Evidence map›Paper›PMID 42032071›Full record

ArticleNature medicine2026

Cross-reactive anti-prophage antibodies and bacterial heteroresistance implicated in phage therapeutic failure.

F Gordillo Altamirano, D Subedi, M Beiers, M Bucher, S Dahlman, D M Patel, M Parker, D Korneev, M J Robinson, K Pragastis and 11 more

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Nature medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Vancomycin and phage COP-80B combination therapy for Staphylococcus epidermidis periprosthetic joint infections: a preclinical mouse study.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

F Gordillo AltamiranoDepartment of Infectious Diseases, Alfred Care Group and School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-4581-1259
D SubediCentre to Impact AMR, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-1357-9520
M BeiersDepartment of Infectious Diseases, Alfred Care Group and School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
M BucherSchool of Biological Sciences, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0009-0005-1296-6288
S DahlmanSchool of Biological Sciences, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0009-0009-9723-1705
D M PatelAntibody Discovery Platform, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-0375-2318
M ParkerDepartment of Infectious Diseases, Alfred Care Group and School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
D KorneevRamaciotti Centre for Cryo-Electron Microscopy, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0003-4350-8317
M J RobinsonDepartment of Immunology, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0001-5677-3078
K PragastisDepartment of Infectious Diseases, Alfred Care Group and School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
J WisniewskiDepartment of Infectious Diseases, Alfred Care Group and School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
C ReesMelbourne Water Corporation, Melbourne, Victoria, Australia.
H RamshawAntibody Discovery Platform, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0001-9909-282X
S F KhanDepartment of Infectious Diseases, Alfred Care Group and School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-1882-7423
B J GardinerDepartment of Infectious Diseases, Alfred Care Group and School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0001-5609-3937
Y HammerschlagDepartment of Infectious Diseases, Alfred Care Group and School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
D KeatingDepartment of Respiratory Medicine, Alfred Care Group, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0001-6150-6927
T KotsimbosDepartment of Respiratory Medicine, Alfred Care Group, Melbourne, Victoria, Australia.
J HawkeyDepartment of Infectious Diseases, Alfred Care Group and School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0001-9661-5293
J J BarrCentre to Impact AMR, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0001-5603-5294
A Y PelegDepartment of Infectious Diseases, Alfred Care Group and School of Translational Medicine, Monash University, Melbourne, Victoria, Australia. anton.peleg@monash.edu.ORCID http://orcid.org/0000-0002-2296-2126

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phage therapy is an exciting strategy against antimicrobial-resistant bacterial infections, but critical knowledge gaps regarding its clinical application persist. Here we present a case study of a 22-year-old male patient with cystic fibrosis, presenting with a recurrent, invasive and ultimately lethal Bordetella bronchialis infection, who failed compassionate-use phage therapy. Using longitudinal clinical samples, we found that our patient harbored pre-existing antibodies against active prophages induced from the genome of the infecting pathogen. Notably, these antibodies may have contributed to clinical failure by cross-reacting with and effectively neutralizing therapeutic phage. We also uncovered bacterial heteroresistance, characterized by bacterial subpopulations from the initial infection with reduced phage susceptibility, as a possible further contributor to treatment failure. These findings highlight the intricate interplay between host immunology, bacterial genetic diversity and phage biology, bearing broad importance for clinical phage therapy. Future phage therapy patients, especially those with chronic infections, should be screened for antiphage immunity and bacterial heteroresistance before phage treatment.

Indexed as

Antibodies, ViralBordetella bronchisepticaBordetella InfectionsPhage TherapyProphagesCross ReactionsHumansMaleTreatment FailureYoung AdultAntibodies, Viral

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.