Abstract
Urinary tract infections (UTIs) are a problem worldwide, affecting almost half a billion people each year. Increasing antibiotic resistance and limited therapeutic options have led to the exploration of alternative therapies for UTIs, including bacteriophage (phage) therapy. This systematic review aims at evaluating the efficacy of phage therapy in treating UTIs. We employed a comprehensive search strategy for any language, any animal, and any publication date. A total of 55 in vivo and clinical studies were included. Of the studies, 22% were published in a non-English language, 32.7% were before the year 1996, and the rest were after 2005. The results of this review suggest that phage therapy for UTIs can be effective; more than 72% of the included articles reported microbiological and clinical improvements. On the other hand, only 5 randomized controlled trials have been completed, and case reports and case series information were frequently incomplete for analysis. Overall, this comprehensive systematic review identifies preliminary evidence supporting the potential of phage therapy as a safe and viable option for the treatment of UTIs.
Introduction
Urinary tract infections (UTIs) are a global health concern, contributing to 404.6 million cases annually in both males and females, with 236,786 deaths. 1 Approximately 50% of women will get a UTI at least once in their lifetime, and of those, 20–30% will have a recurrence. 2 Consequently, UTIs act as a driver for the development of antimicrobial resistance (AMR), affecting quality of life and creating a massive clinical and economic burden. 3
Threats from superbugs and AMR associated with UTIs have rekindled interest in viruses that exclusively target bacteria (bacteriophages, commonly known as phages). 4 A century after their discovery, bacteriophages are now receiving attention as a promising solution to AMR. First, bacteriophages interact specifically with their bacterial host and have a narrow spectrum of activity.
Accordingly, compared with antibiotics, phages cause less harm to patients' microbiota. 5 While the interaction specificity is challenging in cases of polymicrobial infections, as they would require administering more than one phage, this is not a hurdle in UTIs as they are not primarily polymicrobial in nature at time of diagnosis. 6 Second, phage therapy is characterized by auto-dosing, as phages are self-replicating at the site of infection as long as susceptible target bacteria are nearby. 7 Third, there is evidence that phages are more effective than antibiotics in the treatment of biofilms associated with UTIs,8–10 which are important contributors to antibiotic treatment failure and recurrence.3,11
Between the 1940s and 1970s, lack of widespread knowledge about phages in combination with the rise of the golden age of antibiotic discovery led to the abandonment of phage therapy in Western Europe and in the United States. However, Eastern Europe and the former Soviet republics continued experimenting with phages and using them for therapy. 12
In the past three decades, the prevalence of antibiotic-resistant superbugs and the lack of novel classes in the antibiotic pipeline has led to a revival of phage therapy globally, with multiple centres now building on the long-standing experience from Poland and the former Soviet Union. 13 These centers, in addition to regulatory bodies, are looking for animal studies (preclinical) to support phage clinical trials in humans. So, a targeted systematic review on phage therapy in urinary infections in humans and laboratory animals will assist further study and phage therapy protocol development.
Four phage therapy narrative reviews and a systematic review with a small section on UTI management have been published (Table 1), but these are limited in scope with respect to timeframe, language, and/or research subjects.14–18 Thus, we sought to generate a comprehensive systematic review that includes both a One Health lens and non-English language publications on the role of phages as a suitable alternative or adjuvant therapy for managing UTIs in humans and animals.
Literature Reviews Covering Bacteriophage Therapy for Urinary Tract Infections
UPEC, uropathogenic Escherichia coli; UTI, urinary tract infection.
A systematic review was conducted in conformity with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines (summarized in Supplementary Table S1) and following Cochrane methodology. 19 First, a preliminary search was conducted on November 20, 2022, in ERO, PubMed, and the Cochrane library to identify overlap among published and registered systematic reviews (summarized in Table 1).
Methods
Search methods
An information specialist and health science librarian (co-author J.M.) in consultation with the review team identified peer-reviewed literature using a comprehensive search strategy. The PRISMA-Search extension developed by Rethlefsen et al. 19a has been used to report all search strategies. To minimize search errors and enhance comprehensiveness, a health science librarian peer-reviewed the search strategy following the Peer Review of Electronic Search Strategies (PRESS) form. 20 Relevant subject headings and text words related to the following concepts were included in the search: “phage” therapy and “UTI.” For comprehensiveness, no date, language, or design limits were applied.
