suprahaplotype A1 B8 DRB10301 DRB30101 DQA1*0501 and thymic hyperplasia and between HLA-A24 and thymoma. A weaker association was found between A3 and thymic atrophy and thymolipoma. On logistic discriminant analysis, HLA-B8 (P = 0.001) and HLA-A3 (P = 0.028) were identified as the only significant classifiers to jointly provide a good discriminator between the thymic pathologies. When the suitability of HLA for detection of thymoma was examined in a second logistic regression analysis, both HLA-A24 (OR 9.7; 95% CI [1.6, 73.7]) and HLA-B8 (OR 0.1; 95% CI [0.0, 0.5]) were significant predictive factors. The above correlations between thymic pathology and HLA-A3, HLA-A24, and HLA-B8 (but not MHC class II alleles) suggest an involvement of MHC class I restricted T cells in myasthenic autoimmunity that may partially be reflected by thymic pathology.
本研究的目的是调查重症肌无力患者胸腺病理与人类白细胞抗原(HLA)之间的关联。对1976年至1995年间因重症肌无力接受经胸骨胸腺切除术的125例白种人患者中的95例进行了HLA分型。在每个HLA位点内应用多重比较程序,结果显示祖传超单倍型A1 B8 DRB10301 DRB30101 DQA1*0501与胸腺增生之间以及HLA - A24与胸腺瘤之间存在显著相关性。发现A3与胸腺萎缩和胸腺脂肪瘤之间的关联较弱。在逻辑判别分析中,HLA - B8(P = 0.001)和HLA - A3(P = 0.028)被确定为仅有的显著分类器,它们共同为胸腺病理之间提供了良好的判别能力。在第二次逻辑回归分析中检查HLA用于检测胸腺瘤的适用性时,HLA - A24(比值比9.7;95%可信区间[1.6, 73.7])和HLA - B8(比值比0.1;95%可信区间[0.0, 0.5])均为显著的预测因素。胸腺病理与HLA - A3、HLA - A24和HLA - B8(而非MHC II类等位基因)之间的上述相关性表明,MHC I类限制性T细胞参与了重症肌无力自身免疫,这可能部分由胸腺病理反映出来。