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结核病中的宿主-病原体-外在因素:调节炎症与临床结局

The Host-Pathogen-Extrinsic Factors in Tuberculosis: Modulating Inflammation and Clinical Outcomes.

作者信息

Bastos Helder Novais, Osório Nuno S, Gagneux Sebastien, Comas Iñaki, Saraiva Margarida

机构信息

Department of Pneumology, Centro Hospitalar do São João, Porto, Portugal.

Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho, Braga, Portugal.

出版信息

Front Immunol. 2018 Jan 9;8:1948. doi: 10.3389/fimmu.2017.01948. eCollection 2017.

DOI:10.3389/fimmu.2017.01948
PMID:29375571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5767228/
Abstract

The already enormous burden caused by tuberculosis (TB) will be further aggravated by the association of this disease with modern epidemics, as human immunodeficiency virus and diabetes. Furthermore, the increasingly aging population and the wider use of suppressive immune therapies hold the potential to enhance the incidence of TB. New preventive and therapeutic strategies based on recent advances on our understanding of TB are thus needed. In particular, understanding the intricate network of events modulating inflammation in TB will help to build more effective vaccines and host-directed therapies to stop TB. This review integrates the impact of host, pathogen, and extrinsic factors on inflammation and the almost scientifically unexplored complexity emerging from the interactions between these three factors. We highlight the exciting data showing a contribution of this for the clinical outcome of TB and the need of incorporating it when developing novel strategies to rewire the immune response in TB.

摘要

结核病(TB)所造成的已然巨大的负担,将因该疾病与现代流行病(如人类免疫缺陷病毒和糖尿病)的关联而进一步加重。此外,人口老龄化加剧以及免疫抑制疗法的广泛应用有可能增加结核病的发病率。因此,需要基于我们对结核病最新认识进展的新预防和治疗策略。特别是,了解调节结核病炎症的复杂事件网络将有助于研发更有效的疫苗和宿主导向疗法来遏制结核病。本综述整合了宿主、病原体和外在因素对炎症的影响,以及这三个因素之间相互作用所产生的几乎尚未被科学探索的复杂性。我们强调了令人振奋的数据,这些数据显示了这一点对结核病临床结局的影响,以及在制定重新调整结核病免疫反应的新策略时纳入这一点的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b5/5767228/25e052e5f9d3/fimmu-08-01948-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b5/5767228/b944fef5890d/fimmu-08-01948-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b5/5767228/03d366418cba/fimmu-08-01948-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b5/5767228/25e052e5f9d3/fimmu-08-01948-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b5/5767228/b944fef5890d/fimmu-08-01948-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b5/5767228/03d366418cba/fimmu-08-01948-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b5/5767228/25e052e5f9d3/fimmu-08-01948-g003.jpg

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Pathogen lineage-based genome-wide association study identified CD53 as susceptible locus in tuberculosis.基于病原体谱系的全基因组关联研究发现 CD53 是结核病的易感基因座。
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Colonization with Helicobacter is concomitant with modified gut microbiota and drastic failure of the immune control of Mycobacterium tuberculosis.定植于幽门螺杆菌(Helicobacter)与肠道微生物群的改变以及结核分枝杆菌(Mycobacterium tuberculosis)免疫控制的严重失败同时发生。
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Epidemiology of Mycobacterium tuberculosis lineages and strain clustering within urban and peri-urban settings in Ethiopia.埃塞俄比亚城市和城郊环境中结核分枝杆菌谱系和菌株聚类的流行病学。
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Whole genomic sequencing based genotyping reveals a specific X3 sublineage restricted to Mexico and related with multidrug resistance.全基因组测序的基因分型揭示了一种特定的 X3 亚谱系,该亚谱系仅局限于墨西哥,与多种药物耐药性相关。
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