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Updated: Nov 19, 2025

Phage Therapy Application to Counteract Pseudomonas aeruginosa Infection in Cystic Fibrosis Zebrafish Embryos
Published on: May 12, 2020
Overcoming Challenges to Make Bacteriophage Therapy Standard Clinical Treatment Practice for Cystic Fibrosis
Renee N Ng1,2, Anna S Tai3,4, Barbara J Chang5
1School of Biomedical Sciences, The University of Western Australia, Perth, WA, Australia.
Abstract:
Individuals with cystic fibrosis (CF) are given antimicrobials as prophylaxis against bacterial lung infection, which contributes to the growing emergence of multidrug resistant (MDR) pathogens isolated. Pathogens such as Pseudomonas aeruginosa that are commonly isolated from individuals with CF are armed with an arsenal of protective and virulence mechanisms, complicating eradication and treatment strategies. While translation of phage therapy into standard care for CF has been explored, challenges such as the lack of an appropriate animal model demonstrating safety in vivo exist. In this review, we have discussed and provided some insights in the use of primary airway epithelial cells to represent the mucoenvironment of the CF lungs to demonstrate safety and efficacy of phage therapy. The combination of phage therapy and antimicrobials is gaining attention and has the potential to delay the onset of MDR infections. It is evident that efforts to translate phage therapy into standard clinical practice have gained traction in the past 5 years. Ultimately, collaboration, transparency in data publications and standardized policies are needed for clinical translation.
Insights
Phage therapy shows promise for cystic fibrosis (CF) lung infections, potentially delaying multidrug-resistant (MDR) pathogens. Primary airway cells offer a model to assess phage therapy safety and efficacy in CF patients.
Area of Science:
- Microbiology
- Pulmonology
- Bacteriophage Therapy
Background:
- Cystic fibrosis (CF) patients frequently receive antimicrobial prophylaxis, leading to multidrug-resistant (MDR) bacterial infections.
- Pseudomonas aeruginosa, a common CF pathogen, possesses significant protective and virulence mechanisms, hindering treatment.
- Current challenges in translating phage therapy into CF care include the lack of validated in vivo safety models.
Purpose of the Study:
- To review and provide insights into using primary airway epithelial cells as a model for assessing phage therapy safety and efficacy in the CF lung mucoenvironment.
- To highlight the potential of combining phage therapy with antimicrobials to combat MDR infections in CF.
- To discuss the progress and requirements for the clinical translation of phage therapy in CF.
Main Methods:
- Review of existing literature on phage therapy applications in cystic fibrosis.
- Discussion of the utility of primary airway epithelial cells to mimic the CF lung mucoenvironment.
- Exploration of the safety and efficacy of phage therapy, including combination approaches.
Main Results:
- Primary airway epithelial cells can serve as a relevant model to evaluate phage therapy's safety and efficacy in the context of CF lung conditions.
- Combining phage therapy with antimicrobials demonstrates potential in delaying the emergence of MDR infections.
- Significant traction has been observed in translating phage therapy into standard clinical practice over the last five years.
Conclusions:
- Phage therapy, particularly in combination with antimicrobials, presents a promising strategy to manage MDR bacterial infections in cystic fibrosis.
- The use of primary airway epithelial cells offers a viable alternative for preclinical safety and efficacy assessments.
- Clinical translation requires enhanced collaboration, transparent data sharing, and standardized policies.
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