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一种分析人类白细胞抗原(HLA)Ⅱ类多态性的新方法:“HLA寡核苷酸分型”

A new approach for the analysis of HLA class II polymorphism: 'HLA oligotyping'.

作者信息

Tiercy J M, Jeannet M, Mach B

机构信息

Transplantation Immunology Unit, Hôpital Cantonal Universitaire de Genève, Switzerland.

出版信息

Blood Rev. 1990 Mar;4(1):9-15. doi: 10.1016/0268-960x(90)90012-h.

Abstract

Histocompatibility typing allows the matching of patients and donors in organ transplantation, and the accuracy of HLA matching influences to a great extent the clinical outcome. Recent breakthroughs in the molecular biology of HLA class II genes have revealed that the degree of HLA diversity and polymorphism is in fact much greater than was expected on the basis of the traditional serological HLA typing assays. In parallel, it has become possible to analyse this extensive polymorphism directly at the level of the HLA class II genes and of their DNA sequences. We have described a DNA typing procedure referred to as 'HLA oligotyping' which is based on the hybridisation of allele and loci specific oligonucleotide probes. This procedure has now become operational on a large scale and this review describes the principles and major applications of the technique. It consists in the hybridisation of DNA with informative sequence-specific oligonucleotide probes, following an amplification of DNA in vitro by the polymerase chain reaction (PCR). The use of this highly sensitive technique for HLA-DR, -DQ and -DP typing is discussed, focusing on the clinical applications in the field of organ transplantation, particularly for bone marrow transplantation with unrelated donors. It now allows the unambiguous identification of all HLA subtypes, including those that cannot be recognised otherwise, and it represents powerful complement to current methods of HLA typing. Finally this methodology is widely used in HLA-disease association studies, aiming at the characterisation of HLA class II epitopes involved in the susceptibility or resistance to autoimmune diseases.

摘要

组织相容性分型可实现器官移植中患者与供体的匹配,而HLA匹配的准确性在很大程度上影响临床结果。HLA II类基因分子生物学的最新突破表明,HLA的多样性和多态性程度实际上比基于传统血清学HLA分型检测所预期的要高得多。与此同时,直接在HLA II类基因及其DNA序列水平分析这种广泛的多态性已成为可能。我们描述了一种称为“ HLA寡核苷酸分型”的DNA分型方法,该方法基于等位基因和基因座特异性寡核苷酸探针的杂交。此方法现已大规模投入使用,本综述描述了该技术的原理和主要应用。它包括在通过聚合酶链反应(PCR)体外扩增DNA之后,使DNA与信息性序列特异性寡核苷酸探针杂交。本文讨论了这种高灵敏度技术在HLA-DR、-DQ和-DP分型中的应用,重点关注其在器官移植领域的临床应用,特别是对于无关供体的骨髓移植。它现在能够明确鉴定所有HLA亚型,包括那些用其他方法无法识别的亚型,并且它是当前HLA分型方法的有力补充。最后,这种方法在HLA与疾病关联研究中被广泛使用,旨在表征参与自身免疫性疾病易感性或抗性的HLA II类表位。

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