# Bacteriophage Therapy: Current Strategies and Future Perspectives

**Authors:** Zihe Zhou, Hanyu Fu, Mengzhe Li, Zhongyu Han, Zhenchao Wu, Huahao Fan, Ning Shen, Jiajia Zheng

PMC · DOI: 10.1002/mco2.70645 · MedComm · 2026-03-01

## TL;DR

This paper reviews how bacteriophages can be used to treat drug-resistant infections, prevent hospital-acquired diseases, and develop vaccines, offering a modern alternative to antibiotics.

## Contribution

The paper systematically reviews the expanding scope of phage applications beyond traditional antibacterial use, including precision therapies and vaccine platforms.

## Key findings

- Phage therapy shows promise in treating multidrug-resistant infections and preventing hospital-acquired infections.
- Genetic engineering can broaden phage host ranges and convert temperate phages into lytic variants.
- Phages are effective in eliminating bacterial biofilms and controlling waterborne pathogens in hospital systems.

## Abstract

Antimicrobial resistance represents a significant global health threat, demanding alternative treatments beyond traditional antibiotics. Phage therapy has resurged as a promising solution to address this challenge. This manuscript offers an in‐depth examination of phage applications in clinical settings, encompassing the treatment of multidrug‐resistant infections, prevention of hospital‐acquired infections, and development of phage‐based vaccines. Advanced strategies are explored, including phage–antibiotic synergy, biomaterial‐enhanced delivery systems to improve phage stability, and the rational design of engineered phages to expand host range and optimize lytic efficacy. Additionally, the application of genetic engineering to broaden phage host ranges and convert temperate phages into lytic variants is discussed. In hospital infection prevention, phages demonstrate substantial potential, such as eliminating bacterial biofilms on medical devices, disinfecting environmental surfaces, and controlling waterborne pathogens in hospital water systems. Furthermore, phages offer a versatile platform for vaccine development, facilitating efficient antigen display and nucleic acid delivery. Despite progress, challenges persist in pharmacokinetics, standardized production, and regulatory approval. This review synthesizes recent preclinical and clinical developments, emphasizing the transformative potential of phage‐based therapies while acknowledging the barriers to their clinical implementation.

This manuscript systematically reviews the expanding scope of phage applications. It moves beyond traditional antibacterial use to explore their role in precision therapies against drug‐resistant infections, their synergy with antibiotics, and advanced biomaterial‐assisted delivery systems. The scope further extends to environmental decontamination (biofilm and water system control) and their innovative utility as versatile platforms for vaccine design, highlighting phages as multifaceted tools in medicine and biotechnology.

