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[评估结核病不同阶段——从发病到复发的生物标志物]

[Biomarkers to assess different aspects of tuberculosis--from development to relapse].

作者信息

Keicho Naoto

机构信息

National Center for Global Health and Medicine, 1-21-1, Toyama, Shinjuku-ku, Tokyo 162-8655, Japan.

出版信息

Kekkaku. 2010 Nov;85(11):823-8.

Abstract

Prevalence of tuberculosis (TB) has been decreased in Japan, whereas rapid increases in multi-drug resistance TB and HIV co-infection have raised serious problems in developing countries. To solve these problems, development of strong anti-TB vaccine, simple low-cost tools for diagnosis with drug sensitivity testing and new powerful anti-TB drugs is in urgent need. To evaluate new weapons against TB properly, appropriate biomarkers to assess the presence and severity of disease, response to treatment and prediction of relapse should be established. In case of TB, no relapse within two years after treatment is a gold standard to evaluate treatment outcome, but if we have a surrogate biomarker to predict relapse more quickly and accurately, clinical trials for TB drugs will be facilitated. A candidate TB vaccine may also be evaluated in a similar way. It may be further useful for individualized medicine to determine optimal dose and duration of TB treatment for each patient. I will review the current situation of biomarker studies and a new trend for development of biomarkers based on platforms of "omics" technology.

摘要

日本的结核病患病率已有所下降,而在发展中国家,耐多药结核病和艾滋病毒合并感染的迅速增加引发了严重问题。为解决这些问题,迫切需要研发强大的抗结核疫苗、用于药物敏感性检测的简单低成本诊断工具以及新型强效抗结核药物。为了正确评估对抗结核病的新武器,应建立适当的生物标志物,以评估疾病的存在和严重程度、对治疗的反应以及复发的预测。就结核病而言,治疗后两年内无复发是评估治疗效果的金标准,但如果我们有一个替代生物标志物能更快、更准确地预测复发,将有助于开展结核病药物的临床试验。候选结核疫苗也可以用类似的方法进行评估。确定每位患者结核病治疗的最佳剂量和疗程,对于个体化医疗可能会更有用。我将回顾生物标志物研究的现状以及基于“组学”技术平台的生物标志物开发新趋势。

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