Evidence map›Paper›PMID 34632444›Full record

ArticleCell reports methods2021

A mouse model for the study of anti-tumor T cell responses in Kras-driven lung adenocarcinoma.

Brittany Fitzgerald, Kelli A Connolly, Can Cui, Eric Fagerberg, Dylan L Mariuzza, Noah I Hornick, Gena G Foster, Ivana William, Julie F Cheung, Nikhil S Joshi

Open access · goldAbstract read
In one paragraph

Article in Cell reports methods, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  8. Article
  9. Review
  10. Article
  11. Article
  12. Leveraging T cells for cancer immunotherapy.Immunity & inflammation · 2025
    Review
  13. Fuel for thought: targeting metabolism in lung cancer.Translational lung cancer research · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

10 authors at 1 institution in 1 country.

Brittany FitzgeraldDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06519, USA.
Kelli A ConnollyDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06519, USA.
Can CuiDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06519, USA.
Eric FagerbergDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06519, USA.
Dylan L MariuzzaDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06519, USA.
Noah I HornickDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06519, USA.
Gena G FosterDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06519, USA.
Ivana WilliamDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06519, USA.
Julie F CheungDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06519, USA.
Nikhil S JoshiDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 06519, USA.
Yale University · US

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI MEGAN C KING · 1985 to 2026
$85.0M
Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI Kevan C Herold, GERALD I SHULMAN · 1993 to 2026
$44.0M
Yale SPORE in Lung Cancer (YSILC): The Biology and Personalized Treatment of Lung CancerP50CA196530 · NCI · YALE UNIVERSITY · PI Kurt A Schalper · 2015 to 2026
$31.1M
Yale Liver CenterP30DK034989 · NIDDK · YALE UNIVERSITY · PI YASUKO IWAKIRI · 1986 to 2026
$31.1M
INTERDISCIPLINARY IMMUNOLOGY TRAINING PROGRAMT32AI007019 · NIAID · YALE UNIVERSITY · PI Carrie L. Lucas, David G. Schatz · 1985 to 2026
$14.4M
IMMUNOHEMATOLOGY/TRANSFUSION MEDICINE RESEARCH TRAININGT32HL007974 · NHLBI · YALE UNIVERSITY · PI JEANNE E HENDRICKSON, Diane S Krause · 2001 to 2026
$8.1M
Training in Investigative DermatologyT32AR007016 · NIAMS · YALE UNIVERSITY · PI KEITH A CHOATE, MICHAEL GIRARDI · 1986 to 2026
$7.8M
Yale Cancer Center Advanced Training Program for Physician-Scientists (YCC-ATPP)T32CA233414 · NCI · YALE UNIVERSITY · PI Eric P. Winer · 2019 to 2026
$3.2M
Developing translationally-relevant genetically engineered mouse models of lung adenocarcinoma for investigations in cancer immunologyR01CA237037 · NCI · YALE UNIVERSITY · PI JOSHI, NIKHIL · 2020 to 2024
$2.7M
Human and Translational Immunology Training ProgramT32AI155387 · NIAID · YALE UNIVERSITY · PI Joseph Edgar Craft, Kevan C Herold · 2021 to 2026
$2.6M
Investigating the development and maintenance of tumor-associated tertiary lymphoid structures in an autochthonous mouse model of lung adenocarcinomaK22CA200912 · NCI · YALE UNIVERSITY · PI JOSHI, NIKHIL · 2016 to 2018
$587k
NCI NIH HHS K22 CA200912NCI NIH HHS P30 CA016359NCI NIH HHS P50 CA196530NCI NIH HHS R01 CA237037NCI NIH HHS T32 CA233414NHLBI NIH HHS T32 HL007974NIAID NIH HHS T32 AI007019NIAID NIH HHS T32 AI155387NIAMS NIH HHS T32 AR007016NIDDK NIH HHS P30 DK034989NIDDK NIH HHS P30 DK045735
6 · The paper itself

Abstract

Kras-driven lung adenocarcinoma (LUAD) is the most common lung cancer. A significant fraction of patients with Kras-driven LUAD respond to immunotherapy, but mechanistic studies of immune responses against LUAD have been limited because of a lack of immunotherapy-responsive models. We report the development of the immunogenic KP × NINJA (inversion inducible joined neoantigen) (KP-NINJA) LUAD model. This model allows temporal uncoupling of antigen and tumor induction, which allows one to wait until after infection-induced inflammation has subsided to induce neoantigen expression by tumors. Neoantigen expression is restricted to EPCAM+ cells in the lung and expression of neoantigen was more consistent between tumors than when neoantigens were encoded on lentiviruses. Moreover, tumors were infiltrated by tumor-specific CD8 T cells. Finally, LUAD cell lines derived from KP-NINJA mice were immunogenic and responded to immune checkpoint therapy (anti-PD1 and anti-CTLA4), providing means for future studies into the immunobiology of therapeutic responses in LUAD.

Indexed as

Adenocarcinoma of LungLung NeoplasmsAnimalsAntibodiesCD8-Positive T-LymphocytesMiceAntibodies

Identifiers

PMID34632444
PMCPMC8500377
OpenAlexW3199242190

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.