Evidence map›Paper›PMID 36830955›Full record

ArticleBiomedicines2023

TMPRSS2 Impacts Cytokine Expression in Murine Dendritic Cells.

Sandra Gunne, Marie Schwerdtner, Marina Henke, Ann-Kathrin Schneider, Lucas Keutmann, Eva Böttcher-Friebertshäuser, Susanne Schiffmann

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. 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
0.8field-weighted citation impact, top 26% 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, 5 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  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

7 authors at 2 institutions in 1 country.

Sandra GunneFraunhofer Institute for Translational Medicine and Pharmacology (ITMP), Theodor-Stern-Kai 7, 60596 Frankfurt am Main, Germany.ORCID 0000-0002-6492-6684
Marie SchwerdtnerInstitute of Virology, Philipps-University Marburg, 35043 Marburg, Germany.
Marina HenkeFraunhofer Institute for Translational Medicine and Pharmacology (ITMP), Theodor-Stern-Kai 7, 60596 Frankfurt am Main, Germany.ORCID 0000-0002-7661-5832
Ann-Kathrin SchneiderFraunhofer Institute for Translational Medicine and Pharmacology (ITMP), Theodor-Stern-Kai 7, 60596 Frankfurt am Main, Germany.
Lucas KeutmannFraunhofer Institute for Translational Medicine and Pharmacology (ITMP), Theodor-Stern-Kai 7, 60596 Frankfurt am Main, Germany.
Eva Böttcher-FriebertshäuserInstitute of Virology, Philipps-University Marburg, 35043 Marburg, Germany.ORCID 0000-0002-0007-8110
Susanne SchiffmannFraunhofer Institute for Translational Medicine and Pharmacology (ITMP), Theodor-Stern-Kai 7, 60596 Frankfurt am Main, Germany.ORCID 0000-0001-5035-2504
Fraunhofer Institute for Translational Medicine and Pharmacology · DEPhilipps University of Marburg · DE

Funding

BMBF project HELIATAR 16GW0260Fraunhofer Cluster of Excellence Immune mediated diseases (CIMD) not applicableLandesoffensive zur Entwicklung wissenschaft-lich-ökonomischer Exzellenz (LOEWE) Research Centre for Novel Drug Targets against Poverty-Related and Neglected Tropical Infectious Dis-eases (DRUID) not applicableLeistungszentrum innovative Therapeutics (TheraNova) not applicableLOEWE Centre for Personalized Translational Epilepsy Research (Cepter) not applicableLOEWE Centre for Translational Biodiversity Genomics not applicable
6 · The paper itself

Abstract

backgroundThe transmembrane protease serine 2 (TMPRSS2) proteolytically activates the envelope proteins of several viruses for viral entry via membrane fusion and is therefore an interesting and promising target for the development of broad-spectrum antivirals. However, the use of a host protein as a target may lead to potential side effects, especially on the immune system. We examined the effect of a genetic deletion of

methodsBone marrow cells from wild-type (WT) and TMPRSS2-deficient mice (TMPRSS2

resultsIn cDCs, the lack of TMPRSS2 led to an increase in IL12 and IFNγ in TLR7/8 agonist resiquimod or TLR 9 agonist ODN 1668-activated cells. Only IL-10 was reduced in TMPRSS2

conclusionThe effect of TMPRSS2 on pDCS and cDCs depends on the activated TLR, and TMPRSS2 seems to affect cytokine release differently in pDCs and cDCs. In cDCs, TMPRSS2 seems to suppress cytokine release, whereas in pDCS TMPRSS2 possibly mediates cytokine release.

Indexed as

cytokine secretiondendritic cellsinfectionTMPRSS2TMPRSS2-knockout mouse

Identifiers

PMID36830955
PMCPMC9952936
OpenAlexW4318824799

What OpenQuestion holds

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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.