Ragon Institute of MGH, Harvard and MIT, Cambridge 02139, USA; University of Duisburg-Essen, Essen 47057, Germany.
Ragon Institute of MGH, Harvard and MIT, Cambridge 02139, USA.
J Immunol Methods. 2019 Oct;473:112630. doi: 10.1016/j.jim.2019.07.002. Epub 2019 Jul 10.
The complement system plays a critical role in innate immune defense against pathogens, both via non-specific direct pathogen recognition and killing or via antigen-specific indirect recruitment by complement fixing antibodies. While various assays for measuring complement activation have been developed, few provide a high-throughput, sample-sparing approach to interrogate the qualitative differences in the ability of antibodies to drive complement activation. Here we present a high-throughput, sample-sparing, bead-based assay to evaluate antigen-specific antibody-dependent complement activation against nearly any antigen. Optimization of buffer composition, kinetics of immune complex formation, as well as complement source all contribute critically to the development of a robust, highly flexible and high-throughput approach to analyze antibody-dependent complement deposition (ADCD). Thus, the optimized bead-based, antigen-specific assay represents a simple, highly adaptable platform to profile antibody-dependent complement activation across pathogens and diseases.
补体系统在先天免疫防御病原体中起着关键作用,既可以通过非特异性直接识别和杀伤病原体,也可以通过补体固定抗体的抗原特异性间接募集。虽然已经开发了各种用于测量补体激活的测定方法,但很少有方法提供高通量、节省样本的方法来探究抗体驱动补体激活能力的定性差异。在这里,我们提出了一种高通量、节省样本的基于珠子的测定方法,用于评估针对几乎任何抗原的抗原特异性抗体依赖性补体激活。缓冲液组成的优化、免疫复合物形成的动力学以及补体来源都对开发一种稳健、高度灵活和高通量的方法来分析抗体依赖性补体沉积(ADCD)至关重要。因此,优化后的基于珠子的、抗原特异性测定方法代表了一种简单、高度适应的平台,可以在病原体和疾病之间分析抗体依赖性补体激活。