Evidence map›Paper›PMID 31879345›Full record

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

CCR2 inhibition reduces tumor myeloid cells and unmasks a checkpoint inhibitor effect to slow progression of resistant murine gliomas.

Joseph A Flores-Toro, Defang Luo, Adithya Gopinath, Matthew R Sarkisian, James J Campbell, Israel F Charo, Rajinder Singh, Thomas J Schall, Meenal Datta, Rakesh K Jain and 2 more

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 242 papers.

0numbers the graph read from it
0cells of the map it votes in
242citing papers in PubMed
12.9field-weighted citation impact, top 1% 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

242 citing papers in PubMed, 326 citations in OpenAlex.

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182 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

12 authors at 3 institutions in 1 country.

Joseph A Flores-ToroDepartment of Pharmacology & Therapeutics, College of Medicine, University of Florida, Gainesville, FL 32610.
Defang LuoDepartment of Pharmacology & Therapeutics, College of Medicine, University of Florida, Gainesville, FL 32610.
Adithya GopinathDepartment of Pharmacology & Therapeutics, College of Medicine, University of Florida, Gainesville, FL 32610.
Matthew R SarkisianDepartment of Neuroscience, College of Medicine, University of Florida, Gainesville, FL 32610.
James J CampbellChemoCentryx, Mountain View, CA 94043.
Israel F CharoChemoCentryx, Mountain View, CA 94043.
Rajinder SinghChemoCentryx, Mountain View, CA 94043.
Thomas J SchallChemoCentryx, Mountain View, CA 94043.
Meenal DattaEdwin L. Steele Laboratories, Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
Rakesh K JainEdwin L. Steele Laboratories, Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114; jain@steele.mgh.harvard.edu jharriso@ufl.edu.ORCID 0000-0001-7571-3548
Duane A MitchellDepartment of Neurosurgery, College of Medicine, University of Florida, Gainesville, FL 32610.
Jeffrey K HarrisonDepartment of Pharmacology & Therapeutics, College of Medicine, University of Florida, Gainesville, FL 32610; jain@steele.mgh.harvard.edu jharriso@ufl.edu.
University of Florida · USChemoCentryx (United States) · USHarvard University · US

Funding

Using social networks to map and evaluate team science across CTSA hubsUL1TR001427 · NCATS · UNIVERSITY OF FLORIDA · PI MITCHELL, DUANE A. · 2015 to 2024
$37.2M
Dissecting Pediatric Brain Tumor Microenvironment to Improve TreatmentR35CA197743 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI JAIN, RAKESH K. · 2015 to 2020
$5.7M
Reengineering obesity-induced abnormal microenvironment to improve PDAC treatmentR01CA208205 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI FUKUMURA, DAI, JAIN, RAKESH K. · 2017 to 2020
$2.2M
Targeting CCR2-expressing myeloid cells to overcome immune checkpoint inhibitor resistance in gliomaR01NS108781 · NINDS · UNIVERSITY OF FLORIDA · PI HARRISON, JEFFREY K., MITCHELL, DUANE A. · 2018 to 2022
$1.9M
NCATS NIH HHS UL1 TR001427NCI NIH HHS R01 CA208205NCI NIH HHS R35 CA197743NINDS NIH HHS R01 NS108781
6 · The paper itself

Abstract

Immunotherapy directed at the PD-L1/PD-1 axis has produced treatment advances in various human cancers. Unfortunately, progress has not extended to glioblastoma (GBM), with phase III clinical trials assessing anti-PD-1 monotherapy failing to show efficacy in newly diagnosed and recurrent tumors. Myeloid-derived suppressor cells (MDSCs), a subset of immunosuppressive myeloid derived cells, are known to infiltrate the tumor microenvironment of GBM. Growing evidence suggests the CCL2-CCR2 axis is important for this process. This study evaluated the combination of PD-1 blockade and CCR2 inhibition in anti-PD-1-resistant gliomas. CCR2 deficiency unmasked an anti-PD-1 survival benefit in KR158 glioma-bearing mice. CD11b

Indexed as

AnimalsB7-H1 AntigenCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChemokine CCL2CX3C Chemokine Receptor 1Disease Models, AnimalGene Knock-In TechniquesGlioblastomaGliomaHumansImmunotherapyLymphocytes, Tumor-InfiltratingMiceMice, Inbred C57BLMice, KnockoutB7-H1 AntigenCcl2 protein, mouseCcr2 protein, mouseCd274 protein, mouseChemokine CCL2CX3C Chemokine Receptor 1Cx3cr1 protein, mousePdcd1 protein, mouseProgrammed Cell Death 1 ReceptorReceptors, CCR2glioblastomaimmunotherapymyeloid-derived suppressor cellsprogrammed death-1tumor microenvironment

Identifiers

PMID31879345
PMCPMC6969504
OpenAlexW2997058272

What Socratic 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 Socratic graph.