Evidence map›Paper›PMID 19234186›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Preferential use of B7.2 and not B7.1 in priming of vaccinia virus-specific CD8 T cells.

Shahram Salek-Ardakani, Ramon Arens, Rachel Flynn, Alessandro Sette, Stephen P Schoenberger, Michael Croft

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Cowpox virus encodes a protein that binds B7.1 and B7.2 and subverts T cell costimulation.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. CD8Immunity · 2017
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 3 institutions in 2 countries.

Shahram Salek-ArdakaniDivision of Molecular Immunology, La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, San Diego, CA 92037, USA. ssalek@liai.org
Ramon Arens
Rachel Flynn
Alessandro Sette
Stephen P Schoenberger
Michael Croft
Center of Molecular Immunology (Cuba) · CUDevelopmental Studies Center · USLa Jolla Institute for Immunology · US

Funding

TRAIL-mediated regulation of T help for CTLR01CA081261 · NCI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SCHOENBERGER, STEPHEN PHILIP · 2000 to 2009
$2.7M
Programming of CD8+ T Cell Tolerance by B Cell APCR01AI076972 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SCHOENBERGER, STEPHEN PHILIP · 2007 to 2011
$2.5M
TNFR Members in T Cell Immunity to VacciniaR01AI067341 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2006 to 2010
$2.3M
T Cell Memory to Respiratory Viral InfectionsR21AI077079 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SALEK-ARDAKANI, SHAHRAM · 2007 to 2008
$515k
TNFR Members in T Cell Immunity to VacciniaR56AI067341 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2012 to 2012
$348k
NCI NIH HHS CA081261NCI NIH HHS R01 CA081261NIAID NIH HHS AI076972NIAID NIH HHS AI67341NIAID NIH HHS AI77079NIAID NIH HHS R01 AI067341NIAID NIH HHS R01 AI076972NIAID NIH HHS R21 AI077079NIAID NIH HHS R56 AI067341
6 · The paper itself

Abstract

Recent studies have demonstrated that CD28 provides critical costimulatory signals required for optimal CD8 T cell expansion and effector function in response to several viruses, including influenza, HSV, and vaccinia virus (VACV). CD28 has two ligands expressed largely on professional APC, named B7.1 (CD80) and B7.2 (CD86). Although some results suggest that these ligands are equivalent and both promote CD28 signaling, it is not clear whether they are equally important for priming of antiviral T cells. Herein we show that B7.2 is critical for early CD8 T cell responses to both dominant and subdominant VACV epitopes, correlating with its strong induction on CD8alpha(+) dendritic cells. In contrast, B7.1 plays no significant role. Signals from an exogenously applied adjuvant can recruit B7.1 activity and lead to further enhanced priming of VACV-reactive CD8 T cells. However, during a natural infection, B7.1 is not functional, likely related to inefficient up-regulation or active suppression by VACV. These studies provide evidence that B7.2 is the major ligand for the CD28 receptor on VACV-specific CD8 T cells, that B7.2 can promote efficient CD8 T cell priming without B7.1, and that B7.1 and B7.2 can be differentially utilized during antiviral responses.

Indexed as

Acute DiseaseAnimalsB7-1 AntigenB7-2 AntigenCD28 AntigensCD8 AntigensCD8-Positive T-LymphocytesCell DifferentiationCells, CulturedFemaleImmunodominant EpitopesLymphocyte ActivationMaleMiceMice, Inbred C57BLMice, KnockoutB7-1 AntigenB7-2 AntigenCD28 AntigensCD86 protein, humanCd86 protein, mouseCD8alpha antigenCD8 AntigensImmunodominant Epitopes

Identifiers

PMID19234186
PMCPMC2707928
OpenAlexW1700957225

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.