The changing landscape of HLA typing: Understanding how and when HLA typing data can be used with confidence from bench to bedside

被引:9
作者
Baxter-Lowe, Lee Ann [1 ,2 ]
机构
[1] Childrens Hosp Los Angeles, Dept Pathol & Lab Med, Los Angeles, CA 90027 USA
[2] Univ Southern Calif, Dept Pathol, Los Angeles, CA 90007 USA
关键词
HUMAN-LEUKOCYTE ANTIGEN; C EXPRESSION; CLASS-I; HIGH-RESOLUTION; ALLELES; GENES; IDENTIFICATION; ASSOCIATIONS; POLYMORPHISM; TRANSCRIPTS;
D O I
10.1016/j.humimm.2021.04.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human leukocyte antigen (HLA) genes are extraordinary for their extreme diversity and widespread impact on human health and disease. More than 30,000 HLA alleles have been officially named and more alleles continue to be discovered at a rapid pace. HLA typing systems which have been developed to detect HLA diversity have advanced rapidly and are revolutionizing our understanding of HLA's clinical importance. However, continuous improvements in knowledge and technology have created challenges for clinicians and scientists. This review explains how differences in HLA typing systems can impact the HLA types that are assigned. The consequences of differences in laboratory testing methods and reference databases are described. The challenges of using HLA types that are not equivalent are illustrated. A fun-damental understanding of the continual expansion of our understanding of HLA diversity and limita-tions in some of the typing data is essential for using typing data appropriately in clinical and research settings. (C) 2021 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:466 / 477
页数:12
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