Evidence map›Paper›PMID 20488579›Full record

ArticleImmunobiology

Peritoneal T lymphocyte regulation by macrophages.

G Composto, D Gonzalez, A Bucknum, D Silberman, J Taylor, M Kozlowski, T Bloomfield, T Bartlett, J Riggs

Abstract read
In one paragraph

Article in Immunobiology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

G CompostoDepartment of Biology, Rider University, Lawrenceville, NJ 08648-3099, USA.
D Gonzalez
A Bucknum
D Silberman
J Taylor
M Kozlowski
T Bloomfield
T Bartlett
J Riggs
Rider University · US

Funding

Macrophage Density Regulates T CellsR15CA136901 · NCI · RIDER UNIVERSITY · PI RIGGS, JAMES EDWARD · 2009 to 2009
$199k
Immunosenescence in TCR-Transgenic Bone Marrow ChimerasR15AG019631 · NIA · RIDER UNIVERSITY · PI RIGGS, JAMES E · 2001 to 2001
$133k
RECONSTRUCTION OF SUPERANTIGEN TOLERANT IMMUNITYR15AI037975 · NIAID · RIDER UNIVERSITY · PI RIGGS, JAMES E · 1995 to 1995
–
AGING, IMMUNODEFICIENCY, AND S AGS IN B LYMPHOMAGENESISR15CA077814 · NCI · RIDER UNIVERSITY · PI RIGGS, JAMES E · 1998 to 1999
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T CELL TOLERANCE INDUCED BY B CELLS IN THE NEONATER15HD029206 · NICHD · RIDER UNIVERSITY · PI RIGGS, JAMES E · 1992 to 1992
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NCI NIH HHS CA77814-01NCI NIH HHS R15 CA136901NIAID NIH HHS AI37975-01NIA NIH HHS AG19631-01NIA NIH HHS R15 AG019631NICHD NIH HHS R15 HD29206-01
6 · The paper itself

Abstract

The T cell composition of the peritoneal cavity (PerC) in naïve BALB/c, C57BL/6, DBA/2J, and B-1 B cell-defective BALB.xid mice was investigated. The BALB.xid PerC T cell pool had a high CD4:CD8 T cell ratio relative to the other strains whose ratios were similar to those found in their lymph node and spleen. All mice had significant representation of T cells with an activated (CD25(+), GITR(hi), CD44(hi), CD45RB(lo), CD62L(lo)) phenotype and low numbers of Foxp3(+) T(reg) cells in their PerC. Despite a phenotype indicative of activation, peritoneal T cell responses to CD3 ligation were very low for C57BL/6 and BALB.xid, but not BALB/c, mice. Enzyme inhibition and cytokine neutralization studies revealed active suppression of the T cell response mediated by the macrophages that represent a significant portion of PerC leucocytes. Driven by IFNγ to express iNOS, macrophages suppressed T cell activation in vitro by arginine catabolism. Although BALB/c T cells were also in a macrophage-dense environment their limited IFNγ production failed to trigger suppression. This difference between BALB/c and BALB.xid PerC T cells suggests a role for xid in shaping macrophage-mediated immune regulation.

Indexed as

Immune ToleranceAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell CommunicationCells, CulturedForkhead Transcription FactorsGlucocorticoid-Induced TNFR-Related ProteinImmunologic MemoryInterleukin-2 Receptor alpha SubunitMacrophages, PeritonealMiceMice, Inbred StrainsMice, Mutant StrainsReceptors, Nerve Growth FactorReceptors, Tumor Necrosis FactorForkhead Transcription FactorsFoxp3 protein, mouseGlucocorticoid-Induced TNFR-Related ProteinInterleukin-2 Receptor alpha SubunitReceptors, Nerve Growth FactorReceptors, Tumor Necrosis FactorTnfrsf18 protein, mouse

Identifiers

PMID20488579
PMCPMC2935942
OpenAlexW1965346503

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.