Evidence map›Paper›PMID 14713718›Full record

ReviewImmunologic research2003

T-cell anergy: from phenotype to genotype and back.

Christine M Seroogy, C Garrison Fathman

Abstract readReview
PubMed Publisher
In one paragraph

Review in Immunologic research, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

2 authors.

Christine M SeroogyDepartment of Pediatrics, University of Wisconsin, Madison, WI, USA.
C Garrison Fathman

Funding

TERNARY COMPLEX THAT DRIVES T-CELL ACTIVATIONR01CA065237 · NCI · STANFORD UNIVERSITY · PI FATHMAN, CHARLES GARRISON · 1994 to 2013
$3.2M
Novel Anergy Genes as Markers of Immune ToleranceR21AI049903 · NIAID · STANFORD UNIVERSITY · PI FATHMAN, CHARLES GARRISON · 2001 to 2003
$710k
NCI NIH HHS CA65237-14NIAID NIH HHS AI01731-03NIAID NIH HHS AI-49903-02
6 · The paper itself

Abstract

For many decades, anergy has been used as a descriptive term to describe a state of antigen-specific unresponsiveness. A better understanding of this phenotype was revealed in the 1980s using in vitro model systems. These model systems demonstrated that protein synthesis and mobilization of Ca2+ was required leading to the pursuit of a novel gene(s) that would be unique to the anergy phenotype. Several putative "anergy factors" have been suggested. In this review, we provide an overview of the anergy phenotype and proposed anergy-related genes. To date, no single gene has been described that would completely fulfill the criteria of an "anergy factor." We review work from our laboratory describing a novel gene that we have termed Gene Related to Anergy In Lymphocytes (GRAIL) that is upregulated in T cells anergized in vitro and in vivo and, following transduction into T cells, reiterates the anergy phenotype.

Indexed as

Clonal AnergyAnimalsCD4-Positive T-LymphocytesCell CycleGenotypeMicePhenotypeSignal Transduction

Identifiers

PMID14713718

What OpenQuestion holds

Textmetadata
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.