Evidence map›Paper›PMID 32680964›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Bacterial immunotherapy for cancer induces CD4-dependent tumor-specific immunity through tumor-intrinsic interferon-γ signaling.

Anthony C Antonelli, Anna Binyamin, Tobias M Hohl, Michael S Glickman, Gil Redelman-Sidi

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% of its field
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

69 citing papers in PubMed, 1 synthesis or guideline pooled it, 99 citations in OpenAlex.

  1. Pooled it
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  18. Bacterial live therapeutics for human diseases.Molecular systems biology · 2024
    Review
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  20. Review

9 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Anthony C AntonelliImmunology and Microbial Pathogenesis, Weill Cornell Medicine Graduate School of Medical Sciences, New York, NY 10065.ORCID 0000-0002-0775-4468
Anna BinyaminImmunology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065.ORCID 0000-0001-6159-6440
Tobias M HohlImmunology and Microbial Pathogenesis, Weill Cornell Medicine Graduate School of Medical Sciences, New York, NY 10065.ORCID 0000-0002-9097-5412
Michael S GlickmanImmunology and Microbial Pathogenesis, Weill Cornell Medicine Graduate School of Medical Sciences, New York, NY 10065; glickmam@mskcc.org redelmag@mskcc.org.ORCID 0000-0001-7918-5164
Gil Redelman-SidiDivision of Infectious Diseases, Memorial Sloan Kettering Cancer Center, New York, NY 10021 glickmam@mskcc.org redelmag@mskcc.org.ORCID 0000-0002-8841-777X
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
SPORE in Bladder CancerP50CA221745 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI BAJORIN, DEAN F. · 2018 to 2024
$11.8M
INITIATION OF THE IMMUNE RESPONSE TO ASPERGILLUS FUMIGATUSR01AI093808 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI HOHL, TOBIAS M · 2011 to 2020
$4.9M
BCG therapy of bladder cancer: the role of BCG uptake by bladder cancer cellsK08CA184038 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI REDELMAN-SIDI, GIL · 2014 to 2018
$839k
Immunology and Microbial Pathogenesis Research Training ProgramT32AI134632 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI EHRT, SABINE, LI, MING · 2019 to 2023
$747k
NCI NIH HHS K08 CA184038NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA221745NIAID NIH HHS R01 AI093808NIAID NIH HHS T32 AI134632
6 · The paper itself

Abstract

Bacillus Calmette-Guérin (BCG) immunotherapy for bladder cancer is the only bacterial cancer therapy approved for clinical use. Although presumed to induce T cell-mediated immunity, whether tumor elimination depends on bacteria-specific or tumor-specific immunity is unknown. Herein we show that BCG-induced bladder tumor elimination requires CD4 and CD8 T cells, although augmentation or inhibition of bacterial antigen-specific T cell responses does not alter the efficacy of BCG-induced tumor elimination. In contrast, BCG stimulates long-term tumor-specific immunity that primarily depends on CD4 T cells. We demonstrate that BCG therapy results in enhanced effector function of tumor-specific CD4 T cells, mainly through enhanced production of IFN-γ. Accordingly, BCG-induced tumor elimination and tumor-specific immune memory require tumor cell expression of the IFN-γ receptor, but not MHC class II. Our findings establish that a bacterial immunotherapy for cancer is capable of inducing tumor immunity, an antitumor effect that results from enhanced function of tumor-specific CD4 T cells, and ultimately requires tumor-intrinsic IFN-γ signaling, via a mechanism that is distinct from other tumor immunotherapies.

Indexed as

Urinary Bladder NeoplasmsAnimalsAntineoplastic AgentsBCG VaccineCD4-Positive T-LymphocytesCell Line, TumorHumansImmunotherapyInterferon-gammaMiceNeoplasms, ExperimentalAntineoplastic AgentsBCG VaccineInterferon-gammaBCGbladder cancerimmunotherapyT celltumor immunity

Identifiers

PMID32680964
PMCPMC7414065
OpenAlexW3042421025

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.