Evidence map›Paper›PMID 30730851›Full record

ArticleJCI insight2019

Mature neutrophils suppress T cell immunity in ovarian cancer microenvironment.

Kelly L Singel, Tiffany R Emmons, Anm Nazmul H Khan, Paul C Mayor, Shichen Shen, Jerry T Wong, Kayla Morrell, Kevin H Eng, Jaron Mark, Richard B Bankert and 11 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
6.9field-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

99 citing papers in PubMed, 129 citations in OpenAlex.

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39 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

21 authors at 5 institutions in 2 countries.

Kelly L SingelDepartment of Immunology.
Tiffany R EmmonsDepartment of Immunology.
Anm Nazmul H KhanDepartment of Internal Medicine, and.
Paul C MayorDepartment of Surgery, Division of Gynecologic Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Shichen ShenNew York State Center of Excellence Bioinformatics and Life Sciences, University at Buffalo, Buffalo, New York, USA.
Jerry T WongDepartment of Pathology and Laboratory Medicine and.
Kayla MorrellDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Kevin H EngDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Jaron MarkDepartment of Surgery, Division of Gynecologic Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Richard B BankertDepartment of Microbiology and Immunology, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York, USA.
Junko MatsuzakiCenter for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Richard C KoyaCenter for Immunotherapy, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Anna M BlomDivision of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, Sweden.
Kenneth R McLeishDepartment of Medicine, University of Louisville School of Medicine, Louisville, Kentucky, USA.
Jun QuNew York State Center of Excellence Bioinformatics and Life Sciences, University at Buffalo, Buffalo, New York, USA.
Sanjay RamDepartment of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Kirsten B MoysichDepartment of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Scott I AbramsDepartment of Immunology.
Kunle OdunsiDepartment of Surgery, Division of Gynecologic Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Emese ZsirosDepartment of Surgery, Division of Gynecologic Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Brahm H SegalDepartment of Immunology.
Roswell Park Comprehensive Cancer Center · USUniversity at Buffalo, State University of New York · USLund University · SEUniversity of Louisville · USUniversity of Massachusetts Chan Medical School · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
RPCI-UPCI Ovarian Cancer SPOREP50CA159981 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MOYSICH, KIRSTEN B. · 2013 to 2025
$19.6M
Novel immunological biomarkers ovarian cancer prognosisR01CA188900 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MOYSICH, KIRSTEN B., SEGAL, BRAHM H. · 2015 to 2019
$3.3M
MULTIDISCIPLINARY APPROACHES TUMOR IMMUNOLOGYT32CA085183 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Scott I. Abrams · 2001 to 2026
$3.1M
Postdoctoral Research Training in Surgical OncologyT32CA108456 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI YENDAMURI, SAIKRISHNA · 2006 to 2020
$2.8M
Mechanisms Underlying Functional Programs of Tumor-Associated MacrophagesR01CA172105 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI ABRAMS, SCOTT I. · 2015 to 2019
$2.0M
TGFbeta Blockade in MART TCR-Engineered T Cell Melanoma Immunotherapy in ManR01CA164333 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KOYA, RICHARD C · 2013 to 2017
$1.4M
Informatic Methods for Differential Signaling and Immune Co-Regulatory ExpressionK01LM012100 · NLM · ROSWELL PARK CANCER INSTITUTE CORP · PI ENG, KEVIN HASEGAWA · 2015 to 2017
$502k
NCI NIH HHS P30 CA016056NCI NIH HHS P50 CA159981NCI NIH HHS R01 CA164333NCI NIH HHS R01 CA172105NCI NIH HHS R01 CA188900NCI NIH HHS T32 CA085183NCI NIH HHS T32 CA108456NLM NIH HHS K01 LM012100
6 · The paper itself

Abstract

Epithelial ovarian cancer (EOC) often presents with metastases and ascites. Granulocytic myeloid-derived suppressor cells are an immature population that impairs antitumor immunity. Since suppressive granulocytes in the ascites of patients with newly diagnosed EOC were morphologically mature, we hypothesized that PMN were rendered suppressive in the tumor microenvironment (TME). Circulating PMN from patients were not suppressive but acquired a suppressor phenotype (defined as ≥1 log10 reduction of anti-CD3/CD28-stimulated T cell proliferation) after ascites supernatant exposure. Ascites supernatants (20 of 31 supernatants) recapitulated the suppressor phenotype in PMN from healthy donors. T cell proliferation was restored with ascites removal and restimulation. PMN suppressors also inhibited T cell activation and cytokine production. PMN suppressors completely suppressed proliferation in naive, central memory, and effector memory T cells and in engineered tumor antigen-specific cytotoxic T lymphocytes, while antigen-specific cell lysis was unaffected. Inhibition of complement C3 activation and PMN effector functions, including CR3 signaling, protein synthesis, and vesicular trafficking, abrogated the PMN suppressor phenotype. Moreover, malignant effusions from patients with various metastatic cancers also induced the C3-dependent PMN suppressor phenotype. These results point to PMN impairing T cell expansion and activation in the TME and the potential for complement inhibition to abrogate this barrier to antitumor immunity.

Indexed as

ImmunityAgedCD28 AntigensCell ProliferationComplement C3CytokinesFemaleGranulocytesHumansLymphocyte ActivationMuromonab-CD3Myeloid-Derived Suppressor CellsNeutrophilsOvarian NeoplasmsT-LymphocytesTumor MicroenvironmentCD28 AntigensComplement C3CytokinesMuromonab-CD3ComplementImmunologyNeutrophilsOncologyT cells

Identifiers

PMID30730851
PMCPMC6483507
OpenAlexW2913394608

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.