Further Considerations on How to Improve Phage Therapy Experimentation, Practice, and Reporting: Pharmacodynamics Perspectives

被引:14
作者
Abedon, Stephen T. [1 ]
机构
[1] Ohio State Univ, Dept Microbiol, 1680 Univ Dr, Mansfield, OH 44906 USA
来源
PHAGE-THERAPY APPLICATIONS AND RESEARCH | 2022年 / 3卷 / 02期
关键词
bacteriophage therapy; half-life; inundative phage density; MOI; multiplicity of infection; pharmacology; LATENT-PERIOD EVOLUTION; LYSIS-INHIBITION; BACTERIOPHAGE; RESISTANCE; BIOCONTROL; COEXISTENCE; PERSISTENCE; ADSORPTION; BIOFILMS; KINETICS;
D O I
10.1089/phage.2022.0019
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Phage therapy uses bacterial viruses (bacteriophages) to infect and kill targeted pathogens. Approximately one decade ago, I started publishing on how possibly to improve upon phage therapy experimentation, practice, and reporting. Here, I gather and expand upon some of those suggestions. The issues emphasized are (1) that using ratios of antibacterial agents to bacteria is not how dosing is accomplished in the real world, (2) that it can be helpful to not ignore Poisson distributions as a means of either anticipating or characterizing phage therapy success, and (3) how to calculate a concept of 'inundative phage densities.' Together, these are issues of phage therapy pharmacodynamics, meaning they are ways of thinking about the potential for phage therapy treatments to be efficacious mostly independent of the details of delivery of phages to targeted bacteria. Much emphasis is placed on working with Poisson distributions to better align phage therapy with other antimicrobial treatments.
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页码:98 / 111
页数:14
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