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与HLA扩展单倍型及C2缺陷相关的HLA - Cw等位基因。

HLA-Cw alleles associated with HLA extended haplotypes and C2 deficiency.

作者信息

Clavijo O P, Delgado J C, Awdeh Z L, Fici D, Turbay D, Alper C A, Truedsson L, Yunis E J

机构信息

Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

出版信息

Tissue Antigens. 1998 Sep;52(3):282-5. doi: 10.1111/j.1399-0039.1998.tb03045.x.

Abstract

There are four MHC-linked complement genes, BF, C2, C4A and C4B, that are inherited as single DNA units, known as complotypes. Extended haplotypes were initially defined by studying the distribution of complotypes in relation to HLA-B and HLA-DR loci in Caucasian families. In order to analyze the distribution of HLA-Cw alleles in relation to extended haplotypes, we studied a large panel of MHC homozygous and heterozygous cell lines representing previously described Caucasian-derived extended haplotypes and 14 patients with complete C2 deficiency. HLA alleles were assigned using sequence-specific oligonucleotide probe hybridization (SSOP). Family analysis served to assign haplotypes for heterozygous samples. We found distinctive HLA-Cw alleles for each independent extended haplotype. Their association in each instance was statistically significant. All patients with C2 deficiency carrying the haplotype [HLA-B18, S042, DR2] were associated with HLA-Cw*1203. These conserved allelic combinations may become an important tool for the study of human evolution and may contribute to the expeditious selection of prospective donors in clinical transplantation.

摘要

有四个与MHC连锁的补体基因,即BF、C2、C4A和C4B,它们作为单个DNA单位遗传,称为补体型。最初通过研究白种人家庭中补体型与HLA - B和HLA - DR位点的分布关系来定义扩展单倍型。为了分析HLA - Cw等位基因与扩展单倍型的分布关系,我们研究了一大组代表先前描述的源自白种人的扩展单倍型的MHC纯合和杂合细胞系以及14例C2完全缺乏的患者。使用序列特异性寡核苷酸探针杂交(SSOP)来确定HLA等位基因。家系分析用于确定杂合样本的单倍型。我们发现每个独立的扩展单倍型都有独特的HLA - Cw等位基因。它们在每种情况下的关联都具有统计学意义。所有携带单倍型[HLA - B18,S042,DR2]的C2缺乏患者都与HLA - Cw*1203相关。这些保守的等位基因组合可能成为人类进化研究的重要工具,并可能有助于临床移植中快速选择潜在供体。

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