Evidence map›Paper›PMID 24558379›Full record

ArticlePloS one2014

Toll-like receptor 3 signalling up-regulates expression of the HIV co-receptor G-protein coupled receptor 15 on human CD4+ T cells.

Miriam Kiene, Bence Rethi, Marianne Jansson, Stephanie Dillon, Eric Lee, Rebecka Lantto, Cara Wilson, Stefan Pöhlmann, Francesca Chiodi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Activation of GPR15 and its involvement in the biological effects of smoking.Experimental biology and medicine (Maywood, N.J.) · 2017
    Review
  4. Article
  5. Review
  6. Article
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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

9 authors at 4 institutions in 3 countries.

Miriam KieneInstitute of Virology, Hannover Medical School, Hannover, Germany ; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Bence RethiDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Marianne JanssonDepartment of Laboratory Medicine, Lund University, Lund, Sweden.
Stephanie DillonDivision of Infectious Diseases, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
Eric LeeDivision of Infectious Diseases, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
Rebecka LanttoDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Cara WilsonDivision of Infectious Diseases, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
Stefan PöhlmannInfection Biology Unit, German Primate Center, Göttingen, Germany.
Francesca ChiodiDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Karolinska Institutet · SEUniversity of Colorado Anschutz Medical Campus · USGerman Primate Center · DELund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMany HIV-2 and SIV isolates, as well as some HIV-1 strains, can use the orphan 7-transmembrane receptor GPR15 as co-receptor for efficient entry into host cells. GPR15 is expressed on central memory and effector memory CD4(+) T cells in healthy individuals and a subset of these cells is susceptible to HIV-1 and SIV infection. However, it has not been determined whether GPR15 expression is altered in the context of HIV-1 infection.

resultsHere, we show that GPR15 expression in CD4(+) T cells is markedly up-regulated in some HIV-1 infected individuals compared to the rest of the infected patients and to healthy controls. Infection of the PM1 T cell line with primary HIV-1 isolates was found to up-regulate GPR15 expression on the infected cells, indicating that viral components can induce GPR15 expression. Up-regulation of GPR15 expression on CD4(+) T cells was induced by activation of Toll-like receptor 3 signalling via TIR-domain-containing adapter-inducing interferon-β (TRIF) and was more prominent on gut-homing compared to lymph node-homing CD4(+) T cells.

conclusionThese results suggest that infection-induced up-regulation of GPR15 expression could increase susceptibility of CD4(+) T cells to HIV infection and target cell availability in the gut in some infected individuals.

Indexed as

AdultAntigens, CD19BiopsyCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell SeparationColonFemaleFlow CytometryHIV-1HIV InfectionsHumansImmunologic MemoryLeukocytes, MononuclearMaleMiddle AgedAntigens, CD19GPR15 protein, humanReceptors, G-Protein-CoupledReceptors, PeptideTLR3 protein, humanToll-Like Receptor 3

Identifiers

PMID24558379
PMCPMC3928197
OpenAlexW2093755033

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.