The class A macrophage scavenger receptor (SR) binds an extraordinary wide range of ligands including bacterial pathogens and mediates macrophage adhesion. In the present study, SR knock-out mice were infected with
Babesia microti to clarify its role in host defense mechanisms against protozoan infection. Several aspects of the immunological responses of mice during infection were studied. In
B. microti infection, the packed cell volumes of SR-/- mice at 16-30 days after infection were significantly higher than those of SR+/+ mice, although the course of parasitemia was not different between these mice. Increase in spleen weights after infection were less obvious in SR-/- mice than in SR+/+ mice at 20 days after infection. Flow cytometric studies revealed that the decreases in the percentages of Thy1.2
+ as well as CD4
+ T cells in spleen after
B. microti infection were higher in SR+/+ mice than that in SR-/- mice, whereas there were no difference in the rates of B220
+ cells between SR-/- and SR+/+ mice. The peritoneal macrophages from SR+/+ mice exhibited higher phagocytic activity than those from SR-/- mice. These results indicate that scavenger receptor enhances immune responses and phagocytosis of parasitized erythrocytes, although it does not directly play an important role of protection against
B. microti infection.
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