Evidence map›Paper›PMID 22075702›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

Th-1 lymphocytes induce dendritic cell tumor killing activity by an IFN-γ-dependent mechanism.

Collin J LaCasse, Nona Janikashvili, Claire B Larmonier, Darya Alizadeh, Neale Hanke, Jessica Kartchner, Elaine Situ, Sara Centuori, Michael Har-Noy, Bernard Bonnotte and 2 more

5 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 5 registered trials, which are not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
0.9field-weighted citation impact, top 27% 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.

NCT01923233 phase1 / phase2withdrawnnot on this mapstarted 2014, after this paper: background citation

Phase I Feasibility Study of ALLOSTIM(TM) in Combination With Radiofrequency Ablation in Patients With Refractory Hepatocellular Carcinoma

TypeinterventionalSponsorMirror Biologics, Inc.Ran2014 to 2015Enrolled0ConditionsHepatocellular CarcinomaArmsAlloStim
NCT01995227 phase1 / phase2withdrawnnot on this mapstarted 2013, after this paper: background citation

An Individualized Anti-Cancer Vaccine (AlloVaxTM) Study in Patients With Refractory Hepatocellular Carcinoma (HCC)

TypeinterventionalSponsorMirror Biologics, Inc.Ran2013 to 2018Enrolled0ConditionsHepatocellular CarcinomaArmsAlloVax, CRCL, AlloStim
NCT01998542 phase2completednot on this mapstarted 2016, after this paper: background citation

Phase II Study Designed To Evaluate Safety and Tumor Debulking Mechanism of an Individualized Cancer Vaccine (AllovaxTM) in Patients With Metastatic or Recurrent Cancer of the Head and Neck.

TypeinterventionalSponsorMirror Biologics, Inc.Ran2016 to 2017Enrolled12ConditionsCancer of Head and Neck, Squamous Cell Carcinoma of the Head and NeckArmsAlloVax, CRCL, AlloStim
NCT02018419 phase1 / phase2withdrawnnot on this mapstarted 2014, after this paper: background citation

In-Situ Cancer Vaccine: Phase I/IIb, Open-Label Study to Assess Safety of AllostimTM in Combination With Cryoablation in Metastatic Breast Cancer Previously Treated With an Anthracycline, a Taxane and Capecitabine

TypeinterventionalSponsorMirror Biologics, Inc.Ran2014 to 2014Enrolled0ConditionsMetastatic Breast CancerArmsAlloStim, Cryoablation
NCT02380443 phase2completednot on this mapstarted 2016, after this paper: background citation

In-Situ Cancer Vaccine: Phase IIA, Open-Label Study to Assess the Safety of AlloStim® Immunotherapy Alone and in Combination With Cryoablation as Third Line Therapy for Metastatic Colorectal Cancer

TypeinterventionalSponsorMirror Biologics, Inc.Ran2016 to 2018Enrolled13ConditionsColorectal Cancer MetastaticArmsAlloStim, Cryoablation
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  9. TGF-β broadly modifies rather than specifically suppresses reactivated memory CD8 T cells in a dose-dependent manner.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. CD4Nature · 2023
    Article
  11. Article
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  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
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  19. Review
  20. Review
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

12 authors at 3 institutions in 3 countries.

Collin J LaCasseDepartment of Pediatrics, University of Arizona, Tucson, AZ 85724-5073, USA.
Nona Janikashvili
Claire B Larmonier
Darya Alizadeh
Neale Hanke
Jessica Kartchner
Elaine Situ
Sara Centuori
Michael Har-Noy
Bernard Bonnotte
Emmanuel Katsanis
Nicolas Larmonier
University of Arizona · USImmunovative Therapies (Israel) · ILInserm · FR

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
Integrative Cancer Scholars Training GrantT32CA009213 · NCI · UNIVERSITY OF ARIZONA · PI CAREW, JENNIFER S, CURIEL-LEWANDROWSKI, CLARA · 1985 to 2024
$8.6M
Immunotherapy for Chronic Myelogenous LeukemiaR01CA104926 · NCI · UNIVERSITY OF ARIZONA · PI KATSANIS, EMMANUEL · 2004 to 2013
$2.4M
NCI NIH HHS CA023074NCI NIH HHS P30 CA023074NCI NIH HHS R01 CA104926NCI NIH HHS T32 CA009213NCI NIH HHS T32CA009213
6 · The paper itself

Abstract

Dendritic cells (DCs) encompass a heterogeneous population of cells capable of orchestrating innate and adaptive immune responses. The ability of DCs to act as professional APCs has been the foundation for the development and use of these cells as vaccines in cancer immunotherapy. DCs are also endowed with the nonconventional property of directly killing tumor cells. The current study investigates the regulation of murine DC cytotoxic function by T lymphocytes. We provide evidence that CD4(+) Th-1, but not Th-2, Th-17 cells, or regulatory T cells, are capable of inducing DC cytotoxic function. IFN-γ was identified as the major factor responsible for Th-1-induced DC tumoricidal activity. Tumor cell killing mediated by Th-1-activated killer DCs was dependent on inducible NO synthase expression and NO production. Importantly, Th-1-activated killer DCs were capable of presenting the acquired Ags from the killed tumor cells to T lymphocytes in vitro or in vivo. These observations offer new possibilities for the application of killer DCs in cancer immunotherapy.

Indexed as

Cytotoxicity, ImmunologicAnimalsAntigen PresentationBone Marrow CellsCell Line, TumorCoculture TechniquesDendritic CellsFemaleInterferon-gammaInterferon gamma ReceptorMammary Neoplasms, ExperimentalMelanoma, ExperimentalMiceMice, 129 StrainMice, Inbred BALB CMice, Inbred C57BLInterferon-gammaInterferon gamma ReceptorReceptors, Interferon

Identifiers

PMID22075702
PMCPMC3297475
OpenAlexW2098979383

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.