Use of Antimicrobial Photodynamic Therapy to Inactivate Multidrug-Resistant Klebsiella pneumoniae: Scoping Review

Angélica R Bravo1, Felipe Alejandro Fuentealba1, Iván A González2

  • 1Laboratorio de Microbiología Celular, Centro de Ciencias Médicas aplicadas, Facultad de Medicina y Ciencias de la Salud, Universidad Central de Chile, Lord Cochrane 418, Santiago 8330546, Chile.

Pharmaceutics
|January 8, 2025
PubMed

Insights

Antimicrobial photodynamic therapy (aPDT) effectively eliminates drug-resistant Klebsiella pneumoniae in lab studies. Further in vivo research is needed to confirm its potential as a complementary treatment for human infections.

Area of Science:

  • Microbiology
  • Photomedicine
  • Infectious Diseases

Background:

  • Klebsiella pneumoniae is a major cause of severe healthcare-associated infections.
  • Multi-drug resistant (MDR) strains, including ESBL and KPC producers, pose significant treatment challenges.
  • Conventional antibiotics are often ineffective against MDR K. pneumoniae.

Purpose of the Study:

  • To review the current applications of antimicrobial photodynamic therapy (aPDT) against Klebsiella pneumoniae.
  • To assess the efficacy of aPDT against both sensitive and MDR K. pneumoniae strains.
  • To identify research gaps in the use of aPDT for K. pneumoniae infections.

Main Methods:

  • A systematic scoping review following PRISMA-ScR guidelines.
  • Searches conducted in PubMed (MESH), Google Scholar, and Scopus databases (Jan 2012 - Sep 2024).
  • Inclusion of peer-reviewed articles in English detailing in vitro and in vivo aPDT studies on K. pneumoniae, including synergistic approaches.

Main Results:

  • 25 studies were included after screening 298 records.
  • aPDT demonstrated significant in vitro efficacy against sensitive and MDR K. pneumoniae.
  • Effectiveness was observed against biofilm-producing, ESBL, and KPC strains.

Conclusions:

  • aPDT shows promise as an effective antimicrobial therapy against Klebsiella pneumoniae.
  • Further in vivo studies are required to support potential human clinical applications.
  • aPDT can serve as a valuable adjunct to conventional antibiotic treatments.