Evidence map›Paper›PMID 33509790›Full record

ArticleCancer immunology research2021

Antitumor T-cell Immunity Contributes to Pancreatic Cancer Immune Resistance.

Reham Ajina, Zoe X Malchiodi, Allison A Fitzgerald, Annie Zuo, Shangzi Wang, Maha Moussa, Connor J Cooper, Yue Shen, Quentin R Johnson, Jerry M Parks and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  6. Review
  7. Multiomics Empowers Predictive Pancreatic Cancer Immunotherapy.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
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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

15 authors at 4 institutions in 1 country.

Reham AjinaDepartment of Oncology and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia.
Zoe X MalchiodiDepartment of Oncology and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia.ORCID 0000-0003-0304-9726
Allison A FitzgeraldDepartment of Oncology and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia.ORCID 0000-0002-2814-0481
Annie ZuoDepartment of Oncology and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia.
Shangzi WangDepartment of Oncology and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia.
Maha MoussaDepartment of Microbiology and Immunology, Georgetown University Medical Center, Washington, District of Columbia.
Connor J CooperGraduate School of Genome Science and Technology, University of Tennessee, Knoxville, Tennessee.ORCID 0000-0002-5527-9948
Yue ShenGraduate School of Genome Science and Technology, University of Tennessee, Knoxville, Tennessee.
Quentin R JohnsonDepartment of Chemistry and Biochemistry, Berry College, Mount Berry, Georgia.ORCID 0000-0002-2860-2877
Jerry M ParksGraduate School of Genome Science and Technology, University of Tennessee, Knoxville, Tennessee.ORCID 0000-0002-3103-9333
Jeremy C SmithDepartment of Chemistry and Biochemistry, Berry College, Mount Berry, Georgia.
Marta CatalfamoDepartment of Microbiology and Immunology, Georgetown University Medical Center, Washington, District of Columbia.
Elana J FertigDepartment of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Sandra A JablonskiDepartment of Oncology and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia.ORCID 0000-0001-7220-8159
Louis M WeinerDepartment of Oncology and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia. weinerl@georgetown.edu.ORCID 0000-0001-5192-0710
Georgetown University · USBerry College · USUniversity of Tennessee at Knoxville · USJohns Hopkins University · US

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI STEPHEN W BYERS · 1990 to 2026
$71.5M
Tumor Antigens for Individual Signatures and TherapyP50CA062924 · NCI · JOHNS HOPKINS UNIVERSITY · PI LENNON, ANNE MARIE · 1993 to 2022
$54.6M
Program for Excellence & Equitty in Research (PEER)R25GM086761 · NIGMS · UNIVERSITY OF TENNESSEE KNOXVILLE · PI ALEXANDRE, GLADYS · 2009 to 2017
$8.6M
TARGETED IMMUNOTHERAPY USING BISPECIFIC ANTIBODIESR01CA050633 · NCI · GEORGETOWN UNIVERSITY · PI WEINER, LOUIS M. · 1989 to 2018
$6.5M
The impact of HIV driven T cell immune activation in angiogenic CD8 T cell function: the role of PAR1 signalingR01AI145549 · NIAID · GEORGETOWN UNIVERSITY · PI CATALFAMO, MARTA L. · 2019 to 2024
$1.9M
Therapeutic/Mechanistic Role of Ape1 in Germ Cell TumorsR01CA094025 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI KELLEY, MARK R. · 2003 to 2007
$1.1M
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001ENCI NIH HHS P30 CA051008NCI NIH HHS P50 CA062924NCI NIH HHS R01 CA050633NCI NIH HHS R01 CA094025NIAID NIH HHS R01 AI145549NIGMS NIH HHS R25 GM086761
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is the third leading cause of cancer death in the United States. Pancreatic tumors are minimally infiltrated by T cells and are largely refractory to immunotherapy. Accordingly, the role of T-cell immunity in pancreatic cancer has been somewhat overlooked. Here, we hypothesized that immune resistance in pancreatic cancer was induced in response to antitumor T-cell immune responses and that understanding how pancreatic tumors respond to immune attack may facilitate the development of more effective therapeutic strategies. We now provide evidence that T-cell-dependent host immune responses induce a PDAC-derived myeloid mimicry phenomenon and stimulate immune resistance. Three KPC mouse models of pancreatic cancer were used: the mT3-2D (Kras

Indexed as

Disease Models, AnimalAnimalsCarcinoma, Pancreatic DuctalCell Line, TumorHumansMetallothionein 3MiceMice, Inbred C57BLMice, SCIDNitrilesPancreasPancreatic NeoplasmsPyrazolesPyrimidinesSignal TransductionT-LymphocytesMetallothionein 3Mt3 protein, mouseNitrilesPyrazolesPyrimidinesRNF123 protein, humanruxolitinibUbiquitin-Protein Ligases

Identifiers

PMID33509790
PMCPMC8283778
OpenAlexW3121869337

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.