A protocol was registered in PROSPERO database (ID CRD4202231927); the search strategy was developed and finalized in OVID Medline, and then translated to OVID Embase, EBSCO CINAHL, the Cochrane Library, Scopus, and Global Index Medicus.
The search was run on March 18, 2022, and rerun on November 17, 2022. The articles were exported into Endnote, de-duplicated, and then imported into Covidence (Covidence systematic review software, Veritas Health Innovation, Melbourne, Australia. Available at www.covidence.org) for screening. The full search strategies can be viewed here: https://doi.org/10.5683/SP3/WIVREO
Gray literature was identified by manually searching relevant gray literature databases, catalogues, and search engines, including ClinicalTrials.gov, WHO International Clinical Trials Registry Platform, Open Grey, TripPro, and OSIster. The gray literature search documentation can be located here: https://doi.org/10.5683/SP3/WIVREO
The reference lists of included articles were also searched. In September and October 2022, P.B.H. conducted a supplementary search of each primary article's references and citing articles to obtain studies missing from the initial search. Reference searching was conducted initially using Spidercite (Available at https://sr-accelerator.com/#/spidercite), while not possible, Web of Science and Scopus were used for the remaining articles.21,22
On November 18, 2022, the search results were input directly into Covidence and automatically deduplicated. Next, the articles underwent title and abstract screening and a full-text review as described earlier. A total of six results from the supplementary search were advanced to the data extraction stage.
Study selection (inclusion and exclusion criteria)
Before the title-abstract and full-text screening processes (A.M.A., P.B.H., and G.J.G.) performed a pilot test with at least 10% of the articles to ensure reviewers were mostly in agreement regarding the eligibility criteria. The initial round of title and abstract screening was performed by two independent reviewers (A.M.A. and P.B.H.), with a third reviewer (G.J.G.) resolving disagreements. Full manuscripts were next obtained and uploaded to a shared cloud-based repository for access by all reviewers. Articles that were published in languages other than English were converted from PDF to Word using the Optical Character Recognition (OCR) program by Convertio (see https://convertio.co/) and translated using Google Translate (available at https://translate.google.ca/). 23
EurekaMag (see https://eurekamag.com/), a scholarly article and abstract supply service, was used to access five articles. Articles were assessed as eligible based on the study design, the condition being studied, population, intervention, comparator, and outcomes (Fig. 1). After all articles from the initial search were obtained, eligibility screening of the full-text manuscripts was conducted with two independent reviewers (P.B.H. and A.M.A. or G.J.G.). A third reviewer (A.P.H.) was the adjudicator on the eligibility and the reason for exclusion.
Systematic review characteristics at a glance.
Data extraction
One reviewer (P.B.H.) completed data extraction using Google Sheets, and each of the extractions was validated by another reviewer (A.M.A.). In cases of missing information, Supplementary Material was reviewed, and efforts were made to contact the authors. A third reviewer (A.P.H.) was consulted on areas of disagreement.
Data retrieved from the selected studies included: language, method of study, participant's demographics (age, gender, and type of animal or animal model), baseline characteristics (organism of infection, type of infection, and previous treatments), study design/regimen (selected phage(s), phage origin or isolation source, nucleic acid sequence GenBank number, route, concentration, timing, dosing, frequency, and additional therapeutics), and measures of effect (microbiological outcomes, clinical outcomes, and presence of phage resistance).
Critical appraisal
The Joanna Briggs Institute Critical Appraisal Checklist was used to evaluate case series and case reports. 24 For case reports and case series to be accepted, they needed to receive at least five categories with “Yes” or “Unclear.” Critical appraisal of the human randomized control trials (RCTs) was performed using the Critical Appraisal Skills Program (CASP) Checklist.25,26 Human RCTs needed to meet the threshold of at least eight categories with “Yes” or “Unclear” to be accepted. If a study did not meet these thresholds during the critical appraisal, then they were marginally accepted. Each study was evaluated independently by two reviewers (J.D.C. and P.B.H.). Discrepancies in the decision to include or exclude studies were reviewed and resolved by an additional reviewer (G.J.G.).
