| Literature DB >> 16782032 |
Knut Schäkel1, Matthias von Kietzell2, Anja Hänsel2, Annette Ebling2, Livia Schulze2, Michael Haase3, Christian Semmler4, Marika Sarfati5, A Neil Barclay6, Gwendalyn J Randolph7, Michael Meurer4, E Peter Rieber2.
Abstract
Early and high-level production of IL-12 is crucial for effective immune responses against pathogens. Up until now, the cells providing this initial IL-12 have remained elusive. Here we show that a subset of human blood dendritic cells (DC) is the principal and primary source of IL-12p70 when blood leukocytes are stimulated with the TLR4-ligand LPS or with CD40-ligand. These so-called slanDC are characterized by the 6-sulfo LacNAc modification of PSGL-1, which is identified by the mAb M-DC8. The IL-12 response of slanDC requires a few hours of in vitro maturation, which is completely blocked in the presence of erythrocytes. This inhibition of maturation depends on the expression of CD47 on erythrocytes and of its ligand SIRPalpha on DC. While strictly controlled in the blood by erythrocytes, the high IL-12- and TNF-alpha-producing capacity of slanDC in tissues may be critical in fighting off pathogens; if uncontrolled, it may lead to adverse inflammatory reactions.Entities:
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Year: 2006 PMID: 16782032 DOI: 10.1016/j.immuni.2006.03.020
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745