Evidence map›Paper›PMID 39423284›Full record

ArticleScience immunology2024

Programmable bacteria synergize with PD-1 blockade to overcome cancer cell-intrinsic immune resistance mechanisms.

Fangda Li, Zaofeng Yang, Thomas M Savage, Rosa L Vincent, Kenia de Los Santos-Alexis, Alexander Ahn, Mathieu Rouanne, Dylan L Mariuzza, Tal Danino, Nicholas Arpaia

Abstract read
In one paragraph

Article in Science immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Review
  2. BiohybridMaterials today. Bio · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Therapeutic bacteria-trained NK cells confer long-term protection against cancer metastasis.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  8. Article
  9. Living Microbial Drugs.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Microbiome Modulation withJournal of microbiology and biotechnology · 2026
    Article
  16. Review
  17. Review
  18. Article
  19. Natural and Engineered Cytokines as Cancer Therapeutics.Annual review of cancer biology · 2026
    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

10 authors.

Fangda LiDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.ORCID 0000-0002-4697-3989
Zaofeng YangDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.ORCID 0000-0003-4861-9729
Thomas M SavageDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.ORCID 0000-0002-6618-2973
Rosa L VincentDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.ORCID 0000-0003-0742-8977
Kenia de Los Santos-AlexisDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.ORCID 0000-0002-3628-9796
Alexander AhnDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.ORCID 0000-0003-4868-3149
Mathieu RouanneDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.ORCID 0000-0003-2970-4821
Dylan L MariuzzaDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.ORCID 0000-0002-9369-2514
Tal DaninoDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.ORCID 0000-0003-2713-7659
Nicholas ArpaiaDepartment of Microbiology and Immunology, Columbia University, New York, NY, USA.ORCID 0000-0002-0657-0528

Funding

Modulation of the tumor microenvironment with probiotic therapiesR01CA249160 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI ARPAIA, NICHOLAS, DANINO, TAL · 2020 to 2024
$3.0M
Treating colon cancer by regulating intestinal immunity through microbial metabolismR01CA259634 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ARPAIA, NICHOLAS · 2021 to 2025
$2.8M
NCI NIH HHS R01 CA249160NCI NIH HHS R01 CA259634
6 · The paper itself

Abstract

Interferon-γ (IFN-γ) is a potent cytokine critical for response to immunotherapy, yet conventional methods to systemically deliver this cytokine have been hindered by severe dose-limiting toxicities. Here, we engineered a strain of probiotic bacteria that home to tumors and locally release IFN-γ. A single intratumoral injection of these IFN-γ-producing bacteria was sufficient to drive systemic tumor antigen-specific antitumor immunity, without observable toxicity. Although cancer cells use various resistance mechanisms to evade immune responses, bacteria-derived IFN-γ overcame primary resistance to programmed cell death 1 (PD-1) blockade via activation of cytotoxic Foxp3

Indexed as

Immune Checkpoint InhibitorsNeoplasmsProgrammed Cell Death 1 ReceptorAnimalsCell Line, TumorFemaleHumansImmunotherapyInterferon-gammaMiceMice, Inbred C57BLImmune Checkpoint InhibitorsInterferon-gammaProgrammed Cell Death 1 Receptor

Identifiers

PMID39423284
PMCPMC11984541

What OpenQuestion holds

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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.