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Phage Therapy in Combating Multidrug-Resistant Gram-Negative Pathogens: A Scoping Review.
Asif Sukri1, Bruno Silvester Lopes2,3, Alfizah Hanafiah4
1Department of Biological Sciences and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi 43600, Selangor, Malaysia.
Lytic bacteriophages show promise against multidrug-resistant Gram-negative bacteria like Klebsiella pneumoniae and Pseudomonas aeruginosa. However, more research is needed for Helicobacter pylori and larger human trials are crucial for clinical use.
Area of Science:
- * Microbiology
- * Infectious Diseases
- * Pharmacology
Background:
- * Rising threat of multidrug-resistant (MDR) Gram-negative pathogens: Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, and Helicobacter pylori.
- * Urgent need for novel therapeutic alternatives to combat these resistant infections.
Purpose of the Study:
- * To review current evidence on the efficacy of lytic bacteriophages against critical MDR Gram-negative pathogens.
- * To identify research gaps and challenges in the implementation of phage therapy.
Main Methods:
- * Scoping review of literature from 2015-2025, searching PubMed, Web of Science, and Scopus AI.
- * Inclusion of experimental and human studies on phage therapy for MDR, extensively drug-resistant (XDR), or pan-drug-resistant (PDR) strains.
- * Analysis of 172 selected articles.
Main Results:
- * Increasing research trend from 2015-2025, predominantly on K. pneumoniae, P. aeruginosa, and A. baumannii.
- * No eligible studies found for MDR H. pylori.
- * All studies confirmed lytic activity; phage cocktails were superior to single phages in some cases.
- * Demonstrated antibiofilm activity and successful bacterial reduction in animal models.
- * 87.5% of human case studies reported patient improvement or infection clearance.
Conclusions:
- * Lytic bacteriophages present a strong potential as a novel therapeutic strategy.
- * Significant challenges remain: lack of data for MDR H. pylori, heterogeneity in animal models, and limited large-scale human trials.
- * Future research should focus on standardization, mechanistic studies, and robust clinical trials for regulatory acceptance.
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