Evidence map›Paper›PMID 19876399›Full record

ArticlePloS one2009

Liver is able to activate naïve CD8+ T cells with dysfunctional anti-viral activity in the murine system.

John R Lukens, Joseph S Dolina, Taeg S Kim, Robert S Tacke, Young S Hahn

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  5. Liver-resident CD103+ dendritic cells prime antiviral CD8+ T cells in situ.Journal of immunology (Baltimore, Md. : 1950) · 2015
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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

5 authors at 1 institution in 1 country.

John R LukensBeirne Carter Center for Immunology Research, Department of Microbiology, University of Virginia, Charlottesville, Virginia, USA.
Joseph S Dolina
Taeg S Kim
Robert S Tacke
Young S Hahn
University of Virginia · US

Funding

Regulation of CD8+ T cell responses via liver NK-DC crosstalkU19AI083024 · NIAID · UNIVERSITY OF VIRGINIA · PI BRACIALE, THOMAS J · 2009 to 2013
$8.1M
UVA Digestive Health Research CenterP30DK067629 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI PIZARRO, THERESA TORRES · 2004 to 2008
$5.6M
Role of NK in Regulation of anti-viral T cell immunityR01DK063222 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI HAHN, YOUNG S. · 2003 to 2011
$2.0M
NIAID NIH HHS 5T32AI10749608.NIAID NIH HHS U19 AI083024NIAID NIH HHS U19AI083024NIDDK NIH HHS DK063222NIDDK NIH HHS P30 DK067629NIDDK NIH HHS R01 DK063222
6 · The paper itself

Abstract

The liver possesses distinct tolerogenic properties because of continuous exposure to bacterial constituents and nonpathogenic food antigen. The central immune mediators required for the generation of effective immune responses in the liver environment have not been fully elucidated. In this report, we demonstrate that the liver can indeed support effector CD8(+) T cells during adenovirus infection when the T cells are primed in secondary lymphoid tissues. In contrast, when viral antigen is delivered predominantly to the liver via intravenous (IV) adenovirus infection, intrahepatic CD8(+) T cells are significantly impaired in their ability to produce inflammatory cytokines and lyse target cells. Additionally, intrahepatic CD8(+) T cells generated during IV adenovirus infection express elevated levels of PD-1. Notably, lower doses of adenovirus infection do not rescue the impaired effector function of intrahepatic CD8(+) T cell responses. Instead, intrahepatic antigen recognition limits the generation of potent anti-viral responses at both priming and effector stages of the CD8(+) T cell response and accounts for the dysfunctional CD8(+) T cell response observed during IV adenovirus infection. These results also implicate that manipulation of antigen delivery will facilitate the design of improved vaccination strategies to persistent viral infection.

Indexed as

AdenoviridaeAdenoviridae InfectionsAnimalsAntiviral AgentsBone Marrow CellsCD8-Positive T-LymphocytesCell DifferentiationCoculture TechniquesCytokinesFlow CytometryLiverMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicSpleenAntiviral AgentsCytokines

Identifiers

PMID19876399
PMCPMC2764869
OpenAlexW2043356729

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.