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Updated: Aug 10, 2026

Isolation of Labile Multi-protein Complexes by in vivo Controlled Cellular Cross-Linking and Immuno-magnetic Affinity Chromatography
Published on: March 10, 2010
[Determination of circulating immune complexes by immunoenzyme method]
Insights
A new enzyme immunoassay accurately measures circulating immune complexes (CIC) in human blood serum. This method, using Staphylococcus aureus protein, shows good correlation with existing techniques for detecting CICs.
Area of Science:
- Immunology
- Biochemistry
- Clinical Chemistry
Background:
- Circulating immune complexes (CIC) are implicated in various diseases.
- Accurate measurement of CICs is crucial for diagnosis and monitoring.
- Existing methods for CIC detection have limitations.
Purpose of the Study:
- To develop and validate a novel enzyme immunoassay (EIA) for quantifying CICs in human serum.
- To assess the efficacy of the EIA in detecting CICs formed by different immunoglobulin classes.
- To compare the performance of the proposed EIA with established methods.
Main Methods:
- Enzyme immunoassay (EIA) utilizing Staphylococcus aureus protein for plate sensitization.
- Optimization of S. aureus protein concentration for optimal plate sensitization (1-5 µg/ml).
- Comparative analysis of EIA results with established methods (Haskova et al., Digeon et al.).
Main Results:
- The developed EIA effectively measures CICs in human blood serum.
- The method is capable of detecting CICs involving various immunoglobulin classes.
- Results obtained by the proposed EIA demonstrated good correlation with two other established methods.
Conclusions:
- The proposed enzyme immunoassay provides a reliable and accurate method for measuring circulating immune complexes.
- This EIA offers a valuable tool for clinical diagnostics and research involving CICs.
- The method's ability to detect different immunoglobulin classes enhances its utility.
Abstract:
Enzyme immunoassay is proposed to be used for measuring the content of circulating immune complexes (CIC) in human blood serum. S. aureus protein in a concentration of 1 to 5 micrograms/ml optimal for the sensitization of plates is used as the first sandwich layer. The method permits registration of CICs formed by immunoglobulins of different classes. Investigations of the blood sera of donors and cancer patients by the proposed method and by other methods (V. Haskova et al. and M. Digeon et al.) to assess complex formation showed a good correlation of the results of all measurements.
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