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首页> 外文期刊>Clinical and Experimental Immunology: An Official Journal of the British Society for Immunology >Intravenous immunoglobulin does not increase FcγRIIB expression levels on monocytes in children with immune thrombocytopenia
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Intravenous immunoglobulin does not increase FcγRIIB expression levels on monocytes in children with immune thrombocytopenia

机译:静脉注射免疫球蛋白不会增加免疫性血小板减少症患儿单核细胞上的FcγRIIB表达水平

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摘要

Intravenous immunoglobulin (IVIG) produces a rapid and prolonged increase in the platelet counts of children with immune thrombocytopenia (ITP). The mechanism of IVIG efficacy in a murine model of ITP has been reported to operate through an IVIG-mediated increase in the expression of the inhibitory Fc receptor FcγRIIB(CD32B) on splenic macrophages. This investigation examined whether IVIG administration results in a similar increase in FcγRIIB expression on peripheral blood CD14 + monocytes in 20 children with ITP. FcγRIIB expression on peripheral blood monocytes was measured by flow cytometry in ITP patients, before and after IVIG therapy, as well as in control subjects. Peripheral blood monocytes were labelled with fluorescent-specific antibodies. There were no significant differences in the percentages or numbers of CD14 +CD32B + monocytes, or in the percentage of CD14 +CD32B + monocytes present in children with ITP before and after IVIG therapy. We suggest that IVIG does not increase FcγRIIB expression in peripheral blood monocytes in children with ITP.
机译:静脉内免疫球蛋白(IVIG)会导致免疫性血小板减少症(ITP)儿童的血小板计数快速且持续增加。据报道,在ITP鼠模型中IVIG功效的机制是通过IVIG介导的脾巨噬细胞上抑制性Fc受体FcγRIIB(CD32B)表达的增加而起作用的。这项研究检查了IVIG给药是否导致20例ITP儿童外周血CD14 +单核细胞上FcγRIIB表达的相似增加。通过流式细胞术在IVIG治疗之前和之后以及在对照受试者中通过流式细胞术来测量FcγRIIB在外周血单核细胞上的表达。用荧光特异性抗体标记外周血单核细胞。在IVIG治疗前后,ITP儿童中CD14 + CD32B +单核细胞的百分比或数量或CD14 + CD32B +单核细胞的百分比或数量无显着差异。我们建议IVIG不会增加ITP患儿外周血单核细胞中FcγRIIB的表达。

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