Evidence map›Paper›PMID 32324171›Full record

ArticleJCI insight2020

Commensal bacteria stimulate antitumor responses via T cell cross-reactivity.

Catherine A Bessell, Ariel Isser, Jonathan J Havel, Sangyun Lee, David R Bell, John W Hickey, Worarat Chaisawangwong, Joan Glick Bieler, Raghvendra Srivastava, Fengshen Kuo and 4 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% 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

112 citing papers in PubMed, 1 synthesis or guideline pooled it, 167 citations in OpenAlex.

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52 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

14 authors at 4 institutions in 1 country.

Catherine A BessellGraduate Program in Immunology and.
Ariel IsserDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland, USA.
Jonathan J HavelHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Sangyun LeeComputational Biology Center, IBM Thomas J. Watson Research Center, Yorktown Heights, New York, USA.
David R BellComputational Biology Center, IBM Thomas J. Watson Research Center, Yorktown Heights, New York, USA.
John W HickeyDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland, USA.
Worarat ChaisawangwongDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Joan Glick BielerDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Raghvendra SrivastavaHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Fengshen KuoHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Tanaya PurohitHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Ruhong ZhouComputational Biology Center, IBM Thomas J. Watson Research Center, Yorktown Heights, New York, USA.
Timothy A ChanHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Jonathan P SchneckGraduate Program in Immunology and.
Johns Hopkins University · USMemorial Sloan Kettering Cancer Center · USIBM Research - Thomas J. Watson Research Center · USCleveland Clinic · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
TR&D Project 3P41EB028239 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI Jordan Green, JONATHAN P SCHNECK · 2019 to 2026
$11.5M
BIOMEDICAL ENGINEERING TRAINING PROGRAMT32GM007057 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI KANOLD, PATRICK O, KARCHIN, RACHEL · 1985 to 2023
$10.4M
TOWARDS PRECISION IMMUNO-ONCOLOGY: UNRAVELING THE GENOMIC DETERMINANTS AND MECHANISMS UNDERLYING IMMUNOTHERAPY EFFICACY AND RESISTANCER35CA232097 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CHAN, TIMOTHY AN-THY · 2018 to 2024
$7.0M
Use of aAPC for Melanoma Adoptive ImmunotherapyR01CA108835 · NCI · JOHNS HOPKINS UNIVERSITY · PI SCHNECK, JONATHAN P · 2004 to 2015
$3.3M
Elucidating genetics of response to immune checkpoint blockade in lung cancerR01CA205426 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHAN, TIMOTHY AN-THY · 2017 to 2021
$3.2M
Translational Research in Oncology Training ProgramT32CA160001 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SAWYERS, CHARLES L. · 2011 to 2020
$2.0M
A high-throughput nanoparticle assay to characterize cancer neoepitope-specific T cellsR33CA229042 · NCI · JOHNS HOPKINS UNIVERSITY · PI SCHNECK, JONATHAN P · 2019 to 2021
$1.4M
Immunoswitch: A novel nanoparticle-based approach to immunotherapyR21EB023411 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI SCHNECK, JONATHAN P · 2018 to 2019
$450k
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA108835NCI NIH HHS R01 CA205426NCI NIH HHS R33 CA229042NCI NIH HHS R35 CA232097NCI NIH HHS T32 CA160001NIBIB NIH HHS P41 EB028239NIBIB NIH HHS R21 EB023411NIGMS NIH HHS T32 GM007057
6 · The paper itself

Abstract

Recent studies show gut microbiota modulate antitumor immune responses; one proposed mechanism is cross-reactivity between antigens expressed in commensal bacteria and neoepitopes. We found that T cells targeting an epitope called SVYRYYGL (SVY), expressed in the commensal bacterium Bifidobacterium breve (B. breve), cross-react with a model neoantigen, SIYRYYGL (SIY). Mice lacking B. breve had decreased SVY-reactive T cells compared with B. breve-colonized mice, and the T cell response was transferable by SVY immunization or by cohousing mice without Bifidobacterium with ones colonized with Bifidobacterium. Tumors expressing the model SIY neoantigen also grew faster in mice lacking B. breve compared with Bifidobacterium-colonized animals. B. breve colonization also shaped the SVY-reactive TCR repertoire. Finally, SVY-specific T cells recognized SIY-expressing melanomas in vivo and led to decreased tumor growth and extended survival. Our work demonstrates that commensal bacteria can stimulate antitumor immune responses via cross-reactivity and how bacterial antigens affect the T cell landscape.

Indexed as

AnimalsAntigens, NeoplasmBifidobacterium breveCross ReactionsEpitopes, T-LymphocyteGastrointestinal MicrobiomeMelanoma, ExperimentalMiceT-LymphocytesAntigens, NeoplasmEpitopes, T-LymphocyteAntigenCancer immunotherapyImmunologyOncologyT cells

Identifiers

PMID32324171
PMCPMC7205429
OpenAlexW3017739100

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.