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1



* Micromet AG, Munich, Germany;
Institute for Pathology, Technical University of Dresden, Dresden, Germany;
Institute for Pathology, University of Wurzburg, Wurzburg, Germany; Departments of
Surgery and
¶ Internal Medicine II, University of Munich, Munich, Germany
Recently, a new class of human dendritic cell (DC) precursors has been described in the peripheral blood recognized by the mAb M-DC8. These cells represent
1% of PBMC and acquire several characteristics of myeloid DC upon in vitro culture. In this report we show that M-DC8+ monocytes secrete in response to LPS >10 times the amount of TNF-
as M-DC8- monocytes, but produce significantly less IL-10. Consistent with a role in inflammatory responses, we found that M-DC8+ cells localized in the T cell area of inflamed human tonsils and in the subepithelial dome region of Peyers patches. In patients with active Crohns disease, abundant M-DC8+ cells were detectable in inflamed ileal mucosa, which were entirely depleted after systemic steroid treatment. Our results indicate that M-DC8+ cells are cells of DC phenotype in inflamed mucosa-associated lymphoid tissue that may contribute to the high level of TNF-
production in Crohns disease. We infer that selective elimination of M-DC8+ cells in inflammatory diseases has therapeutic potential.
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