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尿毒症患者B淋巴细胞功能的体外分析

In vitro analysis of B lymphocyte function in uraemia.

作者信息

Degiannis D, Mowat A M, Galloway E, Tsakiris D, Briggs J D, Junor B J, Parrott D M

机构信息

Department of Bacteriology and Immunology, Western Infirmary, Glasgow, UK.

出版信息

Clin Exp Immunol. 1987 Nov;70(2):463-70.

Abstract

We have investigated the immune responses in vitro of uraemic patients undergoing regular haemodialysis or continuous ambulatory peritoneal dialysis. Twenty-five healthy subjects were also studied as controls. In uraemic patients, the number of T and B lymphocytes were within the normal range, but proliferative responses to phytohaemagglutinin (PHA) were impaired. Spontaneous immunoglobulin plaque forming cell (PFC) responses by peripheral blood mononuclear cells (PBMC) from uraemic patients were significantly lower than those of healthy subjects. The PFC response of uraemic PBMC to the T cell independent polyclonal B cell activator (PBA) Epstein-Barr virus (EBV) was comparable to the response of the healthy subjects, indicating that uraemic B cells are still capable of synthesizing immunoglobulin. Pokeweed mitogen (PWM) induced PFC responses of uraemic PBMC were also normal, whereas the response to another T cell dependent B cell activator, Staphylococcus aureus Cowan I (SAC), was very low. Addition of indomethacin to PWM- and SAC-activated cultures of uraemic PBMC enhanced the PFC response to SAC, but had little effect on the PWM response. As full differentiation of B cells in response to SAC depends on helper T cells, we conclude that a defect in T lymphocyte function accounts for the reduced spontaneous and SAC induced production of immunoglobulin by uraemic PBMC. This defect may be mediated by an indomethacin-sensitive mechanism.

摘要

我们研究了接受定期血液透析或持续性非卧床腹膜透析的尿毒症患者的体外免疫反应。还研究了25名健康受试者作为对照。在尿毒症患者中,T淋巴细胞和B淋巴细胞的数量在正常范围内,但对植物血凝素(PHA)的增殖反应受损。尿毒症患者外周血单个核细胞(PBMC)的自发免疫球蛋白空斑形成细胞(PFC)反应明显低于健康受试者。尿毒症PBMC对T细胞非依赖性多克隆B细胞激活剂(PBA)爱泼斯坦-巴尔病毒(EBV)的PFC反应与健康受试者的反应相当,表明尿毒症B细胞仍有合成免疫球蛋白的能力。美洲商陆有丝分裂原(PWM)诱导的尿毒症PBMC的PFC反应也正常,而对另一种T细胞依赖性B细胞激活剂金黄色葡萄球菌Cowan I(SAC)的反应非常低。在尿毒症PBMC的PWM和SAC激活培养物中添加吲哚美辛可增强对SAC的PFC反应,但对PWM反应影响不大。由于B细胞对SAC的完全分化依赖于辅助性T细胞,我们得出结论,T淋巴细胞功能缺陷导致尿毒症PBMC自发和SAC诱导的免疫球蛋白产生减少。这种缺陷可能由一种对吲哚美辛敏感的机制介导。

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