Evidence map›Paper›PMID 31293592›Full record

ArticleFrontiers in immunology2019

Endogenous Expression of the Human CD83 Attenuates EAE Symptoms in Humanized Transgenic Mice and Increases the Activity of Regulatory T Cells.

Elisabeth Zinser, Ronald Naumann, Andreas B Wild, Julia Michalski, Andrea Deinzer, Lena Stich, Christine Kuhnt, Alexander Steinkasserer, Ilka Knippertz

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. CD83 Regulates the Immune Responses in Inflammatory Disorders.International journal of molecular sciences · 2023
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
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 2 institutions in 1 country.

Elisabeth ZinserDepartment of Immune Modulation, Universitätsklinikum Erlangen, Erlangen, Germany.
Ronald NaumannTransgenic Core Facility, Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Andreas B WildDepartment of Immune Modulation, Universitätsklinikum Erlangen, Erlangen, Germany.
Julia MichalskiDepartment of Immune Modulation, Universitätsklinikum Erlangen, Erlangen, Germany.
Andrea DeinzerDepartment of Immune Modulation, Universitätsklinikum Erlangen, Erlangen, Germany.
Lena StichDepartment of Immune Modulation, Universitätsklinikum Erlangen, Erlangen, Germany.
Christine KuhntDepartment of Immune Modulation, Universitätsklinikum Erlangen, Erlangen, Germany.
Alexander SteinkassererDepartment of Immune Modulation, Universitätsklinikum Erlangen, Erlangen, Germany.
Ilka KnippertzDepartment of Immune Modulation, Universitätsklinikum Erlangen, Erlangen, Germany.
Universitätsklinikum Erlangen · DEMax Planck Institute of Molecular Cell Biology and Genetics · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CD83 is a type I membrane protein and part of the immunoglobulin superfamily of receptors. CD83 is involved in the regulation of antigen presentation and dendritic cell dependent allogeneic T cell proliferation. A soluble form of CD83 inhibits dendritic cell maturation and function. Furthermore, CD83 is expressed on activated B cells, T cells, and in particular on regulatory T cells. Previous studies on murine CD83 demonstrated this molecule to be involved in several immune-regulatory processes, comprising that CD83 plays a key role in the development und function of different immune cells. In order to get further insights into the function of the human CD83 and to provide preclinical tools to guide the function of CD83/sCD83 for therapeutic purposes we generated Bacterial Artificial Chromosomes (BAC) transgenic mice. BACs are excellent tools for manipulating large DNA fragments and are utilized to engineer transgenic mice by pronuclear injection. Two different founders of BAC transgenic mice expressing human CD83 (BAC-hCD83

Indexed as

AnimalsAntigens, CDB-LymphocytesCD83 AntigenCD8-Positive T-LymphocytesEncephalomyelitis, Autoimmune, ExperimentalHumansImmunoglobulinsMembrane GlycoproteinsMiceMice, TransgenicSomatostatin-Secreting CellsT-Lymphocytes, RegulatoryAntigens, CDCD83 AntigenImmunoglobulinsMembrane GlycoproteinsB cellsCD83dendritic cellsEAEregulatory T cellsT cellstransgenic mice

Identifiers

PMID31293592
PMCPMC6603205
OpenAlexW2955252237

What OpenQuestion holds

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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.