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北爱尔兰人群中HLA-DPB1等位基因的频率,包括一种新的DPB1序列。

Frequency of HLA-DPB1 alleles, including a novel DPB1 sequence, in the Northern Ireland population.

作者信息

Savage D A, Middleton D, Trainor F, Taylor A, McKenna P G, Darke C

机构信息

Northern Ireland Tissue Typing Service, Belfast City Hospital.

出版信息

Hum Immunol. 1992 Apr;33(4):235-42. doi: 10.1016/0198-8859(92)90330-p.

Abstract

HLA-DPB1 allele frequencies in 150 unrelated normal individuals from Northern Ireland were determined using oligonucleotide typing methods. HLA-DPB10401 was the most common allele in the population possessed by 75.3% of subjects, followed by DPB10201 (20.7%). In addition to these alleles, only HLA-DPB10402, -DPB10301, and -DPB10501 were present in subjects at frequencies greater than 10%. The results in this study are in broad agreement with other Caucasoid studies, but there is regional and ethnic variation in HLA-DP allele frequencies. Three DPB1 alleles were found to be in linkage disequilibrium with HLA-DR antigens determined by RFLP, namely, DPB10101 with DRw17 (Dw24 associated) RFLP, DPB10501 with DRw13-Dw19 RFLP, and DPB11901 with DRw13-Dw18 (Dw25 associated) RFLP. One individual revealed a novel DPB1 pattern of probe reactivity, which following DNA sequencing was found to be HLA-DPB1*2001. To assess the system used and to compare consistency of results between laboratories, 62 cell lines were oligotyped for HLA-DP. The results revealed the system described here to be extremely accurate and showed excellent agreement of HLA-DP typing results for cell lines between laboratories.

摘要

采用寡核苷酸分型方法测定了150名来自北爱尔兰的无关正常个体的HLA - DPB1等位基因频率。HLA - DPB10401是该人群中最常见的等位基因,75.3%的个体拥有该基因,其次是DPB10201(20.7%)。除了这些等位基因外,只有HLA - DPB10402、- DPB10301和- DPB10501在个体中的频率大于10%。本研究结果与其他高加索人群研究大致相符,但HLA - DP等位基因频率存在区域和种族差异。发现三个DPB1等位基因与通过限制性片段长度多态性(RFLP)测定的HLA - DR抗原处于连锁不平衡状态,即DPB10101与DRw17(与Dw24相关)RFLP、DPB10501与DRw13 - Dw19 RFLP以及DPB11901与DRw13 - Dw18(与Dw25相关)RFLP。一名个体显示出一种新的探针反应性DPB1模式,经DNA测序后发现是HLA - DPB1*2001。为了评估所使用的系统并比较各实验室结果的一致性,对62个细胞系进行了HLA - DP寡核苷酸分型。结果表明,此处描述的系统极其准确,各实验室对细胞系的HLA - DP分型结果显示出极好的一致性。

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