Bacteriophage Therapy for Difficult-to-Treat Infections: The Implementation of a Multidisciplinary Phage Task Force (<i>The PHAGEFORCE Study Protocol</i>)
Jolien Onsea,
Saartje Uyttebroek,
Baixing Chen,
Jeroen Wagemans,
Cédric Lood,
Laura Van Gerven,
Isabel Spriet,
David Devolder,
Yves Debaveye,
Melissa Depypere,
Lieven Dupont,
Paul De Munter,
Willy E. Peetermans,
Vera van Noort,
Maia Merabishvili,
Jean-Paul Pirnay,
Rob Lavigne,
Willem-Jan Metsemakers
Affiliations
Jolien Onsea
Department of Trauma Surgery, University Hospitals Leuven, 3000 Leuven, Belgium
Saartje Uyttebroek
Department of Otorhinolaryngology, University Hospitals Leuven, 3000 Leuven, Belgium
Baixing Chen
Department of Trauma Surgery, University Hospitals Leuven, 3000 Leuven, Belgium
Jeroen Wagemans
Department of Biosystems, Laboratory of Gene Technology, KU Leuven, 3000 Leuven, Belgium
Cédric Lood
Department of Biosystems, Laboratory of Gene Technology, KU Leuven, 3000 Leuven, Belgium
Laura Van Gerven
Department of Otorhinolaryngology, University Hospitals Leuven, 3000 Leuven, Belgium
Isabel Spriet
Pharmacy Department, University Hospitals Leuven, 3000 Leuven, Belgium
David Devolder
Pharmacy Department, University Hospitals Leuven, 3000 Leuven, Belgium
Yves Debaveye
Department of Intensive Care Medicine, University Hospitals Leuven, 3000 Leuven, Belgium
Melissa Depypere
Department of Laboratory Medicine, University Hospitals Leuven, 3000 Leuven, Belgium
Lieven Dupont
Department of Pneumology, University Hospitals Leuven, 3000 Leuven, Belgium
Paul De Munter
Department of Internal Medicine, University Hospitals Leuven, 3000 Leuven, Belgium
Willy E. Peetermans
Department of Internal Medicine, University Hospitals Leuven, 3000 Leuven, Belgium
Vera van Noort
Center of Microbial and Plant Genetics, KU Leuven, 3000 Leuven, Belgium
Maia Merabishvili
Laboratory for Molecular and Cellular Technology, Queen Astrid Military Hospital, 1120 Brussels, Belgium
Jean-Paul Pirnay
Laboratory for Molecular and Cellular Technology, Queen Astrid Military Hospital, 1120 Brussels, Belgium
Rob Lavigne
Department of Biosystems, Laboratory of Gene Technology, KU Leuven, 3000 Leuven, Belgium
Willem-Jan Metsemakers
Department of Trauma Surgery, University Hospitals Leuven, 3000 Leuven, Belgium
In times where only a few novel antibiotics are to be expected, antimicrobial resistance remains an expanding global health threat. In case of chronic infections caused by therapy-resistant pathogens, physicians have limited therapeutic options, which are often associated with detrimental consequences for the patient. This has resulted in a renewed interest in alternative strategies, such as bacteriophage (phage) therapy. However, there are still important hurdles that currently impede the more widespread implementation of phage therapy in clinical practice. First, the limited number of good-quality case series and clinical trials have failed to show the optimal application protocol in terms of route of administration, frequency of administration, treatment duration and phage titer. Second, there is limited information on the systemic effects of phage therapy. Finally, in the past, phage therapy has been applied intuitively in terms of the selection of phages and their combination as parts of phage cocktails. This has led to an enormous heterogeneity in previously published studies, resulting in a lack of reliable safety and efficacy data for phage therapy. We hereby present a study protocol that addresses these scientific hurdles using a multidisciplinary approach, bringing together the experience of clinical, pharmaceutical and molecular microbiology experts.