Title | Coincident expression of the chemokine receptors CCR6 and CCR7 by pathologic Langerhans cells in Langerhans cell histiocytosis. |
Publication Type | Journal Article |
Year of Publication | 2003 |
Authors | Fleming MD, Pinkus JL, Fournier MV, Alexander SW, Tam C, Loda M, Sallan SE, Nichols KE, Carpentieri DF, Pinkus GS, Rollins BJ |
Journal | Blood |
Volume | 101 |
Issue | 7 |
Pagination | 2473-5 |
Date Published | 2003 Apr 01 |
ISSN | 0006-4971 |
Keywords | Chemokine CCL20, Chemokines, CC, Chemotaxis, Histiocytosis, Langerhans-Cell, Humans, Immunohistochemistry, Keratinocytes, Langerhans Cells, Macrophage Inflammatory Proteins, Macrophages, Osteoblasts, Receptors, CCR6, Receptors, CCR7, Receptors, Chemokine |
Abstract | It has been suggested that a switch in chemokine receptor expression underlies Langerhans cell migration from skin to lymphoid tissue. Activated cells are thought to down-regulate CCR6, whose ligand macrophage inflammatory protein-3 alpha (MIP-3 alpha)/CCL20 is expressed in skin, and up-regulate CCR7, whose ligands are in lymphoid tissues. In Langerhans cell histiocytosis (LCH), pathologic Langerhans cells (LCs) accumulate in several tissues, including skin, bone, and lymphoid organs. We have examined 24 LCH cases and find that pathologic LCs expressed CCR6 and CCR7 coincidentally in all cases. Furthermore, MIP-3 alpha/CCL20 is expressed by keratinocytes in involved skin and by macrophages and osteoblasts in involved bone. Expression of CCR6 by pathologic LCs may contribute to their accumulation in nonlymphoid organs such as skin and bone, whereas CCR7 expression may direct them to lymphoid tissue. Histiocytes in Rosai-Dorfman disease and hemophagocytic syndrome also coexpressed CCR6 and CCR7, suggesting that this may be a general attribute of abnormal histiocytes. |
DOI | 10.1182/blood.V101.7.2473 |
Alternate Journal | Blood |
PubMed ID | 12642342 |
Grant List | AI50225 / AI / NIAID NIH HHS / United States CA53091 / CA / NCI NIH HHS / United States |
Related Faculty:
Massimo Loda, M.D.