The future of antibiotics begins with discovering new combinations

被引:34
|
作者
Zhu, Meilin [1 ,2 ]
Tse, Megan W. [1 ,2 ]
Weller, Juliane [2 ]
Chen, Julie [1 ,2 ,3 ]
Blainey, Paul C. [1 ,2 ,4 ]
机构
[1] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[2] Broad Inst MIT & Harvard, 415 Main St, Cambridge, MA 02142 USA
[3] MIT, Microbiol Grad Program, Cambridge, MA 02139 USA
[4] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
antibiotics; antibacterials; drug combinations; antibiotic resistance; microfluidics; MYCOBACTERIUM-TUBERCULOSIS; SYNTHETIC LETHALITY; DRUG-COMBINATIONS; SYNERGY; THERAPY; SPECIFICITY; SENSITIVITY; MECHANISMS; CHALLENGES; RESISTANCE;
D O I
10.1111/nyas.14649
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Antibiotic resistance is a worldwide and growing clinical problem. With limited drug development in the antibacterial space, combination therapy has emerged as a promising strategy to combat multidrug-resistant bacteria. Antibacterial combinations can improve antibiotic efficacy and suppress antibacterial resistance through independent, synergistic, or even antagonistic activities. Combination therapies are famously used to treat viral and mycobacterial infections and cancer. However, antibacterial combinations are only now emerging as a common treatment strategy for other bacterial infections owing to challenges in their discovery, development, regulatory approval, and commercial/clinical deployment. Here, we focus on discovery-where the sheer scale of combinatorial chemical spaces represents a significant challenge-and discuss how combination therapy can impact the treatment of bacterial infections. Despite these challenges, recent advancements, including new in silico methods, theoretical frameworks, and microfluidic platforms, are poised to identify the new and efficacious antibacterial combinations needed to revitalize the antibacterial drug pipeline.
引用
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页码:82 / 96
页数:15
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