Evidence map›Paper›PMID 19342643›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Tumor recognition and self-recognition induce distinct transcriptional profiles in antigen-specific CD4 T cells.

Derese Getnet, Charles H Maris, Edward L Hipkiss, Joseph F Grosso, Timothy J Harris, Hung-Rong Yen, Tullia C Bruno, Satoshi Wada, Adam Adler, Robert W Georgantas and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Rat and fish peripheral blood leukocytes respond distinctively toFrontiers in cellular and infection microbiology · 2022
    Article
  2. Review
  3. Targeting the spectrum of immune checkpoints in prostate cancer.Expert review of clinical pharmacology · 2021
    Review
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  17. Immunotherapy for prostate cancer: biology and therapeutic approaches.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2011
    Review
  18. Article
  19. Article
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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

14 authors at 4 institutions in 2 countries.

Derese GetnetDepartment of Oncology, Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD 21231, USA.
Charles H Maris
Edward L Hipkiss
Joseph F Grosso
Timothy J Harris
Hung-Rong Yen
Tullia C Bruno
Satoshi Wada
Adam Adler
Robert W Georgantas
Chunfa Jie
Monica V Goldberg
Drew M Pardoll
Charles G Drake
Sidney Kimmel Comprehensive Cancer Center · USChang Gung Memorial Hospital · TWJohns Hopkins University · USUConn Health · US

Funding

Analysis of Lag-3 in Regulatory T Cell Function and Immune SupressionR01CA127153 · NCI · JOHNS HOPKINS UNIVERSITY · PI DRAKE, CHARLES G. · 2008 to 2012
$1.7M
Regulation of the Immune Response to Prostate CancerK08CA096948 · NCI · JOHNS HOPKINS UNIVERSITY · PI DRAKE, CHARLES G · 2003 to 2007
$684k
NCI NIH HHS K08 CA096948NCI NIH HHS R01 CA127153
6 · The paper itself

Abstract

Tumors express a wide variety of both mutated and nonmutated Ags. Whether these tumor Ags are broadly recognized as self or foreign by the immune system is currently unclear. Using an autochthonous prostate cancer model in which hemagglutinin (HA) is specifically expressed in the tumor (ProHA x TRAMP mice), as well as an analogous model wherein HA is expressed in normal tissues as a model self-Ag (C3HA(high)), we examined the transcriptional profile of CD4 T cells undergoing Ag-specific division. Consistent with our previous data, transfer of Ag-specific CD4 T cells into C3HA(high) resulted in a functionally inactivated CD4 T cell profile. Conversely, adoptive transfer of an identical CD4 T cell population into ProHA x TRAMP mice resulted in the induction of a regulatory phenotype of the T cell (Treg) both at the transcriptional and functional level. Interestingly, this Treg skewing was a property of even early-stage tumors, suggesting Treg induction as an important tolerance mechanism during tumor development.

Indexed as

AnimalsAntigensCD4-Positive T-LymphocytesCell ProliferationDown-RegulationForkhead Transcription FactorsGene Expression ProfilingMiceNeoplasmsPhenotypeRatsTranscription, GeneticUp-RegulationAntigensForkhead Transcription FactorsFoxp3 protein, mouse

Identifiers

PMID19342643
PMCPMC3082355
OpenAlexW2112331258

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.