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人类对活动性和潜伏性结核病易感性的遗传学:现有知识和未来展望。

Genetics of human susceptibility to active and latent tuberculosis: present knowledge and future perspectives.

机构信息

Laboratory of Human Genetics of Infectious Diseases, INSERM U1163, Paris, France; Paris Descartes University, Imagine Institute, Paris, France; St Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York City, NY, USA.

School of Life Sciences, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland; SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland.

出版信息

Lancet Infect Dis. 2018 Mar;18(3):e64-e75. doi: 10.1016/S1473-3099(17)30623-0. Epub 2017 Oct 27.

Abstract

Tuberculosis is an ancient human disease, estimated to have originated and evolved over thousands of years alongside modern human populations. Despite considerable advances in disease control, tuberculosis remains one of the world's deadliest communicable diseases with 10 million incident cases and 1·8 million deaths in 2015 alone based on the annual WHO report, due to inadequate health service resources in less-developed regions of the world, and exacerbated by the HIV/AIDS pandemic and emergence of multidrug-resistant strains of Mycobacterium tuberculosis. Recent findings from studies of tuberculosis infection and of patients with Mendelian predisposition to severe tuberculosis have started to reveal human loci influencing tuberculosis outcomes. In this Review, we assess the current understanding of the contribution of host genetics to disease susceptibility and to drug treatment. Despite remarkable progress in technology, only a few associated genetic variants have so far been identified, strongly indicating the need for larger global studies that investigate both common and under-represented rare variants to develop new approaches to combat the disease. Pharmacogenomic discoveries are also likely to lead to more efficient drug design and development, and ultimately safer and more effective therapies for tuberculosis.

摘要

结核病是一种古老的人类疾病,据估计,它在几千年的时间里与现代人类一起起源和进化。尽管在疾病控制方面取得了相当大的进展,但结核病仍然是世界上最致命的传染病之一,根据世界卫生组织(WHO)的年度报告,仅在 2015 年,就有 1000 万例新发病例和 180 万人死亡,这主要是由于世界上欠发达地区的卫生服务资源不足,以及艾滋病毒/艾滋病大流行和耐多药结核分枝杆菌菌株的出现而加剧。最近对结核病感染和孟德尔易患严重结核病患者的研究结果开始揭示影响结核病结局的人类基因座。在这篇综述中,我们评估了宿主遗传学对疾病易感性和药物治疗的贡献的现有认识。尽管技术取得了显著进步,但迄今为止只确定了少数相关的遗传变异,这强烈表明需要进行更大规模的全球研究,以调查常见和代表性不足的罕见变异,从而开发新的方法来对抗这种疾病。药物基因组学的发现也可能导致更有效的药物设计和开发,并最终为结核病提供更安全、更有效的治疗方法。

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