The CD83 Molecule – An Important Immune Checkpoint

The CD83 molecule has been identified to be expressed on numerous activated immune cells, including B and T lymphocytes, monocytes, dendritic cells, microglia, and neutrophils. Both isoforms of CD83, the membrane-bound as well as its soluble form are topic of intensive research investigations. Sever...

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Main Authors: Linda Grosche, Ilka Knippertz, Christina König, Dmytro Royzman, Andreas B. Wild, Elisabeth Zinser, Heinrich Sticht, Yves A. Muller, Alexander Steinkasserer, Matthias Lechmann
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-04-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2020.00721/full
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spelling doaj-fb3c408893074d5eb6e59205ef14a1752020-11-25T02:27:49ZengFrontiers Media S.A.Frontiers in Immunology1664-32242020-04-011110.3389/fimmu.2020.00721534103The CD83 Molecule – An Important Immune CheckpointLinda Grosche0Ilka Knippertz1Christina König2Dmytro Royzman3Andreas B. Wild4Elisabeth Zinser5Heinrich Sticht6Yves A. Muller7Alexander Steinkasserer8Matthias Lechmann9Department of Immune Modulation, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, GermanyDepartment of Immune Modulation, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, GermanyDepartment of Immune Modulation, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, GermanyDepartment of Immune Modulation, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, GermanyDepartment of Immune Modulation, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, GermanyDepartment of Immune Modulation, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, GermanyDivision of Bioinformatics, Institute of Biochemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, GermanyDivision of Biotechnology, Department of Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, GermanyDepartment of Immune Modulation, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, GermanyDepartment of Immune Modulation, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, GermanyThe CD83 molecule has been identified to be expressed on numerous activated immune cells, including B and T lymphocytes, monocytes, dendritic cells, microglia, and neutrophils. Both isoforms of CD83, the membrane-bound as well as its soluble form are topic of intensive research investigations. Several studies revealed that CD83 is not a typical co-stimulatory molecule, but rather plays a critical role in controlling and resolving immune responses. Moreover, CD83 is an essential factor during the differentiation of T and B lymphocytes, and the development and maintenance of tolerance. The identification of its interaction partners as well as signaling pathways have been an enigma for the last decades. Here, we report the latest data on the expression, structure, and the signaling partners of CD83. In addition, we review the regulatory functions of CD83, including its striking modulatory potential to maintain the balance between tolerance versus inflammation during homeostasis or pathologies. These immunomodulatory properties of CD83 emphasize its exceptional therapeutic potential, which has been documented in specific preclinical disease models.https://www.frontiersin.org/article/10.3389/fimmu.2020.00721/fullCD83immune toleranceautoimmunityviral escape mechanismTreg cells
collection DOAJ
language English
format Article
sources DOAJ
author Linda Grosche
Ilka Knippertz
Christina König
Dmytro Royzman
Andreas B. Wild
Elisabeth Zinser
Heinrich Sticht
Yves A. Muller
Alexander Steinkasserer
Matthias Lechmann
spellingShingle Linda Grosche
Ilka Knippertz
Christina König
Dmytro Royzman
Andreas B. Wild
Elisabeth Zinser
Heinrich Sticht
Yves A. Muller
Alexander Steinkasserer
Matthias Lechmann
The CD83 Molecule – An Important Immune Checkpoint
Frontiers in Immunology
CD83
immune tolerance
autoimmunity
viral escape mechanism
Treg cells
author_facet Linda Grosche
Ilka Knippertz
Christina König
Dmytro Royzman
Andreas B. Wild
Elisabeth Zinser
Heinrich Sticht
Yves A. Muller
Alexander Steinkasserer
Matthias Lechmann
author_sort Linda Grosche
title The CD83 Molecule – An Important Immune Checkpoint
title_short The CD83 Molecule – An Important Immune Checkpoint
title_full The CD83 Molecule – An Important Immune Checkpoint
title_fullStr The CD83 Molecule – An Important Immune Checkpoint
title_full_unstemmed The CD83 Molecule – An Important Immune Checkpoint
title_sort cd83 molecule – an important immune checkpoint
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2020-04-01
description The CD83 molecule has been identified to be expressed on numerous activated immune cells, including B and T lymphocytes, monocytes, dendritic cells, microglia, and neutrophils. Both isoforms of CD83, the membrane-bound as well as its soluble form are topic of intensive research investigations. Several studies revealed that CD83 is not a typical co-stimulatory molecule, but rather plays a critical role in controlling and resolving immune responses. Moreover, CD83 is an essential factor during the differentiation of T and B lymphocytes, and the development and maintenance of tolerance. The identification of its interaction partners as well as signaling pathways have been an enigma for the last decades. Here, we report the latest data on the expression, structure, and the signaling partners of CD83. In addition, we review the regulatory functions of CD83, including its striking modulatory potential to maintain the balance between tolerance versus inflammation during homeostasis or pathologies. These immunomodulatory properties of CD83 emphasize its exceptional therapeutic potential, which has been documented in specific preclinical disease models.
topic CD83
immune tolerance
autoimmunity
viral escape mechanism
Treg cells
url https://www.frontiersin.org/article/10.3389/fimmu.2020.00721/full
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