Mantovani V, Corazza G R, Angelini G, Delfino L, Frisoni M, Mirri P, Valentini R A, Barboni P, Gasbarrini G, Ferrara G B
Tissue Typing Laboratory, Malpighi Hospital, Bologna, Italy.
Clin Exp Immunol. 1991 Jan;83(1):74-8. doi: 10.1111/j.1365-2249.1991.tb05591.x.
Susceptibility to coeliac disease is strongly associated with some HLA class II antigens, encoded by the HLA-D region. Since the HLA-DQ locus seems to be primarily involved, we have analysed by polymerase chain reaction amplification and allele-specific oligonucleotide hybridization the most polymorphic region of the HLA-DQ A1 gene. No difference was observed between the 20 coeliac patients and 20 HLA-D-matched healthy controls who took part in the study. Furthermore, in patients and controls, the restriction fragment length polymorphism analysis of the HLA-DQ A gene using the restriction enzyme BglII did not disclose any specific disease-associated fragment. Our results are not consistent with a unique DQ A coeliac disease-associated sequence, but rather with the hypothesis that some polymorphic residues or allelic hypervariable regions, although found also in the normal population, can predispose to coeliac disease due to their higher frequency in this condition.
腹腔疾病易感性与某些由HLA - D区域编码的HLA II类抗原密切相关。由于HLA - DQ基因座似乎起主要作用,我们通过聚合酶链反应扩增和等位基因特异性寡核苷酸杂交分析了HLA - DQ A1基因的最具多态性区域。参与研究的20名腹腔疾病患者和20名HLA - D匹配的健康对照之间未观察到差异。此外,在患者和对照中,使用限制性内切酶BglII对HLA - DQ A基因进行的限制性片段长度多态性分析未发现任何与疾病相关的特异性片段。我们的结果与单一的DQ A腹腔疾病相关序列不一致,而是与以下假设相符:某些多态性残基或等位基因高变区,尽管在正常人群中也有发现,但由于在这种疾病中出现频率较高,可能会使人易患腹腔疾病。