# Phage therapy in revision arthroplasty: State of the art and application protocols

**Authors:** Julius Michael Wolfgart, Hanno Schenker, Matthias Gatz, Filippo Migliorini, Joerg Eschweiler, Steffen Langwald, Hans-Peter Horz, Albrecht Eisert, Thomas Schwanz, Ulf Krister Hofmann

PMC · DOI: 10.1186/s42836-025-00355-6 · 2026-01-13

## TL;DR

This paper reviews the current state of phage therapy for treating joint infections after surgery, highlighting its potential and challenges.

## Contribution

The study provides updated guidelines for phage therapy application in periprosthetic joint infections.

## Key findings

- Phage therapy combined with antibiotics and surgery showed high success rates in elderly patients with knee or hip infections.
- Phage therapy was well tolerated, with only mild adverse effects reported.
- Clinical adoption is limited by regulatory barriers and lack of standardized protocols.

## Abstract

Periprosthetic joint infections (PJI) pose significant clinical challenges due to biofilm formation and antibiotic resistance. Standard treatment often involves implant removal and prolonged antibiotic therapy. Novel strategies target intracellular pathogens and biofilm-associated bacteria, including liposomal antibiotics, antimicrobial peptides, and bacteriophage therapy. Bacteriophages offer specificity and minimal disruption to human microbiota but remain experimental in PJI. Combining phages with targeted antibiotics shows promising results in preclinical models, though further research is needed to confirm efficacy in human PJI and optimise delivery methods.

This study updates the current evidence on the use of bacteriophages for patients with PJI, proposing guidelines for their clinical application.

PubMed was searched for articles containing phage therapy in revision arthroplasty. No additional filters or time constraints were used. All eligible studies were accessed by hand.

A total of 39 studies (20 clinical, 19 reviews) on phage therapy for PJI were analysed, covering 56 patients. Of those, negative outcomes were only reported in five. Most studies involved elderly patients with periprosthetic infections of the knee or hip and showed high success rates when combined with antibiotics and surgery. Phage therapy was well tolerated, with only mild adverse effects, such as fever and reversible transaminitis, occurring predominantly with intravenous administration. Review articles reveal that despite promising outcomes, challenges remain, including a lack of standardisation, limited clinical data, and regulatory hurdles.

This study highlights the potential of phage therapy for PJI, emphasising its high specificity, ability to target antibiotic-resistant bacteria, and capacity to disrupt biofilms, and provides a guideline for its clinical administration. Clinical adoption, however, remains limited by regulatory barriers, lack of standardised protocols, and insufficient trial data. Key steps for implementation include establishing regulatory frameworks, developing academic–industrial partnerships and reference centres, and identifying indications supported by controlled trials. With these in place, phage therapy could become a promising adjunct in managing periprosthetic joint infections.

Video Abstract

Video Abstract

The online version contains supplementary material available at 10.1186/s42836-025-00355-6.

## Linked entities

- **Diseases:** PJI (MONDO:0017380)

## Full-text entities

- **Genes:** IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TGFA (transforming growth factor alpha) [NCBI Gene 7039] {aka TFGA}
- **Diseases:** hepatic injury (MESH:D056486), contractures (MESH:D003286), hepatic impairment (MESH:D008107), and joints (MESH:D007592), Inflammatory (MESH:D007249), Pseudomonas aeruginosa (MESH:D011552), Fever (MESH:D005334), myocardial infarction (MESH:D009203), Pain (MESH:D010146), allergic reactions (MESH:D004342), knee infection (MESH:D000092443), bone erosion (MESH:D014077), musculoskeletal infections (MESH:D009140), chills (MESH:D023341), infections (MESH:D007239), Periprosthetic joint infection (MESH:D057068), Erythema (MESH:D004890), fistulas (MESH:D005402), aplastic anemia (MESH:D000741), osteomyelitis (MESH:D010019), MRSA (MESH:D013203), cytotoxicity (MESH:D064420), bleeding (MESH:D006470), infectious diseases (MESH:D003141), infections of soft tissue, bone (MESH:D018461), rheumatoid arthritis (MESH:D001172)
- **Chemicals:** DAC (MESH:D000077209), methicillin (MESH:D008712), cephalexin (MESH:D002506), rifampin (MESH:D012293), 99mTc (MESH:D013667), polymethylmethacrylate (MESH:D019904), Daptomycin (MESH:D017576), tigecycline (MESH:D000078304), Meropenem (MESH:D000077731), Doxycycline (MESH:D004318), Ciprofloxacin (MESH:D002939), Minocycline (MESH:D008911), Amoxicillin (MESH:D000658), Ceftriaxone (MESH:D002443), Ceftazidime (MESH:D002442), PFU (-), amoxicillin-clavulanate (MESH:D019980)
- **Species:** Bacteriophage sp. (species) [taxon 38018], Escherichia coli (E. coli, species) [taxon 562], Klebsiella pneumoniae (species) [taxon 573], Proteus mirabilis (species) [taxon 584], Pseudomonas aeruginosa (species) [taxon 287], Homo sapiens (human, species) [taxon 9606], Staphylococcus epidermidis (species) [taxon 1282], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Salmonella (genus) [taxon 590], Pseudomonas phage S (species) [taxon 1436831], Staphylococcus lugdunensis (species) [taxon 28035], Enterococcus faecalis (species) [taxon 1351], Staphylococcus aureus (species) [taxon 1280]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12797624/full.md

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Source: https://tomesphere.com/paper/PMC12797624