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人类白细胞抗原(HLA)变异与疾病。

HLA variation and disease.

机构信息

Nuffield Department of Medicine, The Wellcome Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.

Australian Research Council Centre of Excellence for Advanced Molecular Imaging, Monash University, Wellington Road, Clayton, Victoria 3800, Australia.

出版信息

Nat Rev Immunol. 2018 May;18(5):325-339. doi: 10.1038/nri.2017.143. Epub 2018 Jan 2.

Abstract

Fifty years since the first description of an association between HLA and human disease, HLA molecules have proven to be central to physiology, protective immunity and deleterious, disease-causing autoimmune reactivity. Technological advances have enabled pivotal progress in the determination of the molecular mechanisms that underpin the association between HLA genetics and functional outcome. Here, we review our current understanding of HLA molecules as the fundamental platform for immune surveillance and responsiveness in health and disease. We evaluate the scope for personalized antigen-specific disease prevention, whereby harnessing HLA-ligand interactions for clinical benefit is becoming a realistic prospect.

摘要

自首次描述 HLA 与人类疾病之间的关联以来已经过去了五十年,HLA 分子已被证明是生理、保护性免疫和有害的、导致自身免疫反应疾病的核心。技术进步使确定 HLA 遗传学与功能结果之间关联的分子机制取得了关键进展。在这里,我们回顾了我们目前对 HLA 分子的理解,即作为健康和疾病中免疫监视和反应的基本平台。我们评估了针对个体抗原的疾病预防的范围,利用 HLA 配体相互作用获得临床益处正成为现实前景。

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