Evidence map›Paper›PMID 40555239›Full record

ArticleImmunity2025

A fungal-derived adjuvant amplifies the antitumoral potency of Bacillus Calmette-Guérin via reprogramming granulopoiesis.

Leonardo F Jurado, Andrew W Daman, Ziyi Li, Vanessa M S Ross, Kristina Nikolaou, Kim A Tran, Oleg Loutochin, Victor A McPherson, Renaud Prével, Raquel Tarancón and 11 more

Abstract read
In one paragraph

Article in Immunity, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Route of BCG administration determines success.Human vaccines & immunotherapeutics · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. BCG HSP70 Reprograms Macrophages via Central Trained Immunity to Suppress Prostate Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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.

Leonardo F JuradoDepartment of Pathology, Department of Microbiology & Immunology, Department of Medicine, McGill International TB Centre, Meakins-Christie Laboratories, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Andrew W DamanDepartment of Pathology and Laboratory Medicine, Division of Cell and Cancer Biology, and Immunology & Microbial Pathogenesis Program, Weill Cornell Medicine Graduate School of Medical Sciences, New York, NY, USA.
Ziyi LiDepartment of Pharmacology & Therapeutics, McGill University, Montreal, QC, Canada.
Vanessa M S RossDepartment of Pathology, Department of Microbiology & Immunology, Department of Medicine, McGill International TB Centre, Meakins-Christie Laboratories, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Kristina NikolaouDepartment of Pathology, Department of Microbiology & Immunology, Department of Medicine, McGill International TB Centre, Meakins-Christie Laboratories, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Kim A TranDepartment of Pathology, Department of Microbiology & Immunology, Department of Medicine, McGill International TB Centre, Meakins-Christie Laboratories, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Oleg LoutochinDepartment of Urology, Jewish General Hospital, McGill University, Montreal, QC, Canada.
Victor A McPhersonDepartment of Urology, Jewish General Hospital, McGill University, Montreal, QC, Canada.
Renaud PrévelDepartment of Pathology, Department of Microbiology & Immunology, Department of Medicine, McGill International TB Centre, Meakins-Christie Laboratories, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Raquel TarancónDepartment of Pathology, Department of Microbiology & Immunology, Department of Medicine, McGill International TB Centre, Meakins-Christie Laboratories, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Katalina CoutoDepartment of Pharmacology & Therapeutics, McGill University, Montreal, QC, Canada.
Erwan PernetDepartment of Pathology, Department of Microbiology & Immunology, Department of Medicine, McGill International TB Centre, Meakins-Christie Laboratories, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Nargis KhanDepartment of Pathology, Department of Microbiology & Immunology, Department of Medicine, McGill International TB Centre, Meakins-Christie Laboratories, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Jin-Gyu CheongDepartment of Pathology and Laboratory Medicine, Division of Cell and Cancer Biology, and Immunology & Microbial Pathogenesis Program, Weill Cornell Medicine Graduate School of Medical Sciences, New York, NY, USA.
Reshma RamaiahDepartment of Pathology and Laboratory Medicine, Division of Cell and Cancer Biology, and Immunology & Microbial Pathogenesis Program, Weill Cornell Medicine Graduate School of Medical Sciences, New York, NY, USA.
Mythili KetavarapuDepartment of Pathology and Laboratory Medicine, Division of Cell and Cancer Biology, and Immunology & Microbial Pathogenesis Program, Weill Cornell Medicine Graduate School of Medical Sciences, New York, NY, USA.
Eva KaufmannDepartment of Pathology, Department of Microbiology & Immunology, Department of Medicine, McGill International TB Centre, Meakins-Christie Laboratories, McGill University Health Centre, McGill University, Montreal, QC, Canada.
Michael S GlickmanImmunology Program, Division of Infectious Diseases, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Ajitha ThanabalasuriarDepartment of Pharmacology & Therapeutics, McGill University, Montreal, QC, Canada.
Steven Z JosefowiczDepartment of Pathology and Laboratory Medicine, Division of Cell and Cancer Biology, and Immunology & Microbial Pathogenesis Program, Weill Cornell Medicine Graduate School of Medical Sciences, New York, NY, USA.
Maziar DivangahiDepartment of Pathology, Department of Microbiology & Immunology, Department of Medicine, McGill International TB Centre, Meakins-Christie Laboratories, McGill University Health Centre, McGill University, Montreal, QC, Canada. Electronic address: maziar.divangahi@mcgill.ca.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Histone Variant H3.3 as a Transcription Rheostat in the Immune SystemR01AI148416 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI Steven Zvi Josefowicz · 2020 to 2026
$4.6M
Next-Gen Oncopathology ProgramT32CA260293 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI Ethel Cesarman, BENJAMIN MONTEVERDE KLEAVELAND · 2022 to 2026
$1.4M
Immunology and Microbial Pathogenesis Research Training ProgramT32AI134632 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI EHRT, SABINE, LI, MING · 2019 to 2023
$747k
Writing and Interpreting the Chromatin Enhancer Code in Myeloid CellsF32GM100616 · NIGMS · ROCKEFELLER UNIVERSITY · PI JOSEFOWICZ, STEVEN ZVI · 2012 to 2014
$156k
Describing the Epigenetic Mechanisms in Control of Hematopoietic Development and Rapid Inflammatory ResponsesF31HL152706 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI DAMAN, ANDREW · 2021 to 2023
$140k
NCI NIH HHS P30 CA008748NCI NIH HHS T32 CA260293NHLBI NIH HHS F31 HL152706NIAID NIH HHS R01 AI148416NIAID NIH HHS T32 AI134632NIGMS NIH HHS F32 GM100616
6 · The paper itself

Abstract

In patients with non-muscle invasive bladder cancer, the standard immunotherapy involves intravesical Bacillus Calmette-Guérin (BCG). However, its success requires repeated doses, and ∼50% of patients do not benefit. Using a preclinical orthotopic bladder cancer model, we found that a single intravesical dose of combined BCG and β-glucan immunotherapy eradicated aggressive tumors, resulting in 100% survival. Through single-cell transcriptomic/epigenomic analysis, flow cytometry, and intravital imaging, we show that BCG and β-glucan reprogrammed hematopoietic stem and progenitor cells with imprinting in innate immune cells, particularly neutrophils. Reprogrammed neutrophils exhibited increased reactive oxygen species (ROS) production and infiltration into the tumor core, reducing tumor vascularization and growth. The tumor microenvironment can convert neutrophils into protumor cells; BCG and β-glucan prevented this conversion, promoting sustained antitumoral activity. These findings support β-glucan as a safe, effective adjuvant to enhance BCG immunotherapy in bladder cancer and other solid tumors.

Indexed as

Adjuvants, ImmunologicBCG Vaccinebeta-GlucansMycobacterium bovisNeutrophilsUrinary Bladder NeoplasmsAnimalsCell Line, TumorFemaleHematopoietic Stem CellsHumansImmunotherapyMiceMice, Inbred C57BLReactive Oxygen SpeciesTumor MicroenvironmentAdjuvants, ImmunologicBCG Vaccinebeta-GlucansReactive Oxygen SpeciesBCGbladder cancergranulopoiesisimmunotherapyinnate immune memorymelanomaneutrophilstrained immunityβ-glucan

Identifiers

PMID40555239
PMCPMC13480675

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.