Evidence map›Paper›PMID 31848188›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

Inhibition of MDSC Trafficking with SX-682, a CXCR1/2 Inhibitor, Enhances NK-Cell Immunotherapy in Head and Neck Cancer Models.

Sarah Greene, Yvette Robbins, Wojciech K Mydlarz, Angel P Huynh, Nicole C Schmitt, Jay Friedman, Lucas A Horn, Claudia Palena, Jeffrey Schlom, Dean Y Maeda and 3 more

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 204 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
204citing papers in PubMed, 1 pooled it
8.7field-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

204 citing papers in PubMed, 1 synthesis or guideline pooled it, 266 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Leveraging Microphysiological Systems to Facilitate Neutrophil-Based Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  6. Article
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  9. Emerging Immune-Based Therapeutic Strategies in Hepatocellular Carcinoma.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
  10. Review
  11. Interleukin-8 in health and disease.Molecular biomedicine · 2026
    Review
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  14. Article
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144 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

13 authors at 5 institutions in 1 country.

Sarah GreeneTranslational Tumor Immunology Program, National Institute on Deafness and Other Communication Disorders, Bethesda, Maryland.ORCID 0000-0001-5223-3525
Yvette RobbinsTranslational Tumor Immunology Program, National Institute on Deafness and Other Communication Disorders, Bethesda, Maryland.
Wojciech K MydlarzDepartment of Otolaryngology-Head and Neck Surgery, Johns Hopkins School of Medicine, Baltimore, Maryland.
Angel P HuynhTranslational Tumor Immunology Program, National Institute on Deafness and Other Communication Disorders, Bethesda, Maryland.
Nicole C SchmittDepartment of Otolaryngology-Head and Neck Surgery, Johns Hopkins School of Medicine, Baltimore, Maryland.
Jay FriedmanTranslational Tumor Immunology Program, National Institute on Deafness and Other Communication Disorders, Bethesda, Maryland.
Lucas A HornLaboratory of Tumor Immunology and Biology, NCI, Bethesda, Maryland.
Claudia PalenaLaboratory of Tumor Immunology and Biology, NCI, Bethesda, Maryland.
Jeffrey SchlomLaboratory of Tumor Immunology and Biology, NCI, Bethesda, Maryland.ORCID 0000-0001-7932-4072
Dean Y MaedaSyntrix Pharmaceuticals, Auburn, Washington.ORCID 0000-0002-9304-6846
John A ZebalaSyntrix Pharmaceuticals, Auburn, Washington.ORCID 0000-0002-3581-6750
Paul E ClavijoTranslational Tumor Immunology Program, National Institute on Deafness and Other Communication Disorders, Bethesda, Maryland.
Clint AllenTranslational Tumor Immunology Program, National Institute on Deafness and Other Communication Disorders, Bethesda, Maryland. clint.allen@nih.gov.
National Institute on Deafness and Other Communication Disorders · USCenter for Cancer Research · USJohns Hopkins University · USSyntrix Biosystems (United States) · USFoundation for the National Institutes of Health · US

Funding

Characterization and Enhancement of Anti-Tumor Immune Responses in Head and Neck CancerZIADC000087 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI ALLEN, CLINT · 2015 to 2022
$13.5M
Novel Targets for Vaccine TherapyZICBC010937 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PALENA, CLAUDIA · 2010 to 2022
$13.2M
Mechanisms and Optimal Combinations of Cisplatin Chemotherapy for Head and Neck Squamous Cell CarcinomaZIADC000090 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI SCHMITT, NICOLE · 2016 to 2020
$3.9M
Intramural NIH HHS ZIA DC000087
6 · The paper itself

Abstract

purposeNatural killer (NK)-cell-based immunotherapy may overcome obstacles to effective T-cell-based immunotherapy such as the presence of genomic alterations in IFN response genes and antigen presentation machinery. All immunotherapy approaches may be abrogated by the presence of an immunosuppressive tumor microenvironment present in many solid tumor types, including head and neck squamous cell carcinoma (HNSCC). Here, we studied the role of myeloid-derived suppressor cells (MDSC) in suppressing NK-cell function in HNSCC. EXPERIMENTAL

designThe ability of peripheral and tumor-infiltrating MDSC from mice bearing murine oral cancer 2 (MOC2) non-T-cell-inflamed tumors and from patients with HNSCC to suppress NK-cell function was studied with real-time impedance and ELISpot assays. The therapeutic efficacy of SX-682, a small-molecule inhibitor of CXCR1 and CXCR2, was assessed in combination with adoptively transferred NK cells.

resultsMice bearing MOC2 tumors pathologically accumulate peripheral CXCR2

conclusionsThe clinical study of CXCR1/2 inhibitors in combination with adoptively transferred NK cells is warranted.

Indexed as

AnimalsAntineoplastic Agents, ImmunologicalCell Line, TumorDisease Models, AnimalHead and Neck NeoplasmsHumansImmunotherapyKiller Cells, NaturalLeukocytes, MononuclearMiceMice, Inbred C57BLMouth NeoplasmsMyeloid-Derived Suppressor CellsReceptors, Interleukin-8AReceptors, Interleukin-8BTransforming Growth Factor betaAntineoplastic Agents, ImmunologicalReceptors, Interleukin-8AReceptors, Interleukin-8BTransforming Growth Factor beta

Identifiers

PMID31848188
PMCPMC7073293
OpenAlexW2995367800

What OpenQuestion holds

Textmetadata
LicenceTDM
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.