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H. Terry Wepsic, M.D. Professor Emeritus M.D., Yale Medical School, 1968
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Current research interests involve the mechanisms through which macrophages can modulate the activities of the immune system. These cells can both enhance immune responses as well as inhibit immunity. We have previously identified that a cloned suppressor hybridoma cell line induces natural suppression through the release of a cytokine, macrophage colony stimulating factor (M-CSF). M-CSF activated macrophages suppressed lymphocytic responses through a non-apoptotic pathways. This animal model may be the first in vitro model of a human disease known as Rosai-Dorfman disease. Besides making a secreted form of M-CSF, our cell line possesses another isoform of M-CSF which resides on the membrane of the cell. Macrophages now have the ability to kill those tumor cells which possess. The hypothesis that we are testing is that tumor cells which possess membrane bound M-CSF are able to stimulate macrophages into killing those cells. Macrophages which have killed these tumor cells are now able to stimulate the host's immune system, there by creating a tumor vaccine.
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Copyright © 2003 The Department of Pathology, University of California.
All rights reserved.
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