CD83-stimulated monocytes suppress T-cell immune responses through production of prostaglandin E2.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 22065790.
- Also identified by DOI 10.1073/pnas.1018994108 and PMC identifier 3219128.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
CD83 is commonly known as a specific marker for mature dendritic cells. It has been shown to be important for CD4(+) T-cell development in the thymus. However, its function in the peripheral immune system remains enigmatic. Here, we show that CD83 inhibits proliferation and production of IL-2 and IFN-γ by T cells, and the inhibitory effect of CD83 is mediated by monocytes. Prostaglandin E2 (PGE(2)), but not IL-10 or TGF-β, was up-regulated specifically by CD83 in monocytes. Consistent with high levels of PGE(2), expression of COX-2 also was increased upon CD83 treatment. NF-κB activation also is required for induction of PGE(2) by CD83. Finally, application of the COX-2-selective inhibitor NS-398 fully prevented CD83-triggered inhibition of T-cell responses. Our study establishes an immune-regulatory mechanism by CD83 via stimulation of PGE(2) production in monocytes.
Medical subject headings
- Antigens, CD
- Dinoprostone
- Immunoglobulins
- Membrane Glycoproteins
- Monocytes
- T-Lymphocytes