Rheumatology Advance Access published online on November 30, 2004
Rheumatology, doi:10.1093/rheumatology/keh488
Rheumatology © British Society for Rheumatology 2004; all rights reserved
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1 Department of Pediatrics, Yamaguchi University School of Medicine, 1-1-1 Minami-kogushi, Ube, Yamaguchi 755-8505, Japan
* To whom correspondence should be addressed. Objectives. Intravenous immunoglobulin (IVIG) therapy has been reported to be effective for reducing the incidence of coronary artery lesions in Kawasaki disease (KD), an acute febrile vasculitis of unknown aetiology. Regarding the mechanism of IVIG in immune thrombocytopenic purpura (ITP), it has been reported that IVIG increases the expression of the inhibitory Fc receptor, Fc Methods. The expression of Fc Results. The percentage of CD14+CD32B+ monocytes/macrophages among peripheral blood mononuclear cells, the absolute number of CD14+CD32B+ monocytes/macrophages and the percentage of CD14+CD32B+ monocytes/macrophages among CD14+ monocytes/macrophages in patients with acute KD before IVIG therapy were significantly increased compared with those after IVIG therapy and in controls. CD14+CD32B+ monocytes/macrophages decreased to within the normal range soon after IVIG therapy. Conclusions. IVIG therapy in patients with KD did not increase the expression of Fc
Accepted October 19, 2004
Concise report
Intravenous immunoglobulin does not increase Fc
RIIB expression on monocytes/macrophages during acute Kawasaki disease
T. Ichiyama, E-mail: ichiyama{at}yamaguchi-u.ac.jp
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Abstract
RIIB (CD32B), on splenic macrophages in a murine ITP model. Regarding the mechanism of IVIG during acute KD, we investigated whether or not IVIG increases the expression of Fc
RIIB in peripheral blood CD14+ monocytes/macrophages.
RIIB in peripheral blood CD14+ monocytes/macrophages was determined before and after IVIG therapy in 13 patients with acute KD by flow cytometry.
RIIB in peripheral blood CD14+ monocytes/macrophages during the acute stage.
RIIB; Intravenous immunoglobulin.
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