Cariappa A, Sands B, Forcione D, Finkelstein D, Podolsky D K, Pillai S
Cancer Center, Massachusetts General Hospital, Boston, MA 02129, USA.
Gut. 1998 Aug;43(2):210-5. doi: 10.1136/gut.43.2.210.
Although inflammation in Crohn's disease is believed to be mediated by activated T cells, genotyping of all MHC class II alleles in white people with this disease has not been reported.
To perform a detailed molecular analysis of HLA DPB, DQB, and DRB genes in white patients with Crohn's disease and controls in order to determine if the inheritance of any class II genes confers susceptibility or resistance to this disease.
Complete molecular typing of HLA class II DPB, DQB, and DRB alleles was performed in 58 white patients with Crohn's disease and 93 healthy controls using a polymerase chain reaction-sequence specific oligonucleotide based approach.
No significant association with any DPB or DQB alleles was noted in patients with Crohn's disease. Since our previous studies had shown a strong association of an HLA DRB30301/DRB11302 haplotype with Crohn's disease, we re-examined this association using more stringent genotyping criteria. This haplotype was present in 20.7% of patients and 5.4% of controls (p = 0.0066; relative risk = 4.59).
The DRB30301/DRB11302 haplotype is the only significant MHC class II association noted in white people with Crohn's disease and represents the strongest association of any MHC or non-MHC locus with this disease.
尽管人们认为克罗恩病中的炎症是由活化的T细胞介导的,但尚未有关于该病白人患者所有MHC II类等位基因基因分型的报道。
对克罗恩病白人患者和对照者的HLA DPB、DQB和DRB基因进行详细的分子分析,以确定任何II类基因的遗传是否赋予对该病的易感性或抗性。
采用基于聚合酶链反应-序列特异性寡核苷酸的方法,对58例克罗恩病白人患者和93例健康对照者的HLA II类DPB、DQB和DRB等位基因进行完整的分子分型。
在克罗恩病患者中未发现与任何DPB或DQB等位基因有显著关联。由于我们之前的研究表明HLA DRB30301/DRB11302单倍型与克罗恩病有很强的关联,我们使用更严格的基因分型标准重新检查了这种关联。该单倍型在20.7%的患者和5.4%的对照者中存在(p = 0.0066;相对风险 = 4.59)。
DRB30301/DRB11302单倍型是在患有克罗恩病的白人中发现的唯一显著的MHC II类关联,并且代表了任何MHC或非MHC基因座与该病的最强关联。