Evidence map›Paper›PMID 36706760›Full record

ArticleCancer cell2023

Neutrophil-activating therapy for the treatment of cancer.

Ian L Linde, Tyler R Prestwood, Jingtao Qiu, Genay Pilarowski, Miles H Linde, Xiangyue Zhang, Lei Shen, Nathan E Reticker-Flynn, David Kung-Chun Chiu, Lauren Y Sheu and 4 more

Open access · greenAbstract read
In one paragraph

Article in Cancer cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed
30.2field-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

125 citing papers in PubMed, 184 citations in OpenAlex.

  1. Trial
  2. Article
  3. CAR-engineered neutrophils derived from induced pluripotent stem cells: a new frontier in cellular immunotherapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  4. Leveraging Microphysiological Systems to Facilitate Neutrophil-Based Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  5. Neutrophils in cancer.Nature reviews. Cancer · 2026
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Albumin-Bound STING Agonist Reprograms HSPCs to Antitumor Neutrophils Enhancing CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  18. Article
  19. Article
  20. Psoriasis-like disease prevents squamous skin tumor development by neutrophil-driven inflammation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article

65 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Ian L LindeProgram in Immunology, Stanford University, Stanford, CA 94305, USA; Department of Pathology, Stanford University, Stanford, CA 94305, USA.
Tyler R PrestwoodDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Jingtao QiuDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Genay PilarowskiDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Miles H LindeProgram in Immunology, Stanford University, Stanford, CA 94305, USA.
Xiangyue ZhangDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Lei ShenDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Nathan E Reticker-FlynnDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
David Kung-Chun ChiuDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Lauren Y SheuDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Simon Van DeursenDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Lorna L TolentinoDepartment of Pathology, Stanford University, Stanford, CA 94305, USA.
Wen-Chao SongDepartment of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Edgar G EnglemanProgram in Immunology, Stanford University, Stanford, CA 94305, USA; Department of Pathology, Stanford University, Stanford, CA 94305, USA. Electronic address: edengleman@stanford.edu.
Stanford University · USTranslational Therapeutics (United States) · US

Funding

Spatial-Genomic Integrative Multi-Species Analysis of Lymph Node MetastasisU54CA209971 · NCI · STANFORD UNIVERSITY · PI NOLAN, GARRY P, PLEVRITIS, SYLVIA KATINA · 2016 to 2021
$11.0M
Project 3: Impact of tumor genetics on PDAC immunobiology and responses to macrophage-targeted immunotherapyP01CA244114 · NCI · STANFORD UNIVERSITY · PI KIM, SEUNG K · 2021 to 2025
$10.0M
Pathogenesis and therapy of dense deposit disease in a mouse modelR01AI085596 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI SONG, WENCHAO · 2010 to 2019
$3.5M
Targeting Lymph Node Dependent Immune Tolerance in CancerR01CA251174 · NCI · STANFORD UNIVERSITY · PI EDGAR G. ENGLEMAN · 2021 to 2026
$3.2M
Innate Immune Mechanisms Contributing to Cancer Growth in ObesityR01CA262361 · NCI · STANFORD UNIVERSITY · PI ENGLEMAN, EDGAR G. · 2021 to 2025
$2.9M
MASPs as therapeutic targets in complement-mediated diseasesR01AI146162 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI SONG, WENCHAO · 2020 to 2024
$2.9M
Effects of FLASH Radiation on Cancer and the Immune ResponseR01CA233958 · NCI · STANFORD UNIVERSITY · PI ENGLEMAN, EDGAR G., LOO, BILLY W · 2019 to 2024
$2.7M
Program in Translational and Experimental HematologyT32HL120824 · NHLBI · STANFORD UNIVERSITY · PI MAJETI, RAVINDRA · 2014 to 2023
$2.4M
Targeting Dectin-2 on Tumor-associated Macrophages for the Treatment of CancerR01CA222969 · NCI · STANFORD UNIVERSITY · PI ENGLEMAN, EDGAR G. · 2018 to 2022
$2.1M
Complement dysregulation and atypical hemolytic uremic syndromeR01AI117410 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI SONG, WENCHAO · 2015 to 2019
$2.0M
Development of a glycopeptide vaccine for cancer metastasisF32CA189408 · NCI · STANFORD UNIVERSITY · PI RETICKER-FLYNN, NATHAN EDWARD · 2014 to 2016
$164k
Mechanistic basis of allogeneic IgG-induced tumor eradicationF31CA196029 · NCI · STANFORD UNIVERSITY · PI LINDE, IAN LISLE · 2015 to 2017
$127k
NCI NIH HHS F30 CA196145NCI NIH HHS F31 CA196029NCI NIH HHS F32 CA189408NCI NIH HHS P01 CA244114NCI NIH HHS R01 CA222969NCI NIH HHS R01 CA233958NCI NIH HHS R01 CA251174NCI NIH HHS R01 CA262361NCI NIH HHS U54 CA209971NHLBI NIH HHS T32 HL120824NIAID NIH HHS R01 AI085596NIAID NIH HHS R01 AI117410NIAID NIH HHS R01 AI146162
6 · The paper itself

Abstract

Despite their cytotoxic capacity, neutrophils are often co-opted by cancers to promote immunosuppression, tumor growth, and metastasis. Consequently, these cells have received little attention as potential cancer immunotherapeutic agents. Here, we demonstrate in mouse models that neutrophils can be harnessed to induce eradication of tumors and reduce metastatic seeding through the combined actions of tumor necrosis factor, CD40 agonist, and tumor-binding antibody. The same combination activates human neutrophils in vitro, enabling their lysis of human tumor cells. Mechanistically, this therapy induces rapid mobilization and tumor infiltration of neutrophils along with complement activation in tumors. Complement component C5a activates neutrophils to produce leukotriene B

Indexed as

Antineoplastic AgentsNeoplasmsAnimalsHumansLeukotriene B4MiceNeutrophilsTumor Necrosis Factor-alphaAntineoplastic AgentsLeukotriene B4Tumor Necrosis Factor-alphaC5acancer immunotherapyCD40complementleukotriene B4neutrophilreactive oxygen speciestumor immunologytumor necrosis factorxanthine oxidase

Identifiers

PMID36706760
PMCPMC9968410
OpenAlexW4318070682

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.