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一般来说,囊性纤维化患者的血白细胞吞噬功能并未受损。

The Phagocytosis of Blood Leukocytes from Cystic Fibrosis Patients is not Impaired in General.

机构信息

Institute for Anatomy and Cell Biology, Saarland University, Campus Homburg, Kirrberger Strasse, Building 61, 66424, Homburg/Saar, Germany.

Clinic for Pulmonology, Saarland University, Campus Homburg, Homburg/Saar, Germany.

出版信息

Lung. 2020 Feb;198(1):235-239. doi: 10.1007/s00408-019-00290-9. Epub 2019 Nov 9.

Abstract

Impaired phagocytosis of Pseudomonas aeruginosa was found in isolated monocytes of peripheral blood of cystic fibrosis patients, but not in their neutrophils, as reported some years ago. In the present study, we analysed the phagocytic capacity of peripheral blood neutrophils and monocytes of cystic fibrosis patients and of healthy controls. Phagocytosis was determined using a commercial phagocytosis "in whole blood" assay on the basis of fluorescence-labelled opsonized Escherichia coli bacteria and flow cytometry. Venous blood of cystic fibrosis patients and of healthy controls was collected and the phagocytosis assay was performed. No differences in the percentage of phagocytic cells or in the overall phagocytic capacity were found between samples of cystic fibrosis patients and healthy controls either in monocytes or in neutrophils. Thus, our results did not support the hypothesis of a generally reduced phagocytic ability in the peripheral blood immune cells of cystic fibrosis patients.

摘要

一些年前的研究发现,囊性纤维化患者外周血中的分离单核细胞吞噬铜绿假单胞菌的能力受损,但中性粒细胞不受影响。在本研究中,我们分析了囊性纤维化患者和健康对照者外周血中性粒细胞和单核细胞的吞噬能力。吞噬作用是通过基于荧光标记的调理大肠杆菌细菌和流式细胞术的商业吞噬“全血”测定来确定的。收集囊性纤维化患者和健康对照者的静脉血,并进行吞噬作用测定。在单核细胞或中性粒细胞中,囊性纤维化患者和健康对照者的样本之间在吞噬细胞的百分比或整体吞噬能力方面均无差异。因此,我们的结果不支持囊性纤维化患者外周血免疫细胞普遍吞噬能力降低的假设。

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