Evidence map›Paper›PMID 29686284›Full record

ArticleNature communications2018

Multi-faceted immunomodulatory and tissue-tropic clinical bacterial isolate potentiates prostate cancer immunotherapy.

Jonathan F Anker, Anum F Naseem, Hanlin Mok, Anthony J Schaeffer, Sarki A Abdulkadir, Praveen Thumbikat

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 6% 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

64 citing papers in PubMed, 2 syntheses or guidelines pooled it, 104 citations in OpenAlex.

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4 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

6 authors at 1 institution in 1 country.

Jonathan F AnkerDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.ORCID http://orcid.org/0000-0002-2918-0346
Anum F NaseemDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
Hanlin MokDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
Anthony J SchaefferDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
Sarki A AbdulkadirDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA. Sarki.abdulkadir@northwestern.edu.
Praveen ThumbikatDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA. thumbikat@northwestern.edu.
Northwestern University · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Targeting FOXA1-downstream pathways: a novel therapeutic strategy for castration-resistant prostate cancerP50CA180995 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A., HUSSAIN, MAHA H · 2015 to 2025
$19.9M
Lipoteichoic acid mediated modulation of chronic painR01DK108127 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI THUMBIKAT, PRAVEEN · 2016 to 2025
$3.6M
Mast cells in male pelvic pain and lower urinary tract dysfunctionR01DK083609 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI THUMBIKAT, PRAVEEN · 2010 to 2020
$3.4M
Role of Oncogenic Kinase Pim-1 in Prostate CancerR01CA123484 · NCI · VANDERBILT UNIVERSITY · PI ABDULKADIR, SARKI A. · 2007 to 2017
$2.9M
Prostate Cancer Recurrence: models and mechanismsR01CA167966 · NCI · VANDERBILT UNIVERSITY · PI ABDULKADIR, SARKI A. · 2012 to 2016
$1.8M
T cells in Chronic Pelvic PainR01DK094898 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI THUMBIKAT, PRAVEEN · 2013 to 2016
$1.5M
Clinical bacterial isolate engineered as an immunotherapy for prostate cancerF30CA203472 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ANKER, JONATHAN FORREST · 2016 to 2019
$197k
NCI NIH HHS F30 CA203472NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA180995NCI NIH HHS R01 CA123484NCI NIH HHS R01 CA167966NIDDK NIH HHS R01 DK083609NIDDK NIH HHS R01 DK094898NIDDK NIH HHS R01 DK108127
6 · The paper itself

Abstract

Immune checkpoint inhibitors have not been effective for immunologically "cold" tumors, such as prostate cancer, which contain scarce tumor infiltrating lymphocytes. We hypothesized that select tissue-specific and immunostimulatory bacteria can potentiate these immunotherapies. Here we show that a patient-derived prostate-specific microbe, CP1, in combination with anti-PD-1 immunotherapy, increases survival and decreases tumor burden in orthotopic MYC- and PTEN-mutant prostate cancer models. CP1 administered intra-urethrally specifically homes to and colonizes tumors without causing any systemic toxicities. CP1 increases immunogenic cell death of cancer cells, T cell cytotoxicity, and tumor infiltration by activated CD8 T cells, Th17 T cells, mature dendritic cells, M1 macrophages, and NK cells. CP1 also decreases intra-tumoral regulatory T cells and VEGF. Mechanistically, blocking CP1-recruited T cells from infiltrating the tumor inhibits its therapeutic efficacy. CP1 is an immunotherapeutic tool demonstrating how a tissue-specific microbe can increase tumor immunogenicity and sensitize an otherwise resistant cancer type to immunotherapy.

Indexed as

AnimalsCell Line, TumorDrug Resistance, NeoplasmHEK293 CellsHumansImmunotherapyInjections, IntralesionalLymphocyte ActivationLymphocytes, Tumor-InfiltratingMaleMiceMice, KnockoutProgrammed Cell Death 1 ReceptorProstateProstatic NeoplasmsProstatitisPDCD1 protein, humanProgrammed Cell Death 1 ReceptorPTEN PhosphohydrolasePten protein, mouse

Identifiers

PMID29686284
PMCPMC5913311
OpenAlexW2802262365

What OpenQuestion holds

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LicenceCC BY
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.