Personalized Phage Therapy in an ICU Patient with Polymicrobial Pulmonary Infections: a case from a single-arm trial

Yongxin Shi1, Jie Li2, Qian Yang3

  • 1Department of Critical Care Medicine, Shanghai Public Health Clinical Center, Fudan University, Shanghai, 201508, China.

Nature Communications
|July 27, 2026
PubMed

Insights

Phage therapy offers a promising approach for ventilator-associated infections (VAIs) caused by multidrug-resistant (MDR) pathogens. This case study shows personalized phage therapy provided transient control, reduced antibiotic use, and aided patient recovery.

Area of Science:

  • Infectious Diseases
  • Microbiology
  • Critical Care Medicine

Background:

  • Ventilator-associated infections (VAIs) caused by multidrug-resistant (MDR) pathogens present a significant challenge in intensive care units (ICUs).
  • Phage therapy is an emerging alternative for VAIs, but its effectiveness is influenced by various factors.

Purpose of the Study:

  • To report on the efficacy of tailored phage therapy as an adjunctive treatment for sequential MDR pulmonary infections in an ICU patient.
  • To evaluate the impact of phage therapy on clinical outcomes, inflammatory markers, and pathogen dynamics.

Main Methods:

  • A case report of a 40-year-old male ICU patient with sequential MDR Acinetobacter baumannii, Klebsiella pneumoniae, and Stenotrophomonas maltophilia pulmonary infections.
  • Seven rounds of personalized phage therapy, targeting single or dual pathogens, administered alongside antibiotics.
  • Monitoring of bacterial load, clinical symptoms, inflammatory markers (procalcitonin, IL-6, WBC, CRP), and pathogen susceptibility to phages.

Main Results:

  • Complete eradication of Acinetobacter baumannii was achieved.
  • Klebsiella pneumoniae and Stenotrophomonas maltophilia exhibited cyclical clearance and recurrence, attributed to strain replacement and phage resistance.
  • Phage therapy correlated with reduced bacterial load, fever, procalcitonin, and IL-6 levels, and improved pulmonary inflammation.
  • Limited response observed in white blood cell counts and C-reactive protein levels.
  • No severe adverse events were reported.

Conclusions:

  • Personalized phage therapy demonstrated transient control of MDR pathogens, extended intervention windows, and reduced reliance on high-level antibiotics.
  • Dynamic shifts in dominant pathogens influenced treatment outcomes, highlighting the complexity of VAI management.
  • The patient was successfully weaned from ventilation and discharged after six months, indicating the potential of phage therapy in mitigating MDR infections.