首页> 美国卫生研究院文献>Annals of the Rheumatic Diseases >Effects of coagulation temperature on measurements of complement function in serum samples from patients with systemic lupus erythematosus.
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Effects of coagulation temperature on measurements of complement function in serum samples from patients with systemic lupus erythematosus.

机译:凝血温度对系统性红斑狼疮患者血清样品补体功能测定的影响。

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摘要

Blood samples from 15 patients with systemic lupus erythematosus (SLE) and 15 healthy blood donors were allowed to coagulate for one hour at room temperature, followed by one hour at 4 or 37 degrees C. The complement activity of the serum samples was assessed by three different functional assays. Serum samples from patients with SLE obtained by coagulation at 37 degrees C had a lower complement activity than serum samples from blood coagulated at 4 degrees C when the capacity of the serum samples to solubilise precipitable immune complexes and to support the attachment of complement factors to solid phase immune complexes was determined. Haemolytic complement activity was not affected by the coagulation temperature. The content of C1q binding immune complexes in paired serum samples obtained after coagulation at 4 and 37 degrees C was similar and the size distribution of the immune complexes, determined by high performance gel permeation chromatography, was also similar. This study shows that the results of functional complement assays, applied to serum samples from patients with SLE cannot be compared unless the conditions for blood coagulation and serum handling are defined and are the same. The data also indicate that assays measuring complement mediated solubilisation of immune complexes and the fixation of complement factors to solid phase immune complexes are more sensitive indicators of complement activity than the haemolytic assay.
机译:将15位系统性红斑狼疮(SLE)患者和15位健康献血者的血液样品在室温下凝固1小时,然后在4或37摄氏度下凝固1小时。通过3次评估血清样品的补体活性不同的功能测定。当血清样品能溶解可沉淀的免疫复合物并支持补体因子与固体的结合时,在37℃下凝结的SLE患者的血清样品的补体活性低于在4℃下凝结的血液的血清样品的补体活性。确定了免疫相。溶血补体活性不受凝结温度的影响。在4和37℃下凝固后获得的配对血清样品中与C1q结合的免疫复合物的含量相似,并且通过高效凝胶渗透色谱法测定的免疫复合物的大小分布也相似。这项研究表明,除非确定了凝血和血清处理的条件并且相同,否则无法比较应用于SLE患者血清样品的功能性补体测定的结果。数据还表明,与溶血测定法相比,测量补体介导的免疫复合物增溶和补体因子固定于固相免疫复合物的测定法是补体活性的更敏感指标。

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