TY - JOUR
T1 - Bacteriophage therapy for difficult-to-treat infections
T2 - The implementation of a multidisciplinary phage task force (the phageforce study protocol)
AU - Onsea, Jolien
AU - Uyttebroek, Saartje
AU - Chen, Baixing
AU - Wagemans, Jeroen
AU - Lood, Cédric
AU - Van Gerven, Laura
AU - Spriet, Isabel
AU - Devolder, David
AU - Debaveye, Yves
AU - Depypere, Melissa
AU - Dupont, Lieven
AU - De Munter, Paul
AU - Peetermans, Willy E.
AU - van Noort, Vera
AU - Merabishvili, Maia
AU - Pirnay, Jean Paul
AU - Lavigne, Rob
AU - Metsemakers, Willem Jan
N1 - Publisher Copyright:
© 2021 by the authors.
PY - 2021/8
Y1 - 2021/8
N2 - 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.
AB - 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.
KW - Bacteriophage therapy
KW - Difficult-to-treat infections
KW - Efficacy
KW - Patient registry
KW - Safety
UR - http://www.scopus.com/inward/record.url?scp=85112160123&partnerID=8YFLogxK
U2 - 10.3390/v13081543
DO - 10.3390/v13081543
M3 - Article
C2 - 34452408
AN - SCOPUS:85112160123
SN - 1999-4915
VL - 13
JO - Viruses
JF - Viruses
IS - 8
M1 - 1543
ER -