Toyoda H, Wang S J, Yang H Y, Redford A, Magalong D, Tyan D, McElree C K, Pressman S R, Shanahan F, Targan S R
Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, California.
Gastroenterology. 1993 Mar;104(3):741-8. doi: 10.1016/0016-5085(93)91009-7.
There are relatively few studies of HLA class II association either with Crohn's disease (CD) or ulcerative colitis (UC). The few available association studies have been carried out by serological techniques, and the results from these studies are inconclusive.
The association between HLA class II genes was studied using molecular genotyping in combination with allele-specific oligonucleotide hybridization by polymerase chain reactions.
In UC (n = 74), we observed a positive association with the HLA DR2 allele (P = 0.008) and negative associations with the DR4 (P = 0.018) and DRw6 (P = 0.028) when compared with ethnically matched controls (n = 77). No associations were observed with any DQ alleles. In contrast, in CD (n = 95) we observed a positive association with the combination of DR1 and DQw5 alleles (P = 0.021). Furthermore, stratifying DR1 and DQw5 alleles indicated that neither allele was independently associated with CD, suggesting that the association was with the haplotype rather than either of the alleles individually. A suballele of DQw5, DQB1*0501, contributed this haplotypic association (P = 0.012).
DR and DQ molecules firmly separate UC and CD on genetic grounds, suggesting that the contribution of the HLA class II genes to the disease susceptibility is quite different for the two disorders.
关于人类白细胞抗原(HLA)Ⅱ类分子与克罗恩病(CD)或溃疡性结肠炎(UC)相关性的研究相对较少。现有的少数相关性研究采用的是血清学技术,这些研究结果尚无定论。
采用分子基因分型结合聚合酶链反应的等位基因特异性寡核苷酸杂交技术,研究HLAⅡ类基因之间的相关性。
在溃疡性结肠炎患者(n = 74)中,与种族匹配的对照组(n = 77)相比,我们观察到与HLA DR2等位基因呈正相关(P = 0.008),与DR4(P = 0.018)和DRw6(P = 0.028)呈负相关。未观察到与任何DQ等位基因的相关性。相比之下,在克罗恩病患者(n = 95)中,我们观察到DR1和DQw5等位基因的组合呈正相关(P = 0.021)。此外,对DR1和DQw5等位基因进行分层分析表明,这两个等位基因均未单独与克罗恩病相关,这表明这种相关性与单倍型有关,而非单个等位基因。DQw5的一个亚等位基因DQB1*0501促成了这种单倍型相关性(P = 0.012)。
DR和DQ分子在遗传基础上明确区分了溃疡性结肠炎和克罗恩病,这表明HLAⅡ类基因对这两种疾病易感性的影响差异很大。