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Updated: Oct 25, 2025

Author Spotlight: Investigating Bacteriophage-Induced Immune Responses in Gnotobiotic Mice
Published on: January 26, 2024
Bacterial lysis, autophagy and innate immune responses during adjunctive phage therapy in a child
Ameneh Khatami1,2, Ruby C Y Lin2,3,4, Aleksandra Petrovic-Fabijan3
1Department of Infectious Diseases and Microbiology, The Children's Hospital at Westmead, Westmead, NSW, Australia.
Insights
Adjunctive phage therapy successfully treated a child
Area of Science:
- Pediatric infectious diseases
- Bacteriophage therapy
- Osteoarticular infections
Background:
- Chronic Pseudomonas aeruginosa osteoarticular infections pose significant treatment challenges.
- Phage therapy offers a potential alternative or adjunctive treatment strategy.
Observation:
- Real-time monitoring of phage and bacterial kinetics guided treatment adjustments.
- Host immune response markers were tracked alongside therapeutic efficacy.
Findings:
- Adjunctive phage therapy showed a significant therapeutic effect within two weeks.
- Early treatment correlated with bacterial cell release, transient systemic inflammation, and immune gene upregulation.
- Both innate and adaptive immune responses were activated during therapy.
Implications:
- Phage therapy, guided by kinetic monitoring, can be effective for severe pediatric bone infections.
- Understanding host-pathogen dynamics is crucial for optimizing phage therapy.
- This case highlights the potential of phage therapy in managing antibiotic-resistant infections.
Abstract:
Adjunctive phage therapy was used in an attempt to avoid catastrophic outcomes from extensive chronic Pseudomonas aeruginosa osteoarticular infection in a 7-year-old child. Monitoring of phage and bacterial kinetics allowed real-time phage dose adjustment, and along with markers of the human host response, indicated a significant therapeutic effect within two weeks of starting adjunctive phage therapy. These findings strongly suggested the release of bacterial cells or cell fragments into the bloodstream from deep bony infection sites early in treatment. This was associated with transient fever and local pain and with evidence of marked upregulation of innate immunity genes in the host transcriptome. Adaptive immune responses appeared to develop after a week of therapy and some immunomodulatory elements were also observed to be upregulated.
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