调理大肠杆菌K-12诱导人中性粒细胞化学发光的定量评价

Thomas W. Jungi , Anton Schmid , Andreas Morell , Peter J. Spaeth , Ernst Peterhans
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引用次数: 2

摘要

利用鲁米诺增强的化学发光(CL)作为PMN刺激的参数,定量了活化的大肠杆菌K-12细菌与多形核白细胞(PMN)的相互作用。在双对数尺度上,光发射取决于预调理期间使用的调理素浓度。最有效的cl诱导剂是新鲜人血清,其刺激活性依赖于完整的补体(C)系统。通过加热或用EGTD阻断经典C途径使C失活,可使cl诱导效力降低8 - 16倍。低γ球蛋白热血清介导的小CL。静脉注射IgG介导CL的生成,但还原/烷基化和硫酸溶解降低了刺激能力。有证据表明,用于替代的商业IgG和IgM中的抗k -12抗体不能提高IgG缺乏,IgM和c充足的血清的刺激能力,除非替代非常高的Ig浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative assessment of human neutrophil chemiluminescence induced by opsonized Escherichia coli K-12

The interaction of opsonized E. coli K-12 bacteria and polymorphonuclear leukocytes (PMN) was quantified, using luminol-enhanced chemiluminescence (CL) as a parameter of PMN stimulation. On a double-logarithmic scale light emission depended on the opsonin concentration used during pre-opsonisation. The most potent CL-inducing agent was fresh human serum, and its stimulatory activity depended on an intact complement (C) system. Both inactivation of C by heating or blocking the classical C pathway with EGTD decreased the CL-inducing potency by a factor of 8 to 16. Hypogammaglobulinemic heated serum mediated little CL. IgG for intravenous use mediated CL generation, but reduction/alkylation and sulphitolysis reduced the stimulatory power. Evidence is presented that the anti-K-12 antibodies within commercial IgG and IgM used for substitution do not improve the stimulatory power of IgG-deficient, IgM- and C-sufficient serum, unless very high Ig concentrations are substituted.

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