Evidence map›Paper›PMID 22491458›Full record

ArticleJournal of virology2012

Suppression of antigen-specific T cell responses by the Kaposi's sarcoma-associated herpesvirus viral OX2 protein and its cellular orthologue, CD200.

Karen Misstear, Simon A Chanas, S A Rahim Rezaee, Rachel Colman, Laura L Quinn, Heather M Long, Oliver Goodyear, Janet M Lord, Andrew D Hislop, David J Blackbourn

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 45 citations in OpenAlex.

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  12. KSHV: Immune Modulation and Immunotherapy.Frontiers in immunology · 2019
    Review
  13. Article
  14. Centrin-DeletedFrontiers in immunology · 2018
    Article
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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

10 authors at 3 institutions in 2 countries.

Karen MisstearSchool of Cancer Sciences, CR UK Centre for Cancer Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom.
Simon A Chanas
S A Rahim Rezaee
Rachel Colman
Laura L Quinn
Heather M Long
Oliver Goodyear
Janet M Lord
Andrew D Hislop
David J Blackbourn
Immune Regulation (United Kingdom) · GBMashhad University of Medical Sciences · IRUniversity of Birmingham · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/B/14442Cancer Research UK C7934Medical Research Council G0400408Medical Research Council G0501074Medical Research Council G0800154
6 · The paper itself

Abstract

Regulating appropriate activation of the immune response in the healthy host despite continual immune surveillance dictates that immune responses must be either self-limiting and therefore negatively regulated following their activation or prevented from developing inappropriately. In the case of antigen-specific T cells, their response is attenuated by several mechanisms, including ligation of CTLA-4 and PD-1. Through the study of the viral OX2 (vOX2) immunoregulator encoded by Kaposi's sarcoma-associated herpesvirus (KSHV), we have identified a T cell-attenuating role both for this protein and for CD200, a cellular orthologue of the viral vOX2 protein. In vitro, antigen-presenting cells (APC) expressing either native vOX2 or CD200 suppressed two functions of cognate antigen-specific T cell clones: gamma interferon (IFN-γ) production and mobilization of CD107a, a cytolytic granule component and measure of target cell killing ability. Mechanistically, vOX2 and CD200 expression on APC suppressed the phosphorylation of ERK1/2 mitogen-activated protein kinase in responding T cells. These data provide the first evidence for a role of both KSHV vOX2 and cellular CD200 in the negative regulation of antigen-specific T cell responses. They suggest that KSHV has evolved to harness the host CD200-based mechanism of attenuation of T cell responses to facilitate virus persistence and dissemination within the infected individual. Moreover, our studies define a new paradigm in immune modulation by viruses: the provision of a negative costimulatory signal to T cells by a virus-encoded orthologue of CD200.

Indexed as

Immune ToleranceAntigen-Presenting CellsAntigens, CDHerpesvirus 8, HumanHumansInterferon-gammaLysosomal-Associated Membrane Protein 1Orexin ReceptorsReceptors, G-Protein-CoupledReceptors, NeuropeptideT-LymphocytesViral ProteinsVirulence FactorsAntigens, CDantigens, CD200Interferon-gammaLysosomal-Associated Membrane Protein 1Orexin ReceptorsReceptors, G-Protein-CoupledReceptors, NeuropeptideViral ProteinsVirulence Factors

Identifiers

PMID22491458
PMCPMC3372194
OpenAlexW2067488876

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.