Evidence map›Paper›PMID 25225666›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Prolonged antigen presentation following an acute virus infection requires direct and then cross-presentation.

Erica L Heipertz, Michael L Davies, Eugene Lin, Christopher C Norbury

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Direct Priming of CD8Journal of virology · 2021
    Article
  7. Article
  8. Article
  9. Activation and trafficking of CD8Current opinion in virology · 2018
    Review
  10. Review
  11. Article
  12. The role of cDC1sF1000Research · 2017
    Review
  13. Article
  14. 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

4 authors at 1 institution in 1 country.

Erica L HeipertzDepartment of Microbiology and Immunology, Pennsylvania State University Milton S. Hershey Medical Center, Hershey, PA 17033.
Michael L DaviesDepartment of Microbiology and Immunology, Pennsylvania State University Milton S. Hershey Medical Center, Hershey, PA 17033.
Eugene LinDepartment of Microbiology and Immunology, Pennsylvania State University Milton S. Hershey Medical Center, Hershey, PA 17033.
Christopher C NorburyDepartment of Microbiology and Immunology, Pennsylvania State University Milton S. Hershey Medical Center, Hershey, PA 17033 cnorbury@hmc.psu.edu.
Penn State Milton S. Hershey Medical Center · US

Funding

The innate Immune Response to Mousepox at the Site - Associated ProjectU19AI083008 · NIAID · RESEARCH INST OF FOX CHASE CAN CTR · PI SIGAL, LUIS J · 2009 to 2013
$9.6M
VIRUSES AND CANCERT32CA060395 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI MEYERS, CRAIG M · 1994 to 2021
$4.3M
Pathways of Antigen Presentation to CD8 T Cells In VivoR01AI056094 · NIAID · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI NORBURY, CHRISTOPHER C · 2003 to 2013
$3.1M
Leukotrienes in Innate and Adaptive Antiviral ImmunityR01AI070537 · NIAID · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI NORBURY, CHRISTOPHER C · 2006 to 2009
$1.4M
Viral Manipulation of Myeloid Cell FunctionR21AI097787 · NIAID · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI NORBURY, CHRISTOPHER C · 2012 to 2013
$421k
Pathways of Antigen Presentation to CD8 T Cells In VivoR56AI056094 · NIAID · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI NORBURY, CHRISTOPHER C · 2008 to 2008
$384k
NCI NIH HHS 5 T32 CA60395-15NCI NIH HHS T32 CA060395NIAID NIH HHS AI 056094NIAID NIH HHS AI070537NIAID NIH HHS R01 AI056094NIAID NIH HHS R01 AI070537NIAID NIH HHS R21 AI097787NIAID NIH HHS R56 AI056094NIAID NIH HHS U19 AI083008
6 · The paper itself

Abstract

Antiviral CD8(+) T cell recognition of MHC class I-peptide complexes on the surface of professional APCs is a requisite step in an effective immune response following many potentially lethal infections. Although MHC class I-peptide production is thought to be closely linked to the continued presence of virus, several studies have shown that the persistence of Ag presentation occurs for an extended period of time following the clearance of RNA viruses. However, the mechanism responsible for Ag presentation persistence following viral clearance was unknown until now. In this study, we used a recombinant DNA virus expressing different forms of a model Ag to study the mechanism of prolonged Ag presentation in mice. We determined that the persistence of Ag presentation consists of three distinct mechanistic phases, as follows: ongoing viral replication, persistence of virally infected cells, and cross-presentation of Ag. These data will allow manipulation of the form of Ag contained within viral vectors to produce the most effective and protective CD8(+) T cell response to be generated following vaccination.

Indexed as

AnimalsAntigen PresentationAntigen-Presenting CellsAntigens, ViralCD8-Positive T-LymphocytesCells, CulturedCross-PrimingHistocompatibility Antigens Class ILymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutOvalbuminRecombinant ProteinsVaccinia virusVirus ReplicationAntigens, ViralHistocompatibility Antigens Class IOvalbuminRecombinant Proteins

Identifiers

PMID25225666
PMCPMC4305442
OpenAlexW2125098387

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.