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Respir Med. 2023 Jan;206:107069. doi: 10.1016/j.rmed.2022.107069. Epub 2022 Dec 2.
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Tuberculosis (Edinb). 2023 Jan;138:102288. doi: 10.1016/j.tube.2022.102288. Epub 2022 Nov 29.
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Impact on Macrolide Resistance of Genetic Diversity of Mycobacterium abscessus Species.分支杆菌属脓肿亚种遗传多样性对大环内酯类耐药性的影响。
Microbiol Spectr. 2022 Dec 21;10(6):e0274922. doi: 10.1128/spectrum.02749-22. Epub 2022 Nov 23.
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用于治疗复杂感染的一氧化氮供体型前药。

Nitric oxide-releasing prodrug for the treatment of complex infections.

机构信息

Vast Therapeutics, Durham, North Carolina, USA.

Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

出版信息

Antimicrob Agents Chemother. 2024 Feb 7;68(2):e0132723. doi: 10.1128/aac.01327-23. Epub 2024 Jan 11.

DOI:10.1128/aac.01327-23
PMID:38206003
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10848776/
Abstract

Non-tuberculosis mycobacteria (NTM) can cause severe respiratory infection in patients with underlying pulmonary conditions, and these infections are extremely difficult to treat. In this report, we evaluate a nitric oxide (NO)-releasing prodrug [methyl tris diazeniumdiolate (MD3)] against a panel of NTM clinical isolates and as a treatment for acute and chronic NTM infections . Its efficacy in inhibiting growth or killing mycobacteria was explored alongside evaluation of the impact to primary human airway epithelial tissue. Airway epithelial tissues remained viable after exposure at concentrations of MD3 needed to kill mycobacteria, with no inherent toxic effect from drug scaffold after NO liberation. Resistance studies conducted via serial passage with representative isolates demonstrated no resistance to MD3. When administered directly into the lung via intra-tracheal administration in mice, MD3 demonstrated significant reduction in bacterial load in both acute and chronic models of lung infection. In summary, MD3 is a promising treatment for complex NTM pulmonary infection, specifically those caused by , and warrants further exploration as a therapeutic.

摘要

非结核分枝杆菌(NTM)可导致肺部基础疾病患者发生严重的呼吸道感染,且这些感染极难治疗。在本报告中,我们评估了一种一氧化氮(NO)释放前药[甲基三叠氮烯二醇(MD3)]针对一组 NTM 临床分离株的疗效,并将其作为急性和慢性 NTM 感染的治疗方法。我们探讨了其抑制分枝杆菌生长或杀灭分枝杆菌的效果,并评估了对原代人呼吸道上皮组织的影响。在需要杀死分枝杆菌的 MD3 浓度下暴露后,气道上皮组织仍保持存活,且 NO 释放后药物支架无固有毒性作用。通过对代表性分离株进行连续传代的耐药性研究表明,MD3 对其无耐药性。当通过气管内给药直接施用于肺部时,MD3 在急性和慢性肺部感染模型中均显著降低了细菌负荷。总之,MD3 是一种有前途的治疗复杂 NTM 肺部感染的方法,特别是由 引起的感染,值得进一步探索作为一种治疗方法。