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血液中S100A12(EN-RAGE)的定量因采样方法、钙和肝素而异。

Quantification of S100A12 (EN-RAGE) in blood varies with sampling method, calcium and heparin.

作者信息

Larsen A, Bronstein I B, Dahl O, Wentzel-Larsen T, Kristoffersen E K, Fagerhol M K

机构信息

Section of Oncology, Institute of Internal Medicine, University of Bergen, Bergen, Norway.

出版信息

Scand J Immunol. 2007 Feb;65(2):192-201. doi: 10.1111/j.1365-3083.2006.01875.x.

Abstract

S100A12 is a calcium-binding protein predominantly found in neutrophil granulocytes and monocytes. Its usefulness in monitoring inflammatory disease states depends on documentation that assay results are reliable. This study aimed at defining guidelines for blood sampling, selection of optimal material handling and reference intervals in healthy controls while taking into account the basic features of S100A12. An enzyme linked immunosorbent assay was developed based upon antibodies induced in rabbits by injection of recombinant S100A12. Our studies confirm that oligomers of S100A12 are generated in the presence of calcium. Structural changes in S100A12 mediated by calcium influence the interaction with antibody. This is proposed as the background for our very low readings of S100A12 in Ethylene Diamine Tetraacetic Acid (EDTA) plasma. Individual S100A12 levels did not change substantially over a 5-week sampling period. Based upon testing of 150 blood donors we suggest reference intervals of S100A12 in serum to be 49-1340 microg/l for women and 27-1750 microg/l for men. The estimated mean concentrations were 234 microg/l in serum samples (range 12-15791), 114 microg/l (range 3-17282) in re-calcified EDTA plasma and 48 microg/l (range 2-14843) in heparin plasma. Without adding calcium to EDTA plasma before running the assay, concentrations were around 2 microg/l (16 persons). S100A12 quantification is assumed to become relevant for diagnostic use in many disease states. The importance of the handling and analysing conditions for a reliable result was examined. We recommend serum collected in gel-containing tubes as the preferred sample material and have suggested reference intervals for healthy individuals.

摘要

S100A12是一种主要存在于中性粒细胞和单核细胞中的钙结合蛋白。其在监测炎症疾病状态方面的实用性取决于检测结果可靠的文献记录。本研究旨在确定血液采样、最佳材料处理选择以及健康对照者参考区间的指南,同时考虑S100A12的基本特征。基于注射重组S100A12诱导兔产生的抗体,开发了一种酶联免疫吸附测定法。我们的研究证实,S100A12的寡聚体在钙存在的情况下生成。钙介导的S100A12结构变化影响其与抗体的相互作用。这被认为是我们在乙二胺四乙酸(EDTA)血浆中S100A12读数极低的背景原因。在为期5周的采样期内,个体S100A12水平并无显著变化。基于对150名献血者的检测,我们建议血清中S100A12的参考区间为女性49 - 1340微克/升,男性27 - 1750微克/升。血清样本的估计平均浓度为234微克/升(范围12 - 15791),重新钙化的EDTA血浆中为114微克/升(范围3 - 17282),肝素血浆中为48微克/升(范围2 - 14843)。在检测前未向EDTA血浆中添加钙时,浓度约为2微克/升(16人)。S100A12定量被认为在许多疾病状态的诊断应用中具有相关性。研究了获得可靠结果的处理和分析条件的重要性。我们推荐使用含凝胶管收集的血清作为首选样本材料,并给出了健康个体的参考区间。

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