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Published online before print November 29, 2004
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* Mater Medical Research Institute, South Brisbane, Queensland, Australia;
Institute of Pathology, Rikshospitalet, Oslo, Norway; and
Hematology/Immunology Research Group, Christchurch Hospital, New Zealand
1 Correspondence: Mater Medical Research Institute, Aubigny Place, Raymond Terrace, South Brisbane, Queensland, 4101, Australia. E-mail: svuckovic{at}mmri.mater.org.au
CD123hi CD11c dendritic cells (CD123hi DC) are a distinct subset of human DC present in bone marrow, blood, lymphoid organs, and peripheral tissues. Pathogen stimulation, cytokine, or CD40 ligation induces CD123hi DC maturation, involving a shift from their innate immune to cognate antigen-presenting functions. In this study, we revealed that blood CD123hi DC in the presence of cytokine (granulocyte macrophage-colony stimulating factor and interleukin-3) undergo progressive, step-wise maturation through an "early" stage, delineated by expression of the antigen detected by the new monoclonal antibody CMRF58 (CD123hiCMRF58+CD40CD86CD83) to the "late" stage with costimulatory antigen expression (CD123hiCMRF58+CD40+CD86+CD83+/). In this early stage, cytokine-maintained CD123hi DC do not display changes in their morphology, no longer produce interferon-
(IFN-
) in response to bacteria, and develop the capacity to induce proliferation and polarization of allogeneic T cells. CD123hiCMRF58+ DC, phenotypically similar to in vitro cytokine-maintained CD123hi DC, were not detected in tonsil but are present in allergen-challenged nasal mucosa of allergic individuals. Thus, CD123hi DC in certain tissue environments such as allergen-challenged nasal mucosa share a common CD123hiCMRF58+ phenotype with in vitro cytokine-maintained blood CD123hi DC characterized by lack of IFN-
production.
Key Words: CD123hi dendritic cells mAb CMRF58 nasal allergy
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