Results 11 to 20 of about 10,033 (176)

Prevention and treatment of experimental autoimmune encephalomyelitis by soluble CD83. [PDF]

open access: yesJ Exp Med, 2004
CD83 is up-regulated on the surface of dendritic cells (DCs) during maturation and has been widely used as a marker for mature DCs. Recently, we reported the recombinant expression of the extracellular immunoglobulin domain of human CD83 (hCD83ext). Using this soluble form of CD83, allogeneic as well as specific cytotoxic T lymphocyte proliferation ...
Zinser E   +4 more
europepmc   +6 more sources

CD83: Activation Marker for Antigen Presenting Cells and Its Therapeutic Potential

open access: yesFrontiers in Immunology, 2019
CD83 is a member of the immunoglobulin (Ig) superfamily and is expressed in membrane bound or soluble forms. Membrane CD83 (mCD83) can be detected on a variety of activated immune cells, although it is most highly and stably expressed by mature dendritic
Ziduo Li   +13 more
doaj   +3 more sources

The CD83 Molecule – An Important Immune Checkpoint

open access: yesFrontiers in Immunology, 2020
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.
Linda Grosche   +9 more
doaj   +3 more sources

The soluble form of CD83 dramatically changes the cytoskeleton of dendritic cells

open access: yesImmunobiology, 2004
CD83 is the best-known surface marker for mature dendritic cells (DC) and recently we could show that a soluble form of CD83 inhibits DC maturation. In addition, this soluble form inhibits DC-mediated T cell proliferation in vitro and in vivo. Furthermore, several viruses induce CD83 degradation or shedding in infected DC.
Nicole, Kotzor   +3 more
openaire   +4 more sources

A limited course of soluble CD83 delays acute cellular rejection of MHC-mismatched mouse skin allografts [PDF]

open access: yesTransplant International, 2007
CD83 is a surface marker expressed on matured dendritic cells (DCs). It plays a pivotal role in the mediation of DC/T cell interaction and induction of T-cell activation. Previous studies have suggested that a soluble form of CD83 could suppress DC maturation and inhibit T-cell activation and, as a result, it can prevent paralysis associated with ...
Jun-Fa, Xu   +9 more
openaire   +4 more sources

Staphylococcal Enterotoxin A Shapes Monocyte Transcription and Macrophage Polarization: Implications for Immune Responses in Infection and Inflammation. [PDF]

open access: yesEur J Immunol
Staphylococcal enterotoxin A (SEA) alters monocyte differentiation and function, while preserving T cell stimulatory capacity. SEA‐primed macrophages downregulate antigen‐presenting markers yet drive heightened T‐cell proliferation and IFN‐γ secretion.
Arasa C   +4 more
europepmc   +2 more sources

Soluble CD83 inhibits acute rejection by up regulating TGF-β and IDO secretion in rat liver transplantation

open access: yesTransplant Immunology, 2021
Allogeneic transplantation immune tolerance is currently a hot research issue and soluble CD83(sCD83) is a novel immunomodulator with great potential in inducing transplantation tolerance.To investigate the mechanism of the immune tolerance effect of sCD83 on rat liver transplantation.A rat liver transplantation model was established to study the ...
Liangxing, Xiong   +5 more
openaire   +4 more sources

Alpha-toxin-elicited CX3CL1 release in Staphylococcus aureus pneumonia impairs bactericidal function of human monocytes [PDF]

open access: yesmBio
Staphylococcus aureus is an important human pathogen causing severe invasive infections. Pathogenesis is attributed to a wide array of virulence factors, including several potent exotoxins such as the pore-forming α-toxin.
Srikanth Mairpady Shambat   +20 more
doaj   +2 more sources

Chimeric Antigen Receptor T-Cell Therapy: More Than an Anti-Cancer Drug. [PDF]

open access: yesHLA
ABSTRACT Initially, chimeric antigen receptor (CAR) T‐cell therapy was developed to eliminate malignant B cells in haematological B‐cell malignancies by targeting CD19 and B‐cell maturation antigen. This approach achieved notable success, resulting in (malignant) B‐cell depletion and inducing clinical remission in cancer patients.
Schenk HCM   +8 more
europepmc   +2 more sources

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