Critical analysis of antibacterial agents in clinical development

生物 抗生素 铜绿假单胞菌 抗生素耐药性 不动杆菌 革兰氏阴性菌 抗药性 微生物学 细菌 重症监护医学 医学 大肠杆菌 遗传学 生物化学 基因
作者
Ursula Theuretzbacher,Karen Bush,Stéphan Harbarth,Mical Paul,John Rex,Evelina Tacconelli,Guy Thwaites
出处
期刊:Nature Reviews Microbiology [Springer Nature]
卷期号:18 (5): 286-298 被引量:249
标识
DOI:10.1038/s41579-020-0340-0
摘要

The antibacterial agents currently in clinical development are predominantly derivatives of well-established antibiotic classes and were selected to address the class-specific resistance mechanisms and determinants that were known at the time of their discovery. Many of these agents aim to target the antibiotic-resistant priority pathogens listed by the WHO, including Gram-negative bacteria in the critical priority category, such as carbapenem-resistant Acinetobacter, Pseudomonas and Enterobacterales. Although some current compounds in the pipeline have exhibited increased susceptibility rates in surveillance studies that depend on geography, pre-existing cross-resistance both within and across antibacterial classes limits the activity of many of the new agents against the most extensively drug-resistant (XDR) and pan-drug-resistant (PDR) Gram-negative pathogens. In particular, cross-resistance to unrelated classes may occur by co-selection of resistant strains, thus leading to the rapid emergence and subsequent spread of resistance. There is a continued need for innovation and new-class antibacterial agents in order to provide effective therapeutic options against infections specifically caused by XDR and PDR Gram-negative bacteria. New antibacterial agents are urgently needed to address the global increase in resistance. In this Review, Theuretzbacher and colleagues critically review the current published literature and publicly available information on antibacterial agents in all phases of clinical development.
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