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HLA基因型分析与胰岛素依赖型糖尿病易感性:与HLA-DP端粒的关联图谱

Analysis of HLA genotypes and susceptibility to insulin-dependent diabetes mellitus: association maps telomeric to HLA-DP.

作者信息

Baisch J M, Capra J D

机构信息

Center for Diabetes Research, University of Texas Southwestern Medical Center, Dallas 75235-9048.

出版信息

Scand J Immunol. 1992 Aug;36(2):331-40. doi: 10.1111/j.1365-3083.1992.tb03106.x.

Abstract

There is convincing evidence that certain combinations of alleles within the human leucocyte antigen (HLA) complex, particularly within HLA-DQ, are associated with either resistance or susceptibility to insulin-dependent diabetes mellitus (IDDM). A previous study conducted on a large, well-defined group of patients demonstrated that DQB10302 (DQw8) conferred 'dominant susceptibility' to IDDM while DQB10602 (DQw1.2) conferred 'dominant protection'. The availability of this population enabled us to further assess susceptibility associated with other class II alleles in an effort to map an outside HLA boundary of disease association. Using a group-specific polymerase chain reaction protocol and a series of oligonucleotide probes which define over twenty DP beta alleles, we studied 286 unrelated Caucasian patients with IDDM and 184 normal subjects. We found that while several alleles are increased (DPB10201, DPB10301, DPB10402) or decreased (DPB10101, DPB1*0202) in the diabetic population compared with the normal subjects, the HLA association with IDDM is considerably weaker at the DP locus. These data define the centromeric boundary for the HLA-associated susceptibility gene in IDDM, localizing susceptibility to the region telomeric to HLA-DP up to and including HLA-DQ.

摘要

有确凿证据表明,人类白细胞抗原(HLA)复合体中的某些等位基因组合,尤其是HLA - DQ内的组合,与胰岛素依赖型糖尿病(IDDM)的抗性或易感性相关。先前对一大组明确界定的患者进行的一项研究表明,DQB10302(DQw8)赋予IDDM“显性易感性”,而DQB10602(DQw1.2)赋予“显性保护”。这一人群的存在使我们能够进一步评估与其他II类等位基因相关的易感性,以便绘制疾病关联的HLA外部边界。我们使用组特异性聚合酶链反应方案和一系列可定义二十多种DPβ等位基因的寡核苷酸探针,研究了286名无亲缘关系的白种人IDDM患者和184名正常受试者。我们发现,与正常受试者相比,糖尿病患者群体中几个等位基因增加(DPB10201、DPB10301、DPB10402)或减少(DPB10101、DPB1*0202),但在DP位点,HLA与IDDM的关联要弱得多。这些数据确定了IDDM中HLA相关易感性基因的着丝粒边界,将易感性定位到HLA - DP端粒区域直至并包括HLA - DQ。

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