Results
Study characteristics
The initial data search returned 3138 search results, leaving 1805 manuscripts to be screened after de-duplication for title and abstract. Following this, 103 studies were assessed for eligibility; 55 articles fulfilled the selection criteria and were included in the systematic review (Fig. 2). Most studies were published in English (n = 43) or Russian (n = 8).
PRISMA flow chart summarizing the study selection process. PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses.
Two articles were published in French and two in Mandarin. Regarding the method of study, 34.5% (n = 19/55) were case series, 25.4% (n = 14/55) were case reports, 7.2% (n = 4/55) were RCTs, 12.7% (n = 7/55) were non-randomized control clinical trials (non-RCT clinical trial), and 20.0% (n = 11/55) were preclinical studies (Table 2). Included articles were published between 1926 and 2022 (Fig. 3), 37 articles were published after 2005, and the rest (18/55) were published before 1996.
Urinary tract infection phage therapy studies by decade (n = 55). RCT, randomized control trial; Preclinical, studies designed to evaluate the effectiveness of a treatment for an animal model; Veterinary RCT, RCT designed to evaluate the effectiveness of an intervention for an animal; Human non-RCT clinical trial, human trial that does not include an element of randomization; Case report, report of the symptoms, diagnosis, treatment, and follow-up of an individual patient; Case series, report of the symptoms, diagnosis, treatment, and follow-up of several patients.
Studies Assessing the Safety and Efficacy of Phage Therapy in Managing Urinary Tract Infections (27–81)
See Supplementary Table S2 for the comprehensive data extraction sheet.
A total of 12 patients received phage therapy, but little detail was provided.
Microbiological or clinical improvements were observed, but statistical significance was not achieved.
MOI, multiplicity of infection; NS, not specified in the study.
Human/animal subject characteristics
Of the studies, 14.6% were performed on mice (n = 2703), with the rest as follows: 1.82% in guinea pigs (n = 37), 1.82% in Nile tilapia (n = 120), and 81.8% were performed in humans (n = at least 2083), where “n” is the actual number of subjects involved. One article 27 published in 2021 mentioned that the number of included patients was “<30,” whereas three other studies published in 1932, 1960, and 198328–30 failed to specify the number of patients.
Most infections, accounting for 38.2% (21/55) of the included studies, were caused by Escherichia coli, as either a mono- or polymicrobial infection. Other pathogens included Acinetobacter baumannii, Citrobacter spp., Cronobacter turicensis, Enterococcus faecalis, Klebsiella pneumoniae, Salmonella enteritidis, Staphylococcus aureus, Shigella flexneri, Pseudomonas aeruginosa, Proteus mirabilis, and Proteus vulgaris.
There was a single study that failed to specify the infectious organism. Patients were treated previously with antibiotics (n = 18/55), surgeries (n = 5/55), but in 17 articles previous treatments were not specified.
Phage characteristics
Among the 55 articles included, 13 reported using a single phage, 4 studies used 2 phages, and 9 studies used 3 or more phages. The remaining 29 articles did not specify the number of phages used. In eight studies, phages were purified by ultracentrifugation, one study by filter sterilization, one by anion exchange concentration and then dialyzed followed by filter sterilization. Only seven articles specified accession numbers for the phage genome in GenBank or other repositories. Phages were used at concentrations from 104 plaque-forming units per mL (PFU/mL) up to 3 × 1011 PFU/mL.
Phages were introduced via different routes, with 36.3% (20/55) using an intravesicular approach such as bladder instillation, bladder injection, bladder irrigation, or bladder lavage. Phages were given via a single route or through a combination of different routes, including intraperitoneally, subcutaneously, kidney instillation, transurethrally, intrarectally, and orally.
Only in 3.6% of the articles (2/55) were phages given intravenously, and both were recent case reports.31,32 In one study, bladder instillation was compared with intrarectal or both routes of administration concurrently. 33 Phages were also given topically, via cystostomy, and intravesically with or without vaginal administration.
Nine studies failed to specify the route of administration. Phages were given at various frequencies; once, twice, or three times daily; once every 2 days, once every week, or two times weekly. Frequency of phage administration was not identified in 17 trials, and the duration of phage administration ranged from 1 day to 19 weeks.
