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Updated: Nov 9, 2025

Methods for Quantitative Detection of Antibody-induced Complement Activation on Red Blood Cells
Published on: January 29, 2014
Detection of Complement Factor B Autoantibodies by ELISA.
Mihály Józsi1, Barbara Uzonyi2
1Department of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary. mihaly.jozsi@gmx.net.
Autoantibodies targeting factor B can stabilize complement enzymes, potentially causing kidney disease. This study introduces an ELISA to detect these specific autoantibodies.
Area of Science:
- Immunology
- Complement System Biology
- Autoimmunity
Background:
- Autoantibodies are linked to numerous diseases, often by triggering pathological complement activation.
- Autoantibodies targeting complement proteins are particularly implicated in kidney diseases.
- Antibodies binding to complement convertases can enhance their stability and resistance to regulation, promoting complement turnover.
Purpose of the Study:
- To describe a novel ELISA method for detecting autoantibodies against factor B.
- To investigate if these autoantibodies bind to and stabilize the alternative complement pathway C3 convertase enzyme, C3bBb.
Main Methods:
- Development and application of an enzyme-linked immunosorbent assay (ELISA).
- Detection of autoantibodies targeting factor B.
- Assessment of antibody binding to and stabilization of the C3bBb complex.
Main Results:
- The study successfully developed an ELISA method to detect factor B autoantibodies.
- These autoantibodies were found to bind to the C3 convertase enzyme C3bBb.
- The binding of autoantibodies contributed to the stabilization of the C3bBb complex.
Conclusions:
- Factor B autoantibodies can bind to and stabilize the alternative pathway's C3 convertase, C3bBb.
- This stabilization may contribute to abnormal complement activation.
- The developed ELISA is a valuable tool for identifying factor B autoantibodies in diseases like kidney disease.
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