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推动结核病控制生物标志物的应用。

Enabling biomarkers for tuberculosis control.

机构信息

Department of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany.

出版信息

Int J Tuberc Lung Dis. 2012 Sep;16(9):1140-8. doi: 10.5588/ijtld.12.0246.

Abstract

Accelerated control of tuberculosis (TB) requires better control measures. Biomarkers, which reliably diagnose active TB or even predict risk of disease progression in individuals, could facilitate rapid diagnosis and treatment of TB patients and allow preventive measures for latently infected individuals with a high risk of TB. Moreover, biomarkers could speed up clinical trials with novel drug and vaccine candidates. Three platforms of global biomarker profiling will be described, with an emphasis on the most recent achievements: transcriptomics, proteomics and metabolomics. Moreover, we will discuss the need for computational analyses to make the best use of the plethora of data generated by biomarker research. Aside from their potential prognostic and diagnostic value, biomarkers could provide deeper insight into pathological processes underlying disease, and hence form the basis for novel intervention measures that target host molecules and pathways. We propose that biosignatures, which discriminate active TB from both latent infection and uninfected status, as well as from other diseases, will become available within the next decade. However, simple, low-cost biomarker-based point-of-care diagnosis will probably not be achieved in the next few years.

摘要

加速结核病(TB)控制需要更好的控制措施。生物标志物可以可靠地诊断活动性结核病,甚至预测个体疾病进展的风险,从而有助于快速诊断和治疗结核病患者,并为具有高结核病风险的潜伏感染个体提供预防措施。此外,生物标志物可以加速新型药物和疫苗候选物的临床试验。本文将描述三个全球生物标志物分析平台,并重点介绍最新进展:转录组学、蛋白质组学和代谢组学。此外,我们还将讨论需要进行计算分析,以充分利用生物标志物研究产生的大量数据。除了具有潜在的预后和诊断价值外,生物标志物还可以深入了解疾病背后的病理过程,从而为针对宿主分子和途径的新型干预措施提供基础。我们提出,在未来十年内,能够区分活动性 TB 与潜伏感染和未感染状态以及其他疾病的生物标志物有望问世。然而,在未来几年内,可能无法实现基于简单、低成本生物标志物的即时护理诊断。

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