Evidence map›Paper›PMID 19426216›Full record

ReviewImmunological reviews2009

Yin-Yang of costimulation: crucial controls of immune tolerance and function.

Roza I Nurieva, Xikui Liu, Chen Dong

Abstract readReview
In one paragraph

Review in Immunological reviews, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
–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

70 citing papers in PubMed, 1 synthesis or guideline pooled it.

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10 more citing papers are in PubMed but not listed here.

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

3 authors.

Roza I NurievaDepartment of Immunology, MD Anderson Cancer Center, Houston, TX, USA.
Xikui Liu
Chen Dong

Funding

Regulation of T cell activation and tolerance by GrailR01AI083761 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI NURIEVA, ROZA INSAFETDINOVNA · 2009 to 2013
$1.9M
NIAID NIH HHS R01 AI083761
6 · The paper itself

Abstract

summaryIn addition to signals from the T-cell receptor complex, it has been recognized for many years that a 'second' signal, most notably from CD28, is also important in T-cell activation. In the recent years, many new members of CD28 family as well as the molecules that share structural homology to CD28 ligands CD80 and CD86 have been discovered. Interestingly, some of these proteins function to dampen T-cell activation and regulate the induction of T-cell tolerance. Therefore, positive and negative costimulation are the two sides of the coin to fine tune T-cell receptor signaling to determine the outcome of T-cell receptor engagement-tolerance versus function.

Indexed as

Immune ToleranceLymphocyte ActivationAnimalsAntibody FormationAntigens, CDAntigens, Differentiation, T-LymphocyteApoptosis Regulatory ProteinsAutoimmunityB7-1 AntigenB7 AntigensCD28 AntigensHumansInducible T-Cell Co-Stimulator ProteinReceptors, Antigen, T-CellReceptors, ImmunologicSignal TransductionAntigens, CDAntigens, Differentiation, T-LymphocyteApoptosis Regulatory ProteinsB7-1 AntigenB7 AntigensCD276 protein, humanCD28 AntigensICOS protein, humanInducible T-Cell Co-Stimulator ProteinReceptors, Antigen, T-CellReceptors, Immunologic

Identifiers

PMID19426216
PMCPMC2875245

What OpenQuestion holds

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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.