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慢性透析患者中性粒细胞和单核细胞趋化因子诱导反应的改变。

Alterations in chemotactic factor-induced responses of neutrophils and monocytes from chronic dialysis patients.

作者信息

Lewis S L, Van Epps D E, Chenoweth D E

机构信息

Department of Pathology, University of New Mexico, Albuquerque 87131.

出版信息

Clin Nephrol. 1988 Aug;30(2):63-72.

PMID:2846218
Abstract

Chronic renal failure patients on dialysis have an increased susceptibility to infection. Previous studies have demonstrated that these patients have a decreased in vitro neutrophil (PMN) chemotactic response and a reduction in C5a receptor availability on both PMN and monocytes. This study was designed to determine if other chemotactic factor-mediated responses of PMN and monocytes from hemodialysis (HD) and continuous ambulatory peritoneal dialysis (CAPD) patients are abnormal. The responses investigated included in vitro chemotaxis, superoxide generation, H2O2 production, and myeloperoxidase (MPO) release. These studies showed that PMN from HD and CAPD patients are significantly decreased in their chemotactic response to both C5a and fMLP when compared to normal controls. The response of HD patient's PMN to C5a was decreased by an average of 55.1% (p less than 0.005) and for CAPD patients by 49.7% (p less than 0.01). Similarly, chemotactic responses to fMLP were decreased by an average of 44.7% (p less than 0.005) for HD patients and 36.3% (p less than 0.02) for CAPD patients. Superoxide anion production by PMN and monocytes from HD and CAPD patients in response to C5a and fMLP was also significantly decreased compared to controls. PMN superoxide production in response to C5a was decreased by an average of 36.5% (p less than 0.001) for HD patients and 32.0% (p less than 0.001) for CAPD patients. fMLP-stimulated production of superoxide was also decreased but to a lesser degree with a mean decrease of 18.0% (p less than 0.01) for HD patients and 24.1% decrease (p less than 0.01) for CAPD patients. This decreased responsiveness was restricted to C5a- and fMLP-stimulated superoxide production since phorbol myristate acetate (PMA)-stimulated responses were comparable to controls. A similar pattern of decreased superoxide production was found with monocytes from these patients. Comparable decreases in chemotactic factor-stimulated responses were also observed in a flow cytometric assay of H2O2 production in both PMN and monocytes and an in vitro assay of MPO release from PMN. Analysis of the binding of fluorescent C5a to PMN showed a direct correlation between decreased C5a binding and decreased O2- production and MPO release. Since all of these chemotactic factor-stimulated events are involved in the inflammatory process and the killing of microorganisms, alterations in these WBC functions in dialysis patients may contribute to their increased susceptibility to infection.

摘要

接受透析治疗的慢性肾衰竭患者更容易受到感染。以往研究表明,这些患者的体外中性粒细胞(PMN)趋化反应降低,PMN和单核细胞上的C5a受体可用性降低。本研究旨在确定血液透析(HD)和持续性非卧床腹膜透析(CAPD)患者的PMN和单核细胞的其他趋化因子介导反应是否异常。所研究的反应包括体外趋化性、超氧化物生成、H2O2产生和髓过氧化物酶(MPO)释放。这些研究表明,与正常对照组相比,HD和CAPD患者的PMN对C5a和fMLP的趋化反应显著降低。HD患者的PMN对C5a的反应平均降低了55.1%(p<0.005),CAPD患者降低了49.7%(p<0.01)。同样,HD患者对fMLP的趋化反应平均降低了44.7%(p<0.005),CAPD患者降低了36.3%(p<0.02)。与对照组相比,HD和CAPD患者的PMN和单核细胞对C5a和fMLP的刺激产生超氧阴离子的能力也显著降低。HD患者的PMN对C5a刺激产生超氧阴离子的能力平均降低了36.5%(p<0.001),CAPD患者降低了32.0%(p<0.001)。fMLP刺激产生的超氧阴离子也减少,但程度较小,HD患者平均减少18.0%(p<0.01),CAPD患者减少24.1%(p<0.01)。这种反应性降低仅限于C5a和fMLP刺激的超氧阴离子产生,因为佛波酯肉豆蔻酸酯乙酸酯(PMA)刺激的反应与对照组相当。在这些患者的单核细胞中也发现了类似的超氧阴离子产生减少模式。在PMN和单核细胞中H2O2产生的流式细胞术分析以及PMN中MPO释放的体外分析中,也观察到趋化因子刺激反应有类似程度的降低。对荧光C5a与PMN结合的分析表明,C5a结合减少与O2-产生和MPO释放减少之间存在直接相关性。由于所有这些趋化因子刺激的事件都参与炎症过程和微生物杀灭,透析患者这些白细胞功能的改变可能导致他们更容易受到感染。

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