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Clinical Research and Public HealthIn-Press PreviewInfectious diseaseVirology Open Access | 10.1172/jci.insight.209406

A review of published personalized phage therapy cases in clinical practice

Patrick M. Blankenberg,1 Robert Targ,1 Grace D. Cullen,1 Gina A. Suh,2 Krystyna Dąbrowska,3 Aarav Singh,4 Tiffany Luong,1 Daisuke Furukawa,1 and Paul L. Bollyky1

1Division of Infectious Diseases and Geographic Medicine, Department of Medi, Stanford University, Stanford, United States of America

2Division of Public Health, Infectious Diseases, and Occupational Medicine, , Mayo Clinic, Rochester, United States of America

3Laboratory of Phage Molecular Biology, Hirszfeld Institute of Immunology an, Polish Academy of Sciences, Wroclaw, Poland

4Department of Computational Biology, UCLA, Los Angeles, United States of America

Find articles by Blankenberg, P. in: PubMed | Google Scholar

1Division of Infectious Diseases and Geographic Medicine, Department of Medi, Stanford University, Stanford, United States of America

2Division of Public Health, Infectious Diseases, and Occupational Medicine, , Mayo Clinic, Rochester, United States of America

3Laboratory of Phage Molecular Biology, Hirszfeld Institute of Immunology an, Polish Academy of Sciences, Wroclaw, Poland

4Department of Computational Biology, UCLA, Los Angeles, United States of America

Find articles by Targ, R. in: PubMed | Google Scholar

1Division of Infectious Diseases and Geographic Medicine, Department of Medi, Stanford University, Stanford, United States of America

2Division of Public Health, Infectious Diseases, and Occupational Medicine, , Mayo Clinic, Rochester, United States of America

3Laboratory of Phage Molecular Biology, Hirszfeld Institute of Immunology an, Polish Academy of Sciences, Wroclaw, Poland

4Department of Computational Biology, UCLA, Los Angeles, United States of America

Find articles by Cullen, G. in: PubMed | Google Scholar |

1Division of Infectious Diseases and Geographic Medicine, Department of Medi, Stanford University, Stanford, United States of America

2Division of Public Health, Infectious Diseases, and Occupational Medicine, , Mayo Clinic, Rochester, United States of America

3Laboratory of Phage Molecular Biology, Hirszfeld Institute of Immunology an, Polish Academy of Sciences, Wroclaw, Poland

4Department of Computational Biology, UCLA, Los Angeles, United States of America

Find articles by Suh, G. in: PubMed | Google Scholar

1Division of Infectious Diseases and Geographic Medicine, Department of Medi, Stanford University, Stanford, United States of America

2Division of Public Health, Infectious Diseases, and Occupational Medicine, , Mayo Clinic, Rochester, United States of America

3Laboratory of Phage Molecular Biology, Hirszfeld Institute of Immunology an, Polish Academy of Sciences, Wroclaw, Poland

4Department of Computational Biology, UCLA, Los Angeles, United States of America

Find articles by Dąbrowska, K. in: PubMed | Google Scholar |

1Division of Infectious Diseases and Geographic Medicine, Department of Medi, Stanford University, Stanford, United States of America

2Division of Public Health, Infectious Diseases, and Occupational Medicine, , Mayo Clinic, Rochester, United States of America

3Laboratory of Phage Molecular Biology, Hirszfeld Institute of Immunology an, Polish Academy of Sciences, Wroclaw, Poland

4Department of Computational Biology, UCLA, Los Angeles, United States of America

Find articles by Singh, A. in: PubMed | Google Scholar

1Division of Infectious Diseases and Geographic Medicine, Department of Medi, Stanford University, Stanford, United States of America

2Division of Public Health, Infectious Diseases, and Occupational Medicine, , Mayo Clinic, Rochester, United States of America

3Laboratory of Phage Molecular Biology, Hirszfeld Institute of Immunology an, Polish Academy of Sciences, Wroclaw, Poland

4Department of Computational Biology, UCLA, Los Angeles, United States of America

Find articles by Luong, T. in: PubMed | Google Scholar |

1Division of Infectious Diseases and Geographic Medicine, Department of Medi, Stanford University, Stanford, United States of America

2Division of Public Health, Infectious Diseases, and Occupational Medicine, , Mayo Clinic, Rochester, United States of America

3Laboratory of Phage Molecular Biology, Hirszfeld Institute of Immunology an, Polish Academy of Sciences, Wroclaw, Poland

4Department of Computational Biology, UCLA, Los Angeles, United States of America

Find articles by Furukawa, D. in: PubMed | Google Scholar

1Division of Infectious Diseases and Geographic Medicine, Department of Medi, Stanford University, Stanford, United States of America

2Division of Public Health, Infectious Diseases, and Occupational Medicine, , Mayo Clinic, Rochester, United States of America

3Laboratory of Phage Molecular Biology, Hirszfeld Institute of Immunology an, Polish Academy of Sciences, Wroclaw, Poland

4Department of Computational Biology, UCLA, Los Angeles, United States of America

Find articles by Bollyky, P. in: PubMed | Google Scholar

Published October 27, 2026 - More info

JCI Insight. https://doi.org/10.1172/jci.insight.209406.
Copyright © 2026, Blankenberg et al. This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Published October 27, 2026 - Version history
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Abstract

The increase in antimicrobial resistant infections has fueled a resurgent interest in bacteriophage (phage) therapy. We conducted a literature review of personalized phage therapy cases in the peer-reviewed, English-language literature reported between 1/1/2005, to 8/31/2025 for which individual patient data were available, identifying and synthesizing data from a total of 323 patients described in 83 studies. Most patients (68%, 221/323) were treated with ≥ 2 phages (a phage cocktail). The median concentration of phages was 108 PFU/mL (IQR 107–109). Most patients (76%, 246/323) received antibiotics concurrent with phage therapy. The median duration of therapy was 10 days (IQR 5–21). The most common indications for phage therapy were skin/soft tissue, pulmonary, orthopedic, osteoarticular, and genitourinary infections. 144 patients received fixed (off-the-shelf) phage preparations whereas 179 received bespoke phage preparations (i.e., personalized therapy). For cases where outcomes data were available, 78% (253/323), experienced clinical improvement while the targeted pathogen was eradicated in 61% (177/290) of cases. Nine patients had treatment withdrawn due to tolerability concerns. These data indicate that there is substantial heterogeneity in current personalized phage therapy clinical practices but that this approach can be successful.

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