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Infection and Immunity, April 2005, p. 2559-2563, Vol. 73, No. 4
0019-9567/05/$08.00+0 doi:10.1128/IAI.73.4.2559-2563.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Department of Medicine,1 McLaughlin-Rotman Center for Global Health, McLaughlin Center for Molecular Medicine, University of Toronto,2 Tropical Disease Unit, Toronto General Hospital, Toronto, Ontario, Canada3
Received 13 September 2004/ Returned for modification 13 October 2004/ Accepted 2 December 2004
Ring-stage parasitized erythrocytes (RPEs) were demonstrated to interact with effector cells of the innate immune system. With receptor blockade studies and CD36-null macrophages, human and murine macrophages were shown to phagocytose RPEs through the pattern recognition receptor CD36. These in vitro data implicate scavenger receptors in the clearance of RPEs.
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