Evidence map›Paper›PMID 30781494›Full record

ArticleInternational journal of molecular sciences2019

hCMV-Mediated Immune Escape Mechanisms Favor Pathogen Growth and Disturb the Immune Privilege of the Eye.

Katrin Spekker-Bosker, Christoph-Martin Ufermann, Marco Maywald, Albert Zimmermann, Andreas Domröse, Claudia Woite, Walter Däubener, Silvia Kathrin Eller

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Glutaminolysis of CD4Journal of inflammation research · 2024
    Review
  3. Article
  4. 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

8 authors at 2 institutions in 1 country.

Katrin Spekker-BoskerInstitute of Medical Microbiology and Hospital Hygiene, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany. Spekker@uni-duesseldorf.de.
Christoph-Martin UfermannInstitute of Medical Microbiology and Hospital Hygiene, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany. Christoph-Martin.Ufermann@hhu.de.ORCID 0000-0002-4779-5424
Marco MaywaldInstitute of Virology, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany. marcomaywald@yahoo.de.
Albert ZimmermannInstitute of Virology, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany. Albert.Zimmermann@med.uni-duesseldorf.de.
Andreas DomröseInstitute of Medical Microbiology and Hospital Hygiene, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany. Andreas.Domroese@hhu.de.
Claudia WoiteInstitute of Medical Microbiology and Hospital Hygiene, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany. Claudia.Woite@hhu.de.
Walter DäubenerInstitute of Medical Microbiology and Hospital Hygiene, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany. daeubene@uni-duesseldorf.de.
Silvia Kathrin EllerInstitute of Medical Microbiology and Hospital Hygiene, Heinrich-Heine-University Düsseldorf, 40225 Düsseldorf, Germany. silvia.eller@uni-duesseldorf.de.
Heinrich Heine University Düsseldorf · DEBavarian Nordic (Germany) · DE

Funding

Jürgen Manchot Stiftung MOI III
6 · The paper itself

Abstract

Human retinal pigment epithelial (hRPE) cells are important for the establishment and maintenance of the immune privilege of the eye. They function as target cells for human cytomegalovirus (hCMV), but are able to restrict viral replication. hCMV causes opportunistic posterior uveitis such as retinitis and chorioretinitis. Both mainly occur in severely immunocompromised patients and rarely manifest in immunocompetent individuals. In this study, hRPE cells were infected with hCMV in vitro and activated with proinflammatory cytokines. The enzymatic activities of indoleamine 2,3-dioxygenase-1 (IDO1) and inducible nitric oxide synthase (iNOS) were determined. The antimicrobial capacity of both molecules was analyzed in co-infection experiments using

Indexed as

Cell ProliferationCoinfectionCytomegalovirusEyeFlow CytometryHumansImmune PrivilegeIndoleamine-Pyrrole 2,3,-DioxygenaseInterferon-gammaNitric Oxide Synthase Type IIRetinal Pigment EpitheliumStaphylococcus aureusT-LymphocytesToxoplasmaUveitisIDO1 protein, humanIndoleamine-Pyrrole 2,3,-DioxygenaseInterferon-gammaNitric Oxide Synthase Type IIchorioretinitishuman cytomegalovirushuman retinal pigment epithelial cellsIndoleamine 2,3-dioxygenase-1inducible nitric oxide synthaseocular toxoplasmosisretinitisStaphylococcus aureusToxoplasma gondiiuveitis

Identifiers

PMID30781494
PMCPMC6413209
OpenAlexW2914231894

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.