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首页> 外文期刊>European journal of immunogenetics: official journal of the British Society for Histocompatibility and Immunogenetics >Sequence similarity matching: proposal of a structure-based rating system for bone marrow transplantation.
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Sequence similarity matching: proposal of a structure-based rating system for bone marrow transplantation.

机译:序列相似性匹配:提议基于结构的骨髓移植评估系统。

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摘要

Recent advances in DNA-based typing have led to the detection of a continuously growing number of HLA alleles. For this reason, HLA matching in transplantation of hematopoietic stem cells from unrelated donors has become increasingly complicated. When there is no genotypically identical sibling and there are several alternative potential donors that all have a mismatch at a relevant HLA locus, until now no rating system has existed indicating different levels of allogenicity. In order to find a theoretical approach to this problem we propose a rating system ('dissimilarity index') based on structural data of HLA class I molecules, and on published data about frequencies of naturally occurring amino acid exchanges. For demonstration we employ our rating system for the comparison of the HLA-A*23 and A*24 groups, both of which allelic products are subdivisions of the serological HLA-A9 family. Remarkable differences between the subtypes were revealed, which were superior to a simple sequence comparison. More surprisingly, it was uncovered that some alleles of the A*24 group showed fewer differences to A*2301 than to alleles within their own subtype group. Sequence similarity matching may serve as a starting point for the clinical evaluation of acceptable mismatches within the HLA-A9 family and serve as a model for other HLA class I groups.
机译:基于DNA的分型的最新进展已导致检测到数量不断增长的HLA等位基因。由于这个原因,从无关亲戚的造血干细胞移植中的HLA匹配变得越来越复杂。当没有基因型相同的同胞并且有几个备选的潜在供体在相关的HLA基因座上均不匹配时,直到现在还没有评级系统表明异源性水平不同。为了找到解决该问题的理论方法,我们提出了一种基于HLA I类分子的结构数据以及有关天然氨基酸交换频率的公开数据的评估系统(“相异指数”)。为了进行演示,我们使用了评级系统来比较HLA-A * 23和A * 24组,这两个等位基因产物都是血清学HLA-A9家族的细分。揭示了亚型之间的显着差异,其优于简单的序列比较。更令人惊讶的是,发现与A * 2301的亚型相比,与A * 2301的等位基因差异较小。序列相似性匹配可以作为临床评估HLA-A9家族中可接受的错配的起点,并且可以作为其他HLA I类组的模型。

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