CC chemokines and the receptors CCR3 and CCR5 are differentially expressed in the nonneoplastic leukocytic infiltrates of Hodgkin disease
Open Access
- 15 March 2001
- journal article
- Published by American Society of Hematology in Blood
- Vol. 97 (6) , 1543-1548
- https://doi.org/10.1182/blood.v97.6.1543
Abstract
Lymph nodes with Hodgkin disease (HD) harbor few neoplastic cells in a marked leukocytic infiltrate. Since chemokines are likely to be involved in the recruitmeKeywords
This publication has 32 references indexed in Scilit:
- High Expression of the CC Chemokine TARC in Reed-Sternberg CellsThe American Journal of Pathology, 1999
- Molecular cloning and characterization of a human eotaxin receptor expressed selectively on eosinophils.The Journal of Experimental Medicine, 1996
- Monocyte chemotactic protein 4 (MCP-4), a novel structural and functional analogue of MCP-3 and eotaxin.The Journal of Experimental Medicine, 1996
- Cloning, expression, and characterization of the human eosinophil eotaxin receptor.The Journal of Experimental Medicine, 1996
- RANTES and macrophage inflammatory protein 1 alpha selectively enhance immunoglobulin (IgE) and IgG4 production by human B cells.The Journal of Experimental Medicine, 1996
- Cloning of the human eosinophil chemoattractant, eotaxin. Expression, receptor binding, and functional properties suggest a mechanism for the selective recruitment of eosinophils.Journal of Clinical Investigation, 1996
- Human RANTES induces the migration of human T lymphocytes into the peripheral tissues of mice with severe combined immune deficiencyEuropean Journal of Immunology, 1994
- Eotaxin: a potent eosinophil chemoattractant cytokine detected in a guinea pig model of allergic airways inflammation.The Journal of Experimental Medicine, 1994
- Human macrophage inflammatory protein alpha (MIP-1 alpha) and MIP-1 beta chemokines attract distinct populations of lymphocytes.The Journal of Experimental Medicine, 1993
- A high proportion of T lymphocytes that infiltrate H-2-incompatible heart allografts in vivo express genes encoding cytotoxic cell-specific serine proteases, but do not express the MEL-14-defined lymph node homing receptor.The Journal of Experimental Medicine, 1988