Evidence map›Paper›PMID 19950175›Full record

ArticleEuropean journal of immunology2010

Adenosine mediated desensitization of cAMP signaling enhances T-cell responses.

Ailian Yang, Ashley D Mucsi, Melanie D Desrosiers, Jiang-Fan Chen, Jürgen B Schnermann, Michael R Blackburn, Yan Shi

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2010. 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
0.9field-weighted citation impact, top 28% 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, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Purinergic signalling and immune cells.Purinergic signalling · 2014
    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

7 authors at 4 institutions in 2 countries.

Ailian YangImmunology Research Group and Department of Microbiology and Infectious Diseases, University of Calgary, Calgary, Alta., Canada.
Ashley D Mucsi
Melanie D Desrosiers
Jiang-Fan Chen
Jürgen B Schnermann
Michael R Blackburn
Yan Shi
University of Calgary · CABoston University · USNational Institute of Diabetes and Digestive and Kidney Diseases · USThe University of Texas Health Science Center at Houston · US

Funding

The biological relevance of adenosine deamination in immune activationR21AI073630 · NIAID · UNIVERSITY OF CALGARY · PI SHI, YAN · 2007 to 2008
$294k
CIHRIntramural NIH HHS Z99 DA999999Intramural NIH HHS Z99 DK999999Intramural NIH HHS Z99 OD999999NIAID NIH HHS R21 AI073630
6 · The paper itself

Abstract

Adenosine has long been regarded as a crucial anti-inflammatory agent that protects the host from excessive damage. It has been reported to play an important role in suppressing immune activation, particularly that of T cells. However, it is a general observation that induction of T-cell activation is an efficient event despite the high adenosine levels that are often present in the affected host due to injury or stress. We report here that prior to antigenic stimulation via TCR/CD3, exposure of T cells to adenosine desensitizes adenosine receptors, so as to create a window of time where the T cells are insensitive to this ubiquitous suppressor. T cells from mice that were pre-exposed to this manipulation showed stronger responses to antigenic stimulation; therefore, the P1 adenosine receptor desensitization demonstrated an adjuvant-like effect. Our results suggest that adenosine receptor desensitization may be a mechanism for T cells to escape the general suppression during early points of T-cell activation and may emerge as a potential alternative for vaccine adjuvants.

Indexed as

AdenosineAdenosine-5'-(N-ethylcarboxamide)Adenosine A1 Receptor AgonistsAdenosine A1 Receptor AntagonistsAdenosine A2 Receptor AgonistsAdenosine A2 Receptor AntagonistsAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCells, CulturedCyclic AMPLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutMice, Transgenic1,3-dipropyl-8-cyclopentylxanthineAdenosineAdenosine-5'-(N-ethylcarboxamide)Adenosine A1 Receptor AgonistsAdenosine A1 Receptor AntagonistsAdenosine A2 Receptor AgonistsAdenosine A2 Receptor AntagonistsCyclic AMPReceptor, Adenosine A1Receptor, Adenosine A2AXanthines

Identifiers

PMID19950175
PMCPMC3468332
OpenAlexW2003874706

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.