Seelen M A, Roos A, Wieslander J, Mollnes T E, Sjöholm A G, Wurzner R, Loos M, Tedesco F, Sim R B, Garred P, Alexopoulos E, Turner M W, Daha M R
Department of Nephrology, C3P-29, Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.
J Immunol Methods. 2005 Jan;296(1-2):187-98. doi: 10.1016/j.jim.2004.11.016. Epub 2004 Dec 15.
Primary defence against invading microorganisms depends on a functional innate immune system and the complement system plays a major role in such immunity. Deficiencies in one of the components of the complement system can cause severe and recurrent infections, systemic diseases, such as systemic lupus erythematosus (SLE) and renal disease. Screening for complement deficiencies in the classical or alternative complement pathways has mainly been performed by haemolytic assays. Here, we describe a simple ELISA-based format for the evaluation of three pathways of complement activation. The assays are based on specific coatings for each pathway in combination with specific buffer systems. We have standardized these assays and defined cut off values to detect complement deficiencies at the different levels of the complement system. The results demonstrate the value of these ELISA-based procedures for the functional assessment of complement deficiencies in clinical practice. The assay is now available commercially in kit form.
抵御入侵微生物的主要防线依赖于功能正常的固有免疫系统,补体系统在这种免疫中发挥着主要作用。补体系统的某一成分缺乏可导致严重且反复的感染、系统性疾病,如系统性红斑狼疮(SLE)和肾脏疾病。经典或替代补体途径中补体缺陷的筛查主要通过溶血试验进行。在此,我们描述了一种基于酶联免疫吸附测定(ELISA)的简单方法,用于评估补体激活的三条途径。这些试验基于每条途径的特异性包被以及特定的缓冲系统。我们已对这些试验进行了标准化,并确定了临界值,以检测补体系统不同水平的补体缺陷。结果证明了这些基于ELISA的方法在临床实践中对补体缺陷进行功能评估的价值。该试验现在已有商用试剂盒形式。