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针对耐多药结核病的宿主导向疗法。

Host-directed therapies for multidrug resistant tuberculosis.

作者信息

Zumla Alimuddin, Maeurer Markus

机构信息

Division of Infection and Immunity, University College London, NIHR Biomedical Research Center, UCL Hospitals NHS, Foundation Trust, London, UK.

Centre for Allogeneic Stem Cell Transplantation, Karolinska University Hospital Huddinge, Stockholm, Sweden.

出版信息

Int J Mycobacteriol. 2016 Dec;5 Suppl 1:S21-S22. doi: 10.1016/j.ijmyco.2016.09.044. Epub 2016 Nov 14.

DOI:10.1016/j.ijmyco.2016.09.044
PMID:28043559
Abstract

Tuberculosis (TB) causes 1.3 million deaths annually. There are 0.5 million cases of multidrug resistant TB (MDR-TB) and the number of cases is rising globally. The current status quo of the lengthy treatment duration and poor treatment outcomes associated with MDR/extensively drug-resistant TB, and those with comorbidity of TB with human immunodeficiency virus and noncommunicable diseases in sub-Saharan Africa is unacceptable. The TB drug pipeline remains sparse. New innovations for shortening the duration of therapy and improving treatment outcomes (cure and long-term functional disability due to lung damage) are urgently required. A wide range of host-directed therapies (HDT) are now available which require evaluation as adjuncts to current TB drug treatment. Examples are: The Host-directed Therapies Network consortium of 64 partners was launched in Cape Town after a meeting hosted by the South African Medical Research Council in April 2015. This network (which is open to anyone interested) plans to take forward a wide range of HDTs in randomized, placebo-controlled clinical trials as adjuncts to current TB treatment regimens with the aims of.

摘要

结核病每年导致130万人死亡。耐多药结核病病例有50万,且全球病例数正在上升。耐多药/广泛耐药结核病以及撒哈拉以南非洲地区结核病合并人类免疫缺陷病毒和非传染性疾病患者目前治疗疗程漫长且治疗效果不佳的现状令人无法接受。结核病药物研发进展仍然缓慢。迫切需要新的创新方法来缩短治疗疗程并改善治疗效果(治愈以及因肺部损伤导致的长期功能残疾)。现在有多种宿主导向疗法(HDT)可供评估,作为当前结核病药物治疗的辅助手段。例如:2015年4月在南非医学研究理事会主办的一次会议后,由64个合作伙伴组成的宿主导向疗法网络联盟在开普敦成立。该网络(对任何感兴趣的人开放)计划在随机、安慰剂对照临床试验中推进多种宿主导向疗法,作为当前结核病治疗方案的辅助手段,目标是……

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