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.

Frontiers in Microbiology
|January 28, 2021
PubMed

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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