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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >The probability of HLA-C matching between patient and unrelated donor at the molecular level: estimations based on the linkage disequilibrium between DNA typed HLA-B and HLA-C alleles.
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The probability of HLA-C matching between patient and unrelated donor at the molecular level: estimations based on the linkage disequilibrium between DNA typed HLA-B and HLA-C alleles.

机译:患者和无关供体之间在分子水平上HLA-C匹配的可能性:基于DNA类型的HLA-B和HLA-C等位基因之间的连锁不平衡进行估算。

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摘要

BACKGROUND: Recent evidence suggests a more significant role of HLA-C as a target of alloreactions after bone marrow transplantation than previously suspected. Although linkage disequilibrium (LD) between HLA-B and -C serogroups is well documented, the level of LD at the allelic level is not known. In this study, we determine the LD between HLA-B and -C alleles and estimate the probability of molecular HLA-C matching between unrelated individuals who match for both HLA-B alleles. METHODS: The study included 727 haplotypes from 849 individuals who were HLA-A, -B, -C and -DRB1 typed by high-resolution PCR-SSOP technique. Zelterman's statistic was used to test for global LD between HLA loci. LD between specific HLA-B and -C allelic combinations was calculated from their observed and expected frequencies in the study haplotypes. The probability of HLA-C matching for specific HLA-B allele was estimated from contingency table generated from the HLA-B and -C haplotypes. RESULTS: HLA-C was found to exist in LD with HLA-A and -B, as well as -DRB1, loci; however, it was strongest between HLA-B and -C loci. A marked variability in the level of LD between specific HLA-B and -C alleles was noticed. A strong LD was seen in some allele pairs like B*0702-C*w0702, B*3501-Cw*0401, and B*0801-Cw*0701. The overall estimated probability of HLA-C matching between unrelated individuals that match for both HLA-B alleles is 42.25%. For 237 (72.9%) of 325 combinations involving the 25 commonest HLA-B alleles, the estimated probability that the HLA-B-matched unrelated individuals will match for both HLA-C alleles is less than 50%. In addition, a 100% probability of matching for both HLA-C alleles is expected only if both individuals bear either B*0801/ B*0801 or B*4901/B*4901 or B*0801/B*4901. Probability tables for common alleles are presented. CONCLUSIONS: We conclude that, despite matching for both HLA-B alleles by high resolution DNA typing and the presence of a strong LD between HLA-B and HLA-C loci, unrelated individuals are more likely to mismatch rather than match for one or both HLA-C alleles.
机译:背景:最近的证据表明,HLA-C作为骨髓移植后的同种异体反应的靶标,其作用要比先前怀疑的更为重要。尽管HLA-B和-C血清群之间的连锁不平衡(LD)有充分的文献证明,但等位基因水平的LD水平尚不清楚。在这项研究中,我们确定了HLA-B和-C等位基因之间的LD,并估计了两个HLA-B等位基因都匹配的不相关个体之间分子HLA-C匹配的可能性。方法:该研究包括来自849个个体的727个单倍型,这些个体是通过高分辨率PCR-SSOP技术分型的HLA-A,-B,-C和-DRB1。 Zelterman的统计数据用于测试HLA位点之间的全局LD。根据研究单倍型中它们的观察频率和预期频率,计算特定HLA-B和-C等位基因组合之间的LD。根据从HLA-B和-C单倍型产生的列联表估计特定HLA-B等位基因的HLA-C匹配概率。结果:发现LDA中存在HLA-C和HLA-A和-B,以及-DRB1基因座。但是,它在HLA-B和-C基因座之间最强。注意到在特定的HLA-B和-C等位基因之间LD水平的显着变化。在一些等位基因对中,例如B * 0702-C * w0702,B * 3501-Cw * 0401和B * 0801-Cw * 0701,观察到强LD。在两个HLA-B等位基因均匹配的不相关个体之间,HLA-C匹配的总体估计概率为42.25%。对于涉及25个最常见的HLA-B等位基因的325种组合中的237种(72.9%),与HLA-B匹配的无关个体将同时匹配两个HLA-C等位基因的估计概率小于50%。另外,仅当两个人都携带B * 0801 / B * 0801或B * 4901 / B * 4901或B * 0801 / B * 4901时,才预期两个HLA-C等位基因都匹配的100%概率。列出了常见等位基因的概率表。结论:我们得出结论,尽管通过高分辨率DNA分型匹配了两种HLA-B等位基因,并且在HLA-B和HLA-C基因座之间存在强LD,但不相关的个​​体更可能错配而不是匹配其中一个或两个HLA-C等位基因。

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