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变革性的结核病治疗:突破、挑战与未来的希望。

Revolutionizing tuberculosis treatment: Breakthroughs, challenges, and hope on the horizon.

作者信息

Kufa Martin, Finger Vladimir, Kovar Ondrej, Soukup Ondrej, Torruellas Carilyn, Roh Jaroslav, Korabecny Jan

机构信息

Faculty of Pharmacy in Hradec Kralové, Charles University, Hradec Kralove 50003, Czech Republic.

Biomedical Research Center, University Hospital Hradec Kralove, Hradec Kralove 50003, Czech Republic.

出版信息

Acta Pharm Sin B. 2025 Mar;15(3):1311-1332. doi: 10.1016/j.apsb.2025.01.023. Epub 2025 Jan 31.

DOI:10.1016/j.apsb.2025.01.023
PMID:40370552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12069392/
Abstract

Tuberculosis (TB), an infectious disease caused by the bacterium (), was responsible for the deaths of approximately 1.3 million people in 2022. In addition, 7.5 million new cases of TB have been reported. Present-day treatments require a daily dosing of a multiple-drug regimen for a minimum of six-month, but poor adherence and other factors often lead to treatment failure. Consequently, drug-resistant TB strains have become a growing concern, leading to more complex and expensive treatments. Promising drugs such as bedaquiline, delamanid, and pretomanid have been recently released, and 19 drug candidates are currently at different phases of clinical trials, addressing the problem of drug-resistant TB. Notwithstanding recent advances, the development of effective and safe drugs with novel mechanisms of action remains a challenge due to the unique nature of . Despite the persistent need for new treatments, TB research remains underfunded, highlighting the importance of collaborations between academia and the private sector in the advancement of anti-TB drug development. This review provides a perspective on the dynamic landscape of anti-TB drug discovery in recent years, offering hope for a more effective approach to combat this persistent global health threat.

摘要

结核病(TB)是由结核分枝杆菌引起的一种传染病,2022年约有130万人死于该病。此外,已报告750万例新的结核病病例。目前的治疗方法需要每天服用多种药物组成的治疗方案,至少持续六个月,但依从性差和其他因素常常导致治疗失败。因此,耐多药结核菌株已成为一个日益严重的问题,导致治疗更加复杂且费用更高。诸如贝达喹啉、地拉曼尼和普瑞马尼德等有前景的药物最近已获批上市,目前有19种候选药物正处于不同阶段的临床试验中,以解决耐多药结核病问题。尽管有这些最新进展,但由于结核分枝杆菌的独特性质,开发具有新作用机制的有效和安全药物仍然是一项挑战。尽管一直需要新的治疗方法,但结核病研究的资金仍然不足,这凸显了学术界和私营部门之间合作在推进抗结核药物开发方面的重要性。本综述对近年来抗结核药物发现的动态格局提供了一个视角,为更有效地应对这一持续存在的全球健康威胁带来了希望。

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b680/12069392/af2975aaf717/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b680/12069392/04f9c4356899/gr7.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b680/12069392/2a2e8e2b9df8/gr11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b680/12069392/04b405b04a3d/gr12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b680/12069392/e9559958a4f4/gr13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b680/12069392/41489a4c661c/gr14.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b680/12069392/1d19e95088a9/gr16.jpg

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本文引用的文献

1
What is the impact of the COVID-19 pandemic on tuberculosis?新冠疫情对结核病有何影响?
Lancet Glob Health. 2023 Sep;11(9):e1323-e1324. doi: 10.1016/S2214-109X(23)00360-1.
2
DprE2 is a molecular target of the anti-tubercular nitroimidazole compounds pretomanid and delamanid.DprE2 是抗结核硝基咪唑化合物丙硫异烟胺和德拉马尼的分子靶标。
Nat Commun. 2023 Jun 28;14(1):3828. doi: 10.1038/s41467-023-39300-z.
3
Design, synthesis and antitubercular activity of novel N-(amino)piperazinyl benzothiazinones with improved safety.新型 N-(氨基)哌嗪基苯并噻嗪酮的设计、合成及抗结核活性研究,安全性得到改善。
Eur J Med Chem. 2023 Oct 5;258:115545. doi: 10.1016/j.ejmech.2023.115545. Epub 2023 Jun 5.
4
Oxazolidinones as versatile scaffolds in medicinal chemistry.恶唑烷酮类化合物作为药物化学中用途广泛的骨架。
RSC Med Chem. 2023 Feb 8;14(5):823-847. doi: 10.1039/d2md00415a. eCollection 2023 May 25.
5
Tuberculosis: Pathogenesis, Current Treatment Regimens and New Drug Targets.结核病:发病机制、现行治疗方案及新药靶点。
Int J Mol Sci. 2023 Mar 8;24(6):5202. doi: 10.3390/ijms24065202.
6
Side-by-Side Profiling of Oxazolidinones to Estimate the Therapeutic Window against Mycobacterial Infections.唑烷酮类药物的并排分析,以估计针对分枝杆菌感染的治疗窗。
Antimicrob Agents Chemother. 2023 Apr 18;67(4):e0165522. doi: 10.1128/aac.01655-22. Epub 2023 Mar 15.
7
Cyclic AMP-Mediated Inhibition of Cholesterol Catabolism in by the Novel Drug Candidate GSK2556286.新型药物候选物 GSK2556286 通过环磷酸腺苷抑制 中的胆固醇分解代谢。
Antimicrob Agents Chemother. 2023 Jan 24;67(1):e0129422. doi: 10.1128/aac.01294-22. Epub 2023 Jan 5.
8
"Upcycling" known molecules and targets for drug-resistant TB.将已知的耐药结核病药物分子和靶点进行“升级利用”。
Front Cell Infect Microbiol. 2022 Oct 6;12:1029044. doi: 10.3389/fcimb.2022.1029044. eCollection 2022.
9
Whole Genome Sequencing Identifies Novel Mutations Associated With Bedaquiline Resistance in .全基因组测序鉴定与贝达喹啉耐药相关的新型突变体
Front Cell Infect Microbiol. 2022 May 27;12:807095. doi: 10.3389/fcimb.2022.807095. eCollection 2022.
10
Discovery and preclinical profile of sudapyridine (WX-081), a novel anti-tuberculosis agent.发现并初步研究沙达吡啶(WX-081)作为一种新型抗结核药物的特性。
Bioorg Med Chem Lett. 2022 Sep 1;71:128824. doi: 10.1016/j.bmcl.2022.128824. Epub 2022 May 27.