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镰状细胞病中的单核细胞吞噬活性。

Monocyte phagocytic activity in sickle cell disease.

作者信息

Mendoza E, Gutgsell N, Temple J D, Issitt P

机构信息

William J. Harrington Center for Blood Diseases, University of Miami School of Medicine, Fla.

出版信息

Acta Haematol. 1991;85(4):199-201. doi: 10.1159/000204892.

Abstract

The phagocytic activity of peripheral blood monocytes from sickle cell disease patients and normal controls was studied using a monocyte monolayer assay. Phagocytosis of antibody-coated red cells by monocytes from patients in stable condition and in normal controls did not differ significantly (7.1 +/- 1.5 vs. 5.3 +/- 0.9%). However, monocytes from sickle cell disease patients during vasoocclusive crises demonstrated increased phagocytic activity compared to the normal controls (11.0 +/- 2.7 vs. 5.3 +/- 0.9%, p less than 0.025). Numerous defects in immune response have been described in association with sickle cell disease. However, monocyte phagocytic activity is not deficient and is not a factor in the predisposition to infections.

摘要

采用单核细胞单层分析法研究了镰状细胞病患者和正常对照者外周血单核细胞的吞噬活性。病情稳定的患者和正常对照者的单核细胞对抗体包被红细胞的吞噬作用无显著差异(分别为7.1±1.5%和5.3±0.9%)。然而,与正常对照相比,血管闭塞性危象期间镰状细胞病患者的单核细胞吞噬活性增强(分别为11.0±2.7%和5.3±0.9%,p<0.025)。已有许多与镰状细胞病相关的免疫反应缺陷被描述。然而,单核细胞吞噬活性并不缺乏,也不是易感染的因素。

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