In many trials, phages were given in addition to other therapeutics, including toxoids, autovaccines, anesthetics, surgical treatments, the herbal product Centella asiatica, phage encoded polymerases as depolymerase Dep-ORF8, and antibiotics.
The antibiotics administered included ceftazidime, meropenem, imipenem/amikacin, imipenem/cilastatin, amikacin, colistin (polymyxin E), polymyxin B, fosfomycin, third-generation cephalosporin; ceftriaxone, ertapenem, fluoroquinolones, ciprofloxacin, neomycin, colimycin, trimethoprim-sulfamethoxazole (SMZ-TMP), piperacillin-tazobactam, ceftriaxone, and amoxicillin/clavulanic acid. In 11 RCTs, 4 case reports, 3 case series, and 2 clinical trials, no additional therapeutics were given with phages.
Efficacy of phage therapy
In most articles, phage administration resulted in microbiological and clinical improvements (78.2% (43/55) and 72.7% (40/55), respectively). In terms of microbiological effectiveness, 62% of the articles (34/55) reported complete bacterial eradication, urine sterilization, bacterial levels below the limit of detection, or a negative result for culture growth.
The treatments that resulted in eradication included 75.5% (670/892) of human patients and 71.4% (150/210) of mice. Moreover, only 0.8% of those treated experienced re-infection after 2–4 months, 4.7% after 10–12 months, 0.1% after 2–7 weeks post-treatment, and 1.8% experienced a recurrence of infection without a defined timeframe. In a single case report, a new bacterial variant evolved that was sensitive to phage administration. 32
A decrease in bacterial load was reported in 29% of the articles (16/55); these included 35% of mice (66/189), 50% of Nile tilapia (30/60), and 42.7% (207/485) of human patients. Interestingly, in two preclinical studies, a decrease in bacterial load was reported for one group of mice and not for the other. In the first article, authors performed two stage preclinical study comparing four groups of mice.
These groups were treated with either phosphate buffered saline, antibiotic, phage, or combination of phage + antibiotic. In this first stage, bacterial loads decreased in both phage and phage + antibiotic groups. This was then followed by a second stage where only phage groups were compared with phage + antibiotic group. In this second stage, bacterial loads were significantly lower in phage + antibiotic group compared with phage-only group. 82
In the second article, only the group of mice that were given high concentrations of phage showed microbiological efficacy. 37 In one of the reported cases described in a case series, a single female patient experienced an increase in bacterial load after the first course of treatment; however, the bacterial load was not assessed at the end of the second course of phage therapy. 53
Improvement of clinical symptoms was reported in most human patients; 97% (>995/1026), with relapse in just over 1.7% (17/1026). It is worth noting that in the 2010 Letkiewicz trial that included 22 patients, all but 2 cases experienced substantial clinical improvements. 53 One was reported as “not possible to evaluate” whereas in the second patient, no change in intensity of symptoms after treatment was reported. 53 Another study reported significant improvements with a relapse afterward, without specifying the number of enrolled subjects. 28
In a single clinical trial, clinical improvements were observed, but statistical significance was not achieved. 59 In only one of the 55 studies, a 72-year-old female patient found phage therapy unhelpful. 78 A table containing only human subjects stratified by organisms reported, therapy type, route of administration, efficacy, and safety can be found in Table 3.
Human Subjects Sub-Group Results on Phage Therapy for Urinary Tract Infections
Tabulated data enumerating results from human case reports, case series, and clinical trials throughout the review period (until November 17, 2022). See Supplementary Table S5 for data extraction sheet.
Abx can include vaccine or toxoid therapy.
PO, oral administration.
In terms of phage resistance, 80% of the articles failed to specify its incidence. Two studies (3.6%) stated that no phage resistance was observed, whereas in the remaining studies (16.1% n = 9) phage resistance was reported. In the largest case series (n = 25) that reported the development of resistance, 21% of 90 isolates recovered following treatment had become resistant to phages. A further 4.3% were resistant to both the phages and antibiotics that were used for treatment. 80 In all instances, expanded phage susceptibility testing was not reported.
