Suppr超能文献

药物重新利用用于治疗结核病:非甾体抗炎药的作用

Repurposing drugs for treatment of tuberculosis: a role for non-steroidal anti-inflammatory drugs.

作者信息

Maitra Arundhati, Bates Sadé, Shaik Monisha, Evangelopoulos Dimitrios, Abubakar Ibrahim, McHugh Timothy D, Lipman Marc, Bhakta Sanjib

机构信息

Mycobacteria Research Laboratory, Department of Biological Sciences,  Institute of Structural and Molecular Biology, Birkbeck, University of London, Malet Street, London WC1E 7HX, UK.

Centre for Clinical Microbiology, University College London, London NW3 2PF, UK.

出版信息

Br Med Bull. 2016 Jun;118(1):138-48. doi: 10.1093/bmb/ldw019. Epub 2016 May 5.

Abstract

INTRODUCTION

The number of cases of drug-resistant Mycobacterium tuberculosis, the causative agent of tuberculosis (TB), has risen rapidly in recent years. This has led to the resurgence in repurposing existing drugs, such as non-steroidal anti-inflammatory drugs (NSAIDs), for anti-TB treatment.

SOURCES OF DATA

Evidence from novel drug screening in vitro, in vivo, pharmacokinetic/pharmacodynamics analyses and clinical trials has been used for the preparation of this systematic review of the potential of NSAIDs for use as an adjunct in new TB chemotherapies.

AREAS OF AGREEMENT

Certain NSAIDs have demonstrated inhibitory properties towards actively replicating, dormant and drug-resistant clinical isolates of M. tuberculosis cells.

AREAS OF CONTROVERSY

NSAIDs are a diverse class of drugs, which have reported off-target activities, and their endogenous antimicrobial mechanism(s) of action is still unclear.

GROWING POINTS

It is essential that clinical trials of NSAIDs continue, in order to assess their suitability for addition to the current TB treatment regimen. Repurposing molecules such as NSAIDs is a vital, low-risk strategy to combat the trend of rapidly increasing antibiotic resistance.

摘要

引言

近年来,结核病的病原体——耐多药结核分枝杆菌病例数迅速上升。这导致人们重新关注现有药物,如非甾体抗炎药(NSAIDs),用于抗结核治疗。

数据来源

来自体外新药筛选、体内研究、药代动力学/药效学分析和临床试验的证据已被用于编写本系统评价,以评估NSAIDs作为新的结核病化疗辅助药物的潜力。

共识领域

某些NSAIDs已显示出对结核分枝杆菌细胞的活跃复制、休眠和耐药临床分离株具有抑制特性。

争议领域

NSAIDs是一类多样的药物,有报道称其存在脱靶活性,其内在抗菌作用机制仍不清楚。

发展要点

继续进行NSAIDs的临床试验至关重要,以便评估它们是否适合添加到当前的结核病治疗方案中。重新利用NSAIDs等分子是应对抗生素耐药性迅速增加趋势的重要且低风险策略。

相似文献

1
Repurposing drugs for treatment of tuberculosis: a role for non-steroidal anti-inflammatory drugs.
Br Med Bull. 2016 Jun;118(1):138-48. doi: 10.1093/bmb/ldw019. Epub 2016 May 5.
2
Non-steroidal anti-inflammatory drugs (NSAIDs) for chronic non-cancer pain in children and adolescents.
Cochrane Database Syst Rev. 2017 Aug 2;8(8):CD012537. doi: 10.1002/14651858.CD012537.pub2.
3
Non-steroidal anti-inflammatory drugs (NSAIDs) for cancer-related pain in children and adolescents.
Cochrane Database Syst Rev. 2017 Jul 24;7(7):CD012563. doi: 10.1002/14651858.CD012563.pub2.
4
5
Prophylactic non-steroidal anti-inflammatory drugs for the prevention of macular oedema after cataract surgery.
Cochrane Database Syst Rev. 2016 Nov 1;11(11):CD006683. doi: 10.1002/14651858.CD006683.pub3.
6
Non-steroidal anti-inflammatory drugs versus corticosteroids for controlling inflammation after uncomplicated cataract surgery.
Cochrane Database Syst Rev. 2017 Jul 3;7(7):CD010516. doi: 10.1002/14651858.CD010516.pub2.
7
WITHDRAWN: Non-aspirin, non-steroidal anti-inflammatory drugs for treating osteoarthritis of the knee.
Cochrane Database Syst Rev. 2007 Jul 18;2006(1):CD000142. doi: 10.1002/14651858.CD000142.pub2.
8
Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.
Cochrane Database Syst Rev. 2021 Apr 19;4(4):CD011535. doi: 10.1002/14651858.CD011535.pub4.
10
Xpert MTB/RIF assay for extrapulmonary tuberculosis and rifampicin resistance.
Cochrane Database Syst Rev. 2018 Aug 27;8(8):CD012768. doi: 10.1002/14651858.CD012768.pub2.

