Chuang L M, Jou T S, Wu H P, Chang H M, Tsai W Y, Hsieh R P, Chen K H, Lin B J, Tai T Y
Department of Internal Medicine, College of Medicine, National Taiwan University, Taipei, Republic of China.
Proc Natl Sci Counc Repub China B. 1995 Apr;19(2):73-9.
To study the role of the HLA DQA1 gene and its interaction with DQB1 in the susceptibility of IDDM, subjects with insulin-dependent (type 1) diabetes mellitus and non-diabetic unrelated controls were recruited from a Chinese population living in northern Taiwan. HLA DQA1 exon 2 was enzymatically amplified by polymerase chain reaction. HLA DQA1 alleles were diagnosed by dot blotting and hybridization with 11 sequence-specific oligonucleotide probes. Among all the DQA1 alleles, DQA10301 and DQA10501 were more frequent while DQA10102, DQA10103 and DQA10601 were less frequent in Chinese with IDDM than in controls. Among the DQA1 genotypes, only DQA10301/0301 and DQA10301/0501 were associated with increased risk to IDDM while DQA10301/0601 and DQA1*0102/0103 were protective against IDDM in our population. As the cell surface HLA DQ molecules were formed from each DQA1 and DQB1 alleles either in cis- or trans-position, the numbers of susceptible HLA DQ alpha beta heterodimers were then derived from the genotypes of HLA DQA1/DQB1 in each person. The numbers of the possible diabetogenic DQ alpha beta dimers correlated with the degree of risk to IDDM (r = 0.92) but were not statistically significant (p > 0.05). Subjects with absence of diabetogenic HLA DQ molecules were resistant to developing IDDM while subjects with two or more forms of diabetogenic DQ molecules were associated with increased risk to IDDM. In conclusion, both DQA1 and DQB1 genes, which determine the formation of susceptible DQ alpha beta heterodimers, were significantly associated with IDDM in Chinese subjects living in Taiwan.
为研究HLA DQA1基因及其与DQB1的相互作用在胰岛素依赖型糖尿病(IDDM)易感性中的作用,从居住在台湾北部的中国人群中招募了胰岛素依赖型(1型)糖尿病患者和非糖尿病无关对照。通过聚合酶链反应酶促扩增HLA DQA1外显子2。通过斑点印迹法并用11种序列特异性寡核苷酸探针杂交来诊断HLA DQA1等位基因。在所有DQA1等位基因中,DQA10301和DQA10501在中国IDDM患者中比在对照中更常见,而DQA10102、DQA10103和DQA10601则较少见。在DQA1基因型中,只有DQA10301/0301和DQA10301/0501与IDDM风险增加相关,而DQA10301/0601和DQA1*0102/0103在我们的人群中对IDDM有保护作用。由于细胞表面HLA DQ分子由每个顺式或反式位置的DQA1和DQB1等位基因形成,因此易感HLA DQαβ异二聚体的数量随后从每个人的HLA DQA1/DQB1基因型中得出。可能的致糖尿病性DQαβ二聚体的数量与IDDM风险程度相关(r = 0.92),但无统计学意义(p>0.05)。缺乏致糖尿病性HLA DQ分子的受试者对发生IDDM有抵抗力,而具有两种或更多种致糖尿病性DQ分子形式的受试者与IDDM风险增加相关。总之,决定易感DQαβ异二聚体形成的DQA1和DQB1基因均与居住在台湾的中国受试者的IDDM显著相关。