A high-throughput, bead-based, antigen-specific assay to assess the ability of antibodies to induce complement activation

被引:143
作者
Fischinger, Stephanie [1 ,2 ]
Fallon, Jonathan K. [1 ]
Michell, Ashlin R. [1 ]
Broge, Thomas [1 ]
Suscovich, Todd J. [1 ]
Streeck, Hendrik [2 ]
Alter, Galit [1 ]
机构
[1] Ragon Inst MGH Harvard & MIT, 400 Technol Sq, Cambridge, MA 02139 USA
[2] Univ Duisburg Essen, D-47057 Essen, Germany
关键词
ADCD; Complement; Antibody-dependent effector function; High-throughput; Fc receptor; GUINEA-PIG COMPLEMENT; FUNCTIONAL ANTIBODIES; 1ST COMPONENT; IN-VIVO; SYSTEM; SERUM; HIV; PROTECTION; EVOLUTION; RECEPTOR;
D O I
10.1016/j.jim.2019.07.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
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页数:12
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