Evidence map›Paper›PMID 18308639›Full record

ArticleClinical immunology (Orlando, Fla.)2008

TGFbeta1 deficiency does not affect the generation and maintenance of CD4+CD25+FOXP3+ putative Treg cells, but causes their numerical inadequacy and loss of regulatory function.

Ramireddy Bommireddy, George F Babcock, Ram R Singh, Thomas Doetschman

Open access · greenAbstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

4 authors at 3 institutions in 1 country.

Ramireddy BommireddyBIO5 Institute, University of Arizona, PO Box 245217, Tucson, AZ 85724-5217, USA.
George F Babcock
Ram R Singh
Thomas Doetschman
University of Arizona · USUniversity of California, Los Angeles · USUniversity of Cincinnati Medical Center · US

Funding

REPRODUCTIVE AND DEVELOPMENTAL TOXICOLOGY RESEARCHP30ES006096 · NIEHS · UNIVERSITY OF CINCINNATI · PI YADAV, JAGJIT S · 1992 to 2022
$35.4M
MOUSE MODELS OF GASTROINTESTINAL CANCERU01CA084291 · NCI · UNIVERSITY OF CINCINNATI · PI GRODEN, JOANNA LOUISE · 1999 to 2008
$6.6M
Transforming Growth Factor beta in T-Cell Homeostasis and ToleranceR01AI067903 · NIAID · UNIVERSITY OF CINCINNATI · PI DOETSCHMAN, THOMAS · 2006 to 2010
$1.8M
TARGETED MUTATION OF TGF-BETA-1 IN ES CELLSR01HD026471 · NICHD · UNIVERSITY OF CINCINNATI · PI DOETSCHMAN, THOMAS · 1990 to 2005
$1.8M
Kidney Damage in Murine LupusR01AR050797 · NIAMS · UNIVERSITY OF CINCINNATI · PI SINGH, RAM RAJ · 2003 to 2006
$1.4M
Peptide Gene Vaccination in LupusR01AR047322 · NIAMS · UNIVERSITY OF CINCINNATI · PI SINGH, RAM RAJ · 2001 to 2005
$1.3M
NCCIH NIH HHS AT50797NCI NIH HHS CA84291NCI NIH HHS U01 CA084291NIAID NIH HHS R01 AI067903NIAMS NIH HHS AR47322NIAMS NIH HHS R01 AR047322NIAMS NIH HHS R01 AR050797NICHD NIH HHS HD26471NICHD NIH HHS R01 HD026471NIEHS NIH HHS ES06096NIEHS NIH HHS P30 ES006096
6 · The paper itself

Abstract

TGFbeta1 is considered to be required for peripheral maintenance of CD4(+)CD25(+)FOXP3(+) T(reg) cells. However, we demonstrate no reduction in the percentage of such T cells in the spleens and thymi of Tgfb1(-/-) mice. Although putative T(reg) cells, characterized as CD4(+)CD25(+)FOXP3(+)CD62L(+) T cells, are increased in Tgfb1(-/-) mice, they may be inadequate to control activated T cells since the ratio of activated T cells:putative T(reg) cells is several-fold higher in Tgfb1(-/-) mice than in control mice. We further show that whereas Tgfb1(-/-) mice that express a chicken OVA-specific TCR transgene (DO11.10) have an increase in putative T(reg) cells, there are no detectable CD4(+)CD25(+) T cells in the spleens of DO11.10 Rag1(-/-) mice suggesting that T(reg)-cell generation is self-antigen dependent regardless of whether they express Tgfb1. Finally, we demonstrate that Tgfb1(-/-) T cells remain responsive to the suppressive effect of TGFbeta1 in vitro. These data suggest that TGFbeta1 is required for the regulatory function of T(reg) cells to prevent activation of T cells and autoimmunity.

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, T-LymphocyteAutoimmunityCD69 AntigensCell ProliferationFlow CytometryForkhead Transcription FactorsImmune ToleranceLectins, C-TypeL-SelectinMiceMice, Inbred BALB CMice, KnockoutMice, TransgenicPhenotypeAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensForkhead Transcription FactorsFoxp3 protein, mouseLectins, C-TypeL-SelectinTransforming Growth Factor beta1

Identifiers

PMID18308639
PMCPMC2387055
OpenAlexW2072482112

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.