Safety of phage therapy
In most of the reported cases, phages were safe, with no reported adverse effects. While 58.1% of the articles failed to specify whether adverse effects were seen, 20 studies (36.3%) reported no adverse effects, and only 3 studies (5.45%) described adverse effects after phage administration. In the first study, one patient experienced a sudden fever and chills on the third day after phage administration, which was attributed to the pre-existing P. aeruginosa infection. 73
In another, the patient initially experienced an increase in testicular and back pain after starting treatment, but those symptoms subsided after three weeks. 46 Finally, in the third article, 21% of patients treated with phage therapy experienced adverse events: 4% were grade 1, 4% were grade 2, 11% were grades 3, and 4% were lost to follow-up. Of note, this was in comparison to 41% of the placebo group and 30% of the antibiotic group who experienced diverse effects in that same trial. 51
Critical appraisal of phage therapy studies
There was a total of 14 case reports included in our review, with 1 case report being marginally accepted following the critical appraisal. A total of 17 case series were assessed, with 6 case series being marginally accepted. Meanwhile, all four human RCTs were included. Critical appraisal summaries for case reports, case series, and human RCTs used in our analysis can be found in Table 3 and Supplementary Table S3 (case reports and case series), and Supplementary Table S4 (Human RCTs).
Discussion
In the past decade, there has been a resurgence of interest in phages and their potential to overcome antibiotic-resistant and chronic urinary tract-associated infections. This systematic review is intended to provide an overview of the extent, range, and nature of all available UTI phage therapy trials, and to synthesize data to help in the evaluation of phages as an option for control of UTIs. It is the first systematic review to assess phage therapy efficacy in UTIs without restrictions in terms of language or time frame.
We followed Cochrane methodology and PRISMA guidelines, ensuring that the review is comprehensive, reproducible, transparent, and with the goal of being unbiased. Following careful screening, we reviewed 55 articles that investigated the use of phages in humans and in animal models, including case studies, case reports, preclinical, RCTs, and non-randomized control clinical trials.
It is encouraging that more than half of the articles fulfilling our inclusion criteria (65.4%, 37/55) were published in the past 19 years, with a gap in publications from 1996 through 2005 (Fig. 3). This distribution reflects the recent increase in interest and experience in the use of phage therapy for UTIs.
The success rate of phage therapy was defined based on microbiological and clinical outcomes, and >72.7% of the included articles reported improvements following phage administration. However, of the 93 phage therapy studies covered by the 55 articles, all but 17 studies used concomitant treatments. These confounders make it harder to determine the explicit contribution of phages in treatment success.
Our systematic review reports fewer clinical improvements compared with another 17 that included a section on phage therapy in UTIs. The latter reported 100% clinical improvement in all included articles. This discrepancy may be due to differences in the number of articles included. We placed no restrictions on timeframe and language search, whereas the other systematic review included only English-language studies published between 2000 and 2021.
Analysis on phage therapy UTI data focusing on human subjects in greater detail is revealing. As seen in Table 3 and Supplementary Table S5, out of the roughly 1400 distinct patient applications or study arms (Patients may be used more than once in a subsequent arm), phages were used alone in 39% of cases, with antibiotics in 18% of cases, and not specified in 43% of applications. Moreover, the route of administration had a plurality of intravesicular (urinary bladder and rarely kidney pelvis) routes, with less occurrences of oral, or combination therapy.
Clinical efficacy when specified was 79% for marked improvement/cure, 15% for improvement, and no improvement in 6%; unfortunately, there was a high percentage of non-specified distinct applications, which was 35% of the 1450 study arms. Microbiological outcomes showed marked improvement and improvement in 67% and 14% of cases, respectively.
Of the 1089 evaluated applications or study arms, only on 54 occasions microbiology outcome was not specified. Lastly, no adverse events were indicated in 621 phage therapy patients (99% when specified) and in only eight situations did a patient report a mild adverse event (1% when specified). This was limited due to the high number of situations where adverse events were not specified: 56% over a total of 1432 occurrences.
Importantly, we identified and analyzed four recent articles reporting the results of RCTs using phage therapy to treat UTI, three of which were not included in prior analyses. The Dolgolikova et al. RCT 48 was a three-armed trial assessing recurrent UTI following kidney transplant. They showed that with standard of care, the average number of UTI recurrence in the following year was seven, in the phage therapy group combined with antibiotics the average yearly UTI recurrence was reduced to two, and in the group that received phage therapy with antibiotics and a probiotic solution, the recurrence rate was zero.
