Cutting Edge: Histamine Inhibits IFN-α Release from Plasmacytoid Dendritic Cells
Author(s) -
Alessandra Mazzoni,
Cynthia A. Leifer,
Gregory Mullen,
Margaret Kennedy,
Dennis M. Klinman,
David M. Segal
Publication year - 2003
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.170.5.2269
Subject(s) - histamine , plasmacytoid dendritic cell , tlr9 , immunology , receptor , cytokine , microbiology and biotechnology , biology , dendritic cell , cpg oligodeoxynucleotide , tumor necrosis factor alpha , antigen , endocrinology , gene , gene expression , biochemistry , dna methylation
Plasmacytoid dendritic cells (DC) are professional APC and a major source of type I IFN following viral infection. We previously showed that histamine alters the cytokine profiles of maturing monocyte-derived DC resulting in a change from Th1 to Th2 in their T cell polarizing function. In this study, we show that human plasmacytoid DC, activated by either CpG oligodeoxynucleotides or viral infection, also respond to histamine through H2 receptors, leading to a marked down-regulation of IFN-alpha and TNF-alpha and a moderate switch in their capacity to polarize naive T cells. Our findings provide an explanation for low levels of type I IFN frequently observed in atopic individuals.
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