A Short History of B-Cell HLA Epitopes

Ilias Doxiadis, H. Loeffler-Wirth, Nils Lachmann, Claudia Lehmann
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Abstract

Background: HLA epitopes are currently in the focus of transplantation immunogenetics. The main reason is the complexity of the HLA system with >38,000 alleles, the number of which increases steadily. These alleles are determined by the current state-of-the art typing methods like second- and third-generation sequencing. Screening for HLA antibodies is hampered by the lack of specific target beads with all possible alleles described. Summary: A way to circumvent the problem is to define HLA epitopes. The number of antibody-confirmed epitopes, on the other hand, was found to be 72 for HLA class I and 74 for HLA class II. Here, we elaborate on the current knowledge on these HLA epitopes. Absolute definitions of these structures are not yet available. Key Messages: Making use of eplets is a comparable way allowing statistical analyses. However, one should keep in mind that the results obtained are approximative or perhaps better associative. Continuous collaboration is needed for the full understanding of the HLA epitopes. The reactivity toward epitopes remains patient-specific.
B 细胞 HLA 表位简史
背景:HLA 表位目前是移植免疫遗传学的焦点。主要原因是 HLA 系统非常复杂,有超过 38,000 个等位基因,而且数量还在不断增加。目前最先进的分型方法(如第二代和第三代测序)可以确定这些等位基因。由于缺乏描述所有可能等位基因的特异性靶珠,HLA 抗体的筛选受到了阻碍。摘要:规避这一问题的方法是定义 HLA 表位。另一方面,经抗体确认的表位数量,HLA I 类为 72 个,HLA II 类为 74 个。在此,我们将详细阐述目前有关这些 HLA 表位的知识。目前还没有这些结构的绝对定义。关键信息:使用表位是进行统计分析的一种可比方法。然而,我们应该记住,所获得的结果是近似的,或者说是联想的。要全面了解 HLA 表位,还需要继续合作。对表位的反应性仍然因患者而异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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