This is in keeping with other studies in this review that show increased efficacy with concurrent antibiotic administration. Kim et al. demonstrated in a Phase 1b RCT 27 that phage therapy can significantly decrease the concentration of E. coli recovered from the bladder in people who were known to be colonized. This work has now progressed to a large phase 2/3 trial for phage therapy in acute UTI. The Zaitsev et al. RCT 33 reported significant efficacy with bladder instillation of phage in women with recurrent UTI.
Microbiologic cure was reported after approximately two weeks from the start of therapy in most cases, and clinical improvement was monitored via symptom score questionnaires. However, not all of the RCTs show efficacy. An RCT using phage therapy for men with complicated UTI or recurrent uncomplicated UTI 51 demonstrated that placebo was superior to a phage therapy cocktail with in vitro efficacy against their isolates.
This was attributed to a therapeutic benefit from bladder irrigation regardless of lack of active treatment. Interestingly, the phage therapy cocktail was non-inferior to antibiotic standard of care, although both performed poorly as compared with placebo. Regardless of the efficacy results, none of the trials reported significant adverse events.
Understanding the safety considerations of phage therapies is crucial for their responsible and sustainable use. Collection of safety information ensures that phage-based therapies are effective and compliant with regulatory standards. In terms of safety, only 5.4% (3/55) of the included studies reported adverse events after phage administration. It is essential to carefully consider missing data and develop strategies to address any gaps in reporting, since 60% of the articles failed to specify adverse events.
From this review, we conclude that in most cases, phages were a successful treatment option and could potentially be used instead of, or as an adjuvant therapy with antibiotics. Bacteriophage therapy was effective both when a single-phage and a multi-phage cocktail was administered, although most studies failed to provide insight into potential phage resistance or associated adverse events. In conclusion, phages have been demonstrated to be effective in treating infections with negligible safety concerns, in agreement with other recent systematic reviews on phage therapy.17,83–85
Limitations
This systematic review has several limitations. First, our systematic review had high heterogeneity. We assessed results from many different types of UTIs and included articles from all years, languages, and animal systems. Further, we chose to retain studies in our analyses even if our assessment deemed them to be only marginally acceptable. Our comprehensive, historical approach was intentional, as this field has not been studied in detail.
However, this heterogeneity presented some challenges in drawing conclusions on the safety and efficacy of phage therapy and identifying whether there may be an optimal treatment strategy. Without consistent information presented in each study, we were restricted to descriptive analysis rather than statistical or meta-analyses. Despite these limitations, there was a promising trend for the success of phage therapy in treating UTIs. It should be acknowledged that investigators tend to publish only positive results (publication bias), which could affect the type and number of phage therapy studies available for analysis.
Moreover, systematic reviews without language restrictions have the inherent risk of translation and interpretation errors that may have impacted our analyses. To mitigate this effect, we used translation software that was recently validated for its high accuracy. 86 We feel the benefit of adding these data outweighs any challenges related to translation and interpretations.
In addition, The Joanna Briggs Institute cautions against using absolute scores for quality assessment of case series. 87 Therefore, we did not provide a numeric score for the studies. Due to the historical and comprehensive nature of this review, we elected to keep all results, regardless of their overall appraisal status.
Our team was multidisciplinary and composed of individuals with different levels of education, training, and expertise. Three of the authors are phage scientists, two are physicians, and one is an experienced reference librarian. One co-primary reviewer was consistent (P.B.H.) throughout the process, whereas the second co-primary reviewer changed three times (A.M.A., G.J.G., and J.D.C.) due to operational factors.
This may have led to inconsistencies. We attempted to limit this impact by ensuring each reviewer had training on our protocol before reviewing articles. Pilot studies were also done to ensure consistency and, our adjudicator, a phage scientist (A.P.H.), resolved the conflicts between various independent reviewers for each round of the article review process, except for the initial round of title and abstract screening and the critical appraisal (G.J.G.).
Future directions
Our findings suggest that phage therapy is safe and effective in treating UTIs in a variety of animal models and humans. Although there has been a recent increase in the number of studies using phage therapy for treating UTIs, the quality of these studies is variable. Thus, there is a need for researchers and clinicians to use standardized treatment, monitoring, and reporting protocols and, ideally, to share this information with a phage registry.
