HLA表位-我们准备好临床黄金时间了吗?历史观点和未来需求。

Clinical transplants Pub Date : 2016-01-01
Reut H Dvorai, David F Pinelli, Anat R Tambur
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引用次数: 0

摘要

长期移植成功的一个重要障碍是供体特异性人白细胞抗原(HLA)抗体的发展。将产生这种抗体的风险降至最低的最佳方法是HLA相同的移植,但找到这种器官的可能性非常低。另一种方法是鉴定“允许错配”——HLA抗原错配不太可能引起免疫反应。在过去几年中,很明显,在“表位水平”上进行匹配是可能的解决方案;然而,我们仍然在如何定义HLA表位的问题上挣扎。在此,我们提供了一个简短的回顾表位概念的发展在HLA领域,希望它能阐明目前的知识。接下来,我们就未来将引领我们走向何方发表个人看法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HLA Epitopes - Are We Ready for Clinical Prime Time? Historic Perspective and Future Needs.

A significant barrier to long-term transplant success is the development of de novo donor-specific human leukocyte antigen (HLA) antibodies. The best approach to minimize the risk of developing such antibodies is an HLA identical transplant, but the likelihood of finding such an organ is very low. The alternative is to identify "permissible mismatches" - HLA antigen mismatches that are less likely to induce an immune response. In the past few years, it has become clear that matching at the "epitope level" is the likely solution; however, we are still struggling with how to define HLA epitopes. Herein, we provide a short review of the development of the epitope concept within the HLA field, with the hope that it sheds light on present knowledge. We follow with our personal opinion on where the future is leading us.

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