引用本文的文献

1
The advances in adjuvant therapy for tuberculosis with immunoregulatory compounds.
Front Microbiol. 2024 Jun 20;15:1380848. doi: 10.3389/fmicb.2024.1380848. eCollection 2024.
2
Repurposing an Antioxidant to Kill by Targeting the 50S Subunit of the Ribosome.
Biomolecules. 2023 Dec 14;13(12):1793. doi: 10.3390/biom13121793.
4
5
Vanoxerine kills mycobacteria through membrane depolarization and efflux inhibition.
Front Microbiol. 2023 Jan 26;14:1112491. doi: 10.3389/fmicb.2023.1112491. eCollection 2023.
6
Inhibition of indoleamine dioxygenase leads to better control of tuberculosis adjunctive to chemotherapy.
JCI Insight. 2023 Jan 24;8(2):e163101. doi: 10.1172/jci.insight.163101.
8
Structural Characterization of Multicomponent Crystals Formed from Diclofenac and Acridines.
Materials (Basel). 2022 Feb 17;15(4):1518. doi: 10.3390/ma15041518.

本文引用的文献

2
Inhaled drug treatment for tuberculosis: Past progress and future prospects.
J Control Release. 2016 Oct 28;240:127-134. doi: 10.1016/j.jconrel.2015.11.018. Epub 2015 Nov 18.
3
Tackling tuberculosis: Insights from an international TB Summit in London.
Virulence. 2015;6(6):661-72. doi: 10.1080/21505594.2015.1060396. Epub 2015 Jul 7.
4
Design and synthesis of novel anti-tuberculosis agents from the celecoxib pharmacophore.
Bioorg Med Chem. 2015 May 1;23(9):1935-43. doi: 10.1016/j.bmc.2015.03.041. Epub 2015 Mar 20.
5
Repurposing-a ray of hope in tackling extensively drug resistance in tuberculosis.
Int J Infect Dis. 2015 Mar;32:50-5. doi: 10.1016/j.ijid.2014.12.031.
6
Four-month moxifloxacin-based regimens for drug-sensitive tuberculosis.
N Engl J Med. 2014 Oct 23;371(17):1577-87. doi: 10.1056/NEJMoa1407426. Epub 2014 Sep 7.
7
TB Summit 2014: prevention, diagnosis, and treatment of tuberculosis-a meeting report of a Euroscicon conference.
Virulence. 2014 Jul 1;5(5):638-44. doi: 10.4161/viru.29803. Epub 2014 Jul 8.
9
DNA replication is the target for the antibacterial effects of nonsteroidal anti-inflammatory drugs.
Chem Biol. 2014 Apr 24;21(4):481-487. doi: 10.1016/j.chembiol.2014.02.009. Epub 2014 Mar 13.
10
Efflux inhibition with verapamil potentiates bedaquiline in Mycobacterium tuberculosis.
Antimicrob Agents Chemother. 2014;58(1):574-6. doi: 10.1128/AAC.01462-13. Epub 2013 Oct 14.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验