Evidence map›Paper›PMID 22079983›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

Cutting edge: activation of virus-specific CD4 T cells throughout γ-herpesvirus latency.

Michael L Freeman, Claire E Burkum, Kathleen G Lanzer, Meghan K Jensen, Mushtaq Ahmed, Eric J Yager, Emilio Flaño, Gary M Winslow, David L Woodland, Marcia A Blackman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
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 5 institutions in 1 country.

Michael L FreemanTrudeau Institute, Saranac Lake, NY 12983, USA.
Claire E Burkum
Kathleen G Lanzer
Meghan K Jensen
Mushtaq Ahmed
Eric J Yager
Emilio Flaño
Gary M Winslow
David L Woodland
Marcia A Blackman
Trudeau Institute · USAlbany College of Pharmacy and Health Sciences · USNationwide Children's Hospital · USNew York State Department of Health · USUniversity of Pittsburgh · US

Funding

T CELL IMMUNITY TO MHV 68, A MURINE GAMMA HERPEVIRUSR01AI042927 · NIAID · TRUDEAU INSTITUTE, INC. · PI BLACKMAN, MARCIA A · 1998 to 2008
$2.5M
Research Training in Immunology and Infectious DiseasesT32AI049823 · NIAID · TRUDEAU INSTITUTE, INC. · PI COOPER, ANDREA M · 2001 to 2015
$2.1M
Immunogenicity and efficacy of genetically engineered gamma-herpesvirus vaccinesRC2CA148250 · NCI · TRUDEAU INSTITUTE, INC. · PI BLACKMAN, MARCIA A, SUN, REN · 2009 to 2010
$1000k
Can persistent gamma-herpesviruses be purged from the host?R21AI082919 · NIAID · TRUDEAU INSTITUTE, INC. · PI BLACKMAN, MARCIA A · 2009 to 2010
$502k
CD* T cell responses to gamma-herpesviral infectionF32AI084327 · NIAID · TRUDEAU INSTITUTE, INC. · PI FREEMAN, MICHAEL L · 2009 to 2010
$98k
NCI NIH HHS CA148250NCI NIH HHS RC2 CA148250NIAID NIH HHS AI042927NIAID NIH HHS AI082919NIAID NIH HHS F32 AI084327NIAID NIH HHS R01 AI042927NIAID NIH HHS R21 AI082919NIAID NIH HHS T32 AI049823
6 · The paper itself

Abstract

CD4 T cells are essential for immune control of γ-herpesvirus latency. We previously identified a murine MHC class II-restricted epitope in γ-herpesvirus-68 gp150 (gp150(67-83)I-A(b)) that elicits CD4 T cells that are maintained throughout long-term infection. However, it is unknown whether naive cells can be recruited into the antiviral CD4 T cell pool during latency. In this study, we generate a mouse transgenic for a gp150-specific TCR and show epitope-specific activation of transgenic CD4 T cells during acute and latent infections. Furthermore, although only dendritic cells can stimulate virus-specific CD8 T cells during latency, we show that both dendritic cells and B cells stimulate transgenic CD4 T cells. These studies demonstrate that naive CD4 T cells specific for a viral glycoprotein can be stimulated throughout infection, even during quiescent latency, suggesting that CD4 T cell memory is maintained in part by the continual recruitment of naive cells.

Indexed as

AnimalsCD4-Positive T-LymphocytesCells, CulturedEpitopes, T-LymphocyteHerpesviridae InfectionsLymphocyte ActivationMiceMice, Inbred C57BLMice, TransgenicReceptors, Antigen, T-CellRhadinovirusVirus ActivationVirus LatencyEpitopes, T-LymphocyteReceptors, Antigen, T-Cell

Identifiers

PMID22079983
PMCPMC3237949
OpenAlexW2110002858

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.