Evidence map›Paper›PMID 32860704›Full record

ArticleThe Journal of experimental medicine2020

Interleukin-17-induced neutrophil extracellular traps mediate resistance to checkpoint blockade in pancreatic cancer.

Yu Zhang, Vidhi Chandra, Erick Riquelme Sanchez, Prasanta Dutta, Pompeyo R Quesada, Amanda Rakoski, Michelle Zoltan, Nivedita Arora, Seyda Baydogan, William Horne and 12 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 302 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
302citing papers in PubMed, 1 pooled it
18.0field-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

302 citing papers in PubMed, 1 synthesis or guideline pooled it, 433 citations in OpenAlex.

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  16. Contextualizing TNature reviews. Immunology · 2026
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242 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

22 authors at 8 institutions in 2 countries.

Yu ZhangDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX.
Vidhi ChandraDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX.
Erick Riquelme SanchezDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX.
Prasanta DuttaCancer Systems Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX.
Pompeyo R QuesadaDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX.
Amanda RakoskiDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX.
Michelle ZoltanDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX.
Nivedita AroraUniversity of Minnesota, Minneapolis, MN.
Seyda BaydoganDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX.
William HorneRichard King Mellon Foundation Institute for Pediatric Research, Children's Hospital of Pittsburgh, Pittsburgh, PA.
Jared BurksDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
Hanwen XuDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX.
Perwez HussainLaboratory of Human Carcinogenesis, National Cancer Institute, Bethesda, MD.
Huamin WangDepartment of Anatomical Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Sonal GuptaDepartment of Anatomical Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Anirban MaitraDepartment of Anatomical Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Jennifer M BaileyDepartment of Gastroenterology, University of Texas Health Sciences Center, Houston, TX.
Seyed J MoghaddamPulmonary Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
Sulagna BanerjeeDepartment of Surgery, Sylvester Comprehensive Cancer Center, University of Miami Health System, Miami, FL.
Ismet SahinDepartment of Engineering, Texas Southern University, Houston, TX.
Pratip BhattacharyaCancer Systems Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX.
Florencia McAllisterDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX.
The University of Texas MD Anderson Cancer Center · USChildren's Hospital of Pittsburgh · USNational Cancer Institute · USTexas Southern University · USThe University of Texas Health Science Center at Houston · USUniversidad Mayor · CLUniversity of Miami Health System · USUniversity of Minnesota · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Paul Calabresi Clinical Oncology AwardK12CA088084 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI David S. Hong, Scott Kopetz · 2000 to 2026
$14.0M
Role of Inflammation in the Development and Progression of Pancreatic CancerZIABC011185 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HUSSAIN, SYED PERWEZ · 2009 to 2023
$10.4M
Dissecting the Source and Mechanisms of IL-17-Mediated Modulation of Pancreatic TumorigenesisR37CA237384 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MCALLISTER, FLORENCIA · 2020 to 2025
$2.6M
Single Cell Spatial Analysis in TissueR50CA243707 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BURKS, JARED KYLE · 2020 to 2024
$1.3M
NCI NIH HHS K12 CA088084NCI NIH HHS P30 CA016672NCI NIH HHS R37 CA237384NCI NIH HHS R50 CA243707
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) remains a lethal malignancy with an immunosuppressive microenvironment that is resistant to most therapies. IL17 is involved in pancreatic tumorigenesis, but its role in invasive PDAC is undetermined. We hypothesized that IL17 triggers and sustains PDAC immunosuppression. We inhibited IL17/IL17RA signaling using pharmacological and genetic strategies alongside mass cytometry and multiplex immunofluorescence techniques. We uncovered that IL17 recruits neutrophils, triggers neutrophil extracellular traps (NETs), and excludes cytotoxic CD8 T cells from tumors. Additionally, IL17 blockade increases immune checkpoint blockade (PD-1, CTLA4) sensitivity. Inhibition of neutrophils or Padi4-dependent NETosis phenocopies IL17 neutralization. NMR spectroscopy revealed changes in tumor lactate as a potential early biomarker for IL17/PD-1 combination efficacy. Higher expression of IL17 and PADI4 in human PDAC corresponds with poorer prognosis, and the serum of patients with PDAC has higher potential for NETosis. Clinical studies with IL17 and checkpoint blockade represent a novel combinatorial therapy with potential efficacy for this lethal disease.

Indexed as

AnimalsBiomarkers, TumorCD8-Positive T-LymphocytesCell Line, TumorDrug Resistance, NeoplasmExtracellular TrapsHumansImmune Checkpoint InhibitorsImmunosuppression TherapyInterleukin-17Lymphocyte ActivationMice, Inbred C57BLNeutrophilsPancreatic NeoplasmsProgrammed Cell Death 1 ReceptorSignal TransductionBiomarkers, TumorImmune Checkpoint InhibitorsInterleukin-17Pdcd1 protein, mouseProgrammed Cell Death 1 Receptor

Identifiers

PMID32860704
PMCPMC7953739
OpenAlexW3082256626

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.