Recently, a process called the Standardised Treatment and Monitoring Protocol (STAMP) was approved in Australia for patients receiving phage therapy. 88 The Phage Australia group anticipates that results from clinical trials following the STAMP protocol will be more homogenous and provide stronger evidence of the safety and efficacy of phage therapy. We foresee that future systematic reviews on phage therapy for UTIs will have less heterogeneity, making quantitative analyses possible.
As far as we know, this is the largest systematic review for any single clinical indication treated with phage therapy. There were four other systematic reviews for different clinical sequelae, bone and joint infections (n = 20 and n = 17), superficial bacterial infections (n = 27), and chronically infected wounds infections (n = 13).83,89–91 We identified two other systematic reviews that evaluated phage therapy across multiple clinical syndromes, including UTIs.
Uttebroek et al.'s review included only human-based studies published in English after 2000. 17 Meanwhile, Gómez-Ochoa et al. employed a broader approach where they searched for animal-only studies published in any language, but their date range was limited to database inception, which was 1963. 84
Our lack of date, language, and research subject restrictions allowed us to capture relevant literature dating back to 1926 across four different languages since the use of phages for therapy predates the antibiotic era. 92 We recommend that systematic reviews evaluating phage therapy for other syndromes implement a similar search strategy encompassing all years and all languages to provide a global perspective in the field. This is particularly important, as more than 20% of the studies in our review were published in languages other than English.
We observed that phage therapy for UTIs in humans historically has a high success rate rivaling antibiotics of today, with few if any adverse events reported. We anticipate that the safety and efficacy demonstrated in our review may be useful in guiding the development of phage therapy clinical practice guidelines, treatment regimens, and dosing schedules. In addition, this review may serve as useful evidence supporting policymaking and research grant applications regarding phage therapy.
Conclusion
In this comprehensive systematic review, we analyzed reports on the safety and efficacy of phage therapy in UTIs and suggest that phage therapy can be a promising approach to treating UTIs caused by antibiotic-resistant bacteria. However, even recent studies have limitations, including small sample sizes, lack of randomized controlled trials, and limited data on the long-term effects of phage therapy.
Thus, larger well-designed clinical trials are warranted to establish the clinical effectiveness and safety of phage therapy for UTIs. While this review supports the potential of phage therapy as a valuable intervention for the treatment of UTIs, more research is needed to establish the long-term safety and efficacy of the therapy and to support its broader use.
Footnotes
Acknowledgments
L.L.B. holds a Tier 1 Canada Research Chair in Microbe-Surface Interactions. They would also like to thank Glyneva Bradley-Ridout, Liaison & Education Librarian at the University of Toronto Libraries, for peer reviewing the search strategy and providing feedback through the PRESS checklist. Finally, the authors thank Rachel Couban librarian at McMaster University for her guidance in the systematic review protocol preparation.
Authors' Contributions
A.M.A. and P.B.H. performed the systematic review. J.D.C. and P.B.H. performed the risk-of-bias assessment. A.P.H. and G.J.G. resolved conflicts during articles' inclusion assessment and data extraction. A.P.H., G.J.G., and J.D.C. participated in the process of article's selection. A.M.A. and P.B.H.: writing—original draft preparation; A.M.A., P.B.H., and J.D.C.: writing—review and editing. J.M. developed the search strategy. G.J.G. reviewed the manuscript and provided clinical expertise for the review. G.J.G. is the guarantor of the review; A.P.H. reviewed the manuscript, supervised, and provided resources; and L.L.B.: coordinated the Braley Fellows Program and edited the manuscript. All the authors read and approved the final manuscript.
Author Disclosure Statement
No competing financial interests exist.
Funding Information
The authors thank the David Braley Fellows program (David Braley Centre for Antibiotic Discovery), McMaster University and Laboratory Medicine Physician's of St. Michael's Hospital, Toronto for funding and sponsorship. A.P.H. acknowledges funding through the Natural Sciences and Engineering Council of Canada (NSERC) Discovery Grant 2018-05996 and the Farncombe Family Chair in Phage Biology.
References
Supplementary Material
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