Evidence map›Paper›PMID 24052528›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Superior induction and maintenance of protective CD8 T cells in mice infected with mouse cytomegalovirus vector expressing RAE-1γ.

Tihana Trsan, Andreas Busche, Maja Abram, Felix M Wensveen, Niels A Lemmermann, Maja Arapovic, Marina Babic, Adriana Tomic, Mijo Golemac, Melanie M Brinkmann and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  7. Review
  8. Article
  9. Article
  10. Review
  11. Vaccine vectors: the bright side of cytomegalovirus.Medical microbiology and immunology · 2019
    Review
  12. Brain-resident memory CD8European journal of immunology · 2018
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. NKG2D Receptor and Its Ligands in Host Defense.Cancer immunology research · 2015
    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

16 authors at 5 institutions in 3 countries.

Tihana TrsanDepartment of Histology and Embryology, Faculty of Medicine, University of Rijeka, 51000 Rijeka, Croatia.
Andreas Busche
Maja Abram
Felix M Wensveen
Niels A Lemmermann
Maja Arapovic
Marina Babic
Adriana Tomic
Mijo Golemac
Melanie M Brinkmann
Wiebke Jäger
Annette Oxenius
Bojan Polic
Astrid Krmpotic
Martin Messerle
Stipan Jonjic
University of Rijeka · HRMedizinische Hochschule Hannover · DEETH Zurich · CHHelmholtz Centre for Infection Research · DEJohannes Gutenberg University Mainz · DE

Funding

Viral evasion of NK cellsR01AI083201 · NIAID · UNIVERSITY OF RIJEKA--MEDICAL FACULTY · PI JONJIC, STIPAN · 2009 to 2012
$331k
NIAID NIH HHS 1R01AI083201-01NIAID NIH HHS R01 AI083201
6 · The paper itself

Abstract

Due to a unique pattern of CD8 T-cell response induced by cytomegaloviruses (CMVs), live attenuated CMVs are attractive candidates for vaccine vectors for a number of clinically relevant infections and tumors. NKG2D is one of the most important activating NK cell receptors that plays a role in costimulation of CD8 T cells. Here we demonstrate that the expression of CD8 T-cell epitope of Listeria monocytogenes by a recombinant mouse CMV (MCMV) expressing the NKG2D ligand retinoic acid early-inducible protein 1-gamma (RAE-1γ) dramatically enhanced the effectiveness and longevity of epitope-specific CD8 T-cell response and conferred protection against a subsequent challenge infection with Listeria monocytogenes. Unexpectedly, the attenuated growth in vivo of the CMV vector expressing RAE-1γ and its capacity to enhance specific CD8 T-cell response were preserved even in mice lacking NKG2D, implying additional immune function for RAE-1γ beyond engagement of NKG2D. Thus, vectors expressing RAE-1γ represent a promising approach in the development of CD8 T-cell-based vaccines.

Indexed as

AnimalsCD8-Positive T-LymphocytesCytomegalovirusFlow CytometryGenetic VectorsImmune EvasionListeria monocytogenesMembrane ProteinsMiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutNK Cell Lectin-Like Receptor Subfamily KStatistics, NonparametricVaccines, SyntheticKlrk1 protein, mouseMembrane ProteinsNK Cell Lectin-Like Receptor Subfamily KRaet1c protein, mouseVaccines, SyntheticCD8 T cell vaccineRAE-1 gammavaccine vector

Identifiers

PMID24052528
PMCPMC3799388
OpenAlexW2099149491

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.