Sintchenko Vitali, Timms Verlaine, Sim Eby, Rockett Rebecca, Bachmann Nathan, O'Sullivan Matthew, Marais Ben
Marie Bashir Institute for Infectious Diseases and Biosecurity, The University of Sydney, Sydney, NSW, Australia.
Centre for Infectious Diseases and Microbiology-Public Health, Westmead Hospital, Westmead, NSW, Australia.
Front Med (Lausanne). 2021 Apr 13;8:641260. doi: 10.3389/fmed.2021.641260. eCollection 2021.
Virulence arresting drugs (VAD) are an expanding class of antimicrobial treatment that act to "disarm" rather than kill bacteria. Despite an increasing number of VAD being registered for clinical use, uptake is hampered by the lack of methods that can identify patients who are most likely to benefit from these new agents. The application of pathogen genomics can facilitate the rational utilization of advanced therapeutics for infectious diseases. The development of genomic assessment of VAD targets is essential to support the early stages of VAD diffusion into infectious disease management. Genomic identification and characterization of VAD targets in clinical isolates can augment antimicrobial stewardship and pharmacovigilance. Personalized genomics guided use of VAD will provide crucial policy guidance to regulating agencies, assist hospitals to optimize the use of these expensive medicines and create market opportunities for biotech companies and diagnostic laboratories.
毒力抑制药物(VAD)是一类不断扩大的抗菌治疗药物,其作用是“解除”细菌的武装而非杀死细菌。尽管越来越多的VAD已注册用于临床,但由于缺乏能够识别最有可能从这些新药中获益的患者的方法,其应用受到了阻碍。病原体基因组学的应用有助于合理利用先进的传染病治疗方法。VAD靶点的基因组评估的发展对于支持VAD扩散到传染病管理的早期阶段至关重要。临床分离株中VAD靶点的基因组鉴定和表征可以加强抗菌药物管理和药物警戒。基于个性化基因组学指导使用VAD将为监管机构提供关键的政策指导,帮助医院优化这些昂贵药物的使用,并为生物技术公司和诊断实验室创造市场机会。