## Full-text entities

- **Genes:** Il4 (interleukin 4) [NCBI Gene 16189] {aka BSF-1, Il-4}, Vcp (valosin containing protein) [NCBI Gene 269523] {aka 3110001E05, CDC48, p97, p97/VCP}
- **Diseases:** Cystic fibrosis (MESH:D003550), cytotoxicity (MESH:D064420), UTI (MESH:D014552), E. coli infection (MESH:D004927), burn wound infections (MESH:D014946), chills (MESH:D023341), AMR (MESH:D060467), colitis (MESH:D003092), cancer (MESH:D009369), intra-abdominal infections (MESH:D059413), gastrointestinal infections (MESH:D005767), bacteremia (MESH:D016470), lung diseases (MESH:D008171), Klebsiella (MESH:D007710), immune abnormalities (MESH:D007154), dysbiosis (MESH:D064806), ischemic heart disease (MESH:D017202), biofilm infections (MESH:D007239), nonalcoholic fatty liver disease (MESH:D065626), pulmonary effusion (MESH:D000080324), P. aeruginosa (MESH:D011552), MDR (MESH:D018088), PD (MESH:D010300), colon cancer (MESH:D015179), viral infections (MESH:D014777), death (MESH:D003643), immunodeficient (MESH:D007153), catheter (MESH:D055499), fracture (MESH:D050723), influenza (MESH:D007251), melanoma (MESH:D008545), liver abscess (MESH:D008100), inflammation (MESH:D007249), diabetic foot ulcers (MESH:D017719), Nosocomial Infection (MESH:D003428), Wounds (MESH:D014947), lung infection (MESH:D012141), chronic pulmonary infections (MESH:D000088562), Clostridioides difficile infections (MESH:D003015), CBP (MESH:D011472), Allergy and Infectious Diseases (MESH:D003141), bloodstream infection (MESH:D018805), burn (MESH:D002056), MRSA (MESH:D013203), chronic otitis media (MESH:D010033), pulmonary or osteoarticular infections (MESH:D014394), fever (MESH:D005334), genetic disorder (MESH:D030342), neurological dysfunction (MESH:D009461), P. aeruginosa pneumonia (MESH:D011014), tumorigenesis (MESH:D063646), diarrhea (MESH:D003967), chronic osteomyelitis (MESH:D010019), stroke (MESH:D020521), chronic obstructive pulmonary disease (MESH:D029424), genitourinary infections (MESH:D014564), plague (MESH:D010930), tachycardia (MESH:D013610), IBD (MESH:D015212), organ damage (MESH:D000092124)
- **Chemicals:** indocyanine green (MESH:D007208), rifampicin (MESH:D012293), sodium hypochlorite (MESH:D012973), carbon (MESH:D002244), linezolid (MESH:D000069349), quinolones (MESH:D015363), agar (MESH:D000362), ciprofloxacin (MESH:D002939), HA (MESH:D017886), fluoroquinolones (MESH:D024841), nitrogen (MESH:D009584), PEI (MESH:D011094), cephalosporins (MESH:D002511), polysaccharide (MESH:D011134), stainless steel (MESH:D013193), poly(allylamine) (MESH:C063994), tetracycline (MESH:D013752), oxygen (MESH:D010100), alginate (MESH:D000464), chitosan (MESH:D048271), polyarginine (MESH:C015462), Poloxamer 407 (MESH:D020442), aminoglycoside (MESH:D000617), ceftazidime-avibactam (MESH:C000595613), Eudragit L100-55 (MESH:C446821), Pa (MESH:D011478), sulfur (MESH:D013455), Cefotaxime (MESH:D002439), clarithromycin (MESH:D017291), Benzalkonium chloride (MESH:D001548), AgNPs (-), TOP (MESH:C015535), H2O2 (MESH:D006861), ROS (MESH:D017382), chloride (MESH:D002712), hydroxyl radicals (MESH:D017665), methicillin (MESH:D008712), polyphosphate (MESH:D011122), chlorhexidine (MESH:D002710), hydrogen (MESH:D006859), (p)ppGpp (MESH:D006158), alcohol (MESH:D000438), polylysine (MESH:D011107), Silver nanoparticles (MESH:D012834), NB (MESH:D009556), PLGA (MESH:D000077182), beta-lactams (MESH:D047090), meropenem (MESH:D000077731), tetracyclines (MESH:D013754), OH (MESH:C031356), lipid (MESH:D008055), ceftazidime (MESH:D002442), polylactic acid (MESH:C033616), Carbapenem (MESH:D015780), vancomycin (MESH:D014640), triclosan (MESH:D014260), LPS (MESH:D008070), DNPs (MESH:D019297), polyglycolic acid (MESH:D011100), Pd (MESH:D010165)
- **Species:** Homo sapiens (human, species) [taxon 9606], H3N2 subtype (serotype) [taxon 119210], Clostridioides difficile (species) [taxon 1496], Klebsiella pneumoniae (species) [taxon 573], Acinetobacter nosocomialis (species) [taxon 106654], Pseudomonas aeruginosa (species) [taxon 287], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Mus musculus (house mouse, species) [taxon 10090], Staphylococcus aureus (species) [taxon 1280], Rattus norvegicus (brown rat, species) [taxon 10116], Stenotrophomonas maltophilia (species) [taxon 40324], Staphylococcus sp. MS2 (species) [taxon 1079236], Escherichia coli (E. coli, species) [taxon 562], Trichotorquatus sp. 5 (species) [taxon 2815555], Yersinia pestis (species) [taxon 632], H1N1 subtype (serotype) [taxon 114727], Simulium merga (species) [taxon 333337], Streptococcus pneumoniae (species) [taxon 1313], Staphylococcus haemolyticus (species) [taxon 1283], Hepatitis B virus (no rank) [taxon 10407], Influenza A virus (no rank) [taxon 11320], Bacteriophage sp. (species) [taxon 38018], Escherichia coli O121 (serogroup) [taxon 1055537], Enterococcus faecium (species) [taxon 1352], Acinetobacter baumannii (species) [taxon 470], Campylobacter jejuni (species) [taxon 197], Vibrio parahaemolyticus (species) [taxon 670], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Pseudomonas protegens (species) [taxon 380021], Bacillus anthracis (anthrax bacterium, species) [taxon 1392], Fusobacterium nucleatum (species) [taxon 851], Streptococcus gallolyticus (species) [taxon 315405], Enterococcus faecalis (species) [taxon 1351], Salmonella enterica (species) [taxon 28901], Erwinia amylovora (species) [taxon 552], Human papillomavirus 16 (serotype) [taxon 333760], Shigella (genus) [taxon 620], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986]
- **Cell lines:** MODE-K — Mus musculus (Mouse), Transformed cell line (CVCL_B4FG), phiMN1 — Mus musculus (Mouse), Hybridoma (CVCL_C7RB)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12950519/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12950519/full.md

## References

311 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950519/full.md

---
Source: https://tomesphere.com/paper/PMC12950519