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Updated: Aug 23, 2025

Measuring the 50% Haemolytic Complement CH50 Activity of Serum
Published on: March 29, 2010
Pitfalls in complement analysis: A systematic literature review of assessing complement activation
Ricardo J M G E Brandwijk1, Marloes A H M Michels2, Mara van Rossum1
1R&D Department, Hycult Biotechnology b.v., Uden, Netherlands.
Insights
Accurate complement analysis is crucial for disease monitoring, but many studies fail to use proper sample handling and assay techniques. Standardized guidelines are needed to ensure reliable complement biomarker measurements.
Area of Science:
- Immunology
- Clinical Chemistry
Background:
- The complement system is a key part of innate immunity and involved in numerous diseases.
- Accurate assessment of complement activation is vital for disease monitoring and treatment evaluation.
- Standardized sampling and assay procedures for complement analysis are challenging to implement.
Conclusions:
- A significant portion of studies deviate from standardized procedures for complement analysis.
- Improper sample handling and techniques can lead to misinterpretation of complement biomarker levels.
- There is a critical need for general guidelines to ensure accurate and standardized complement analysis.
Background:
The complement system is an essential component of our innate defense and plays a vital role in the pathogenesis of many diseases. Assessment of complement activation is critical in monitoring both disease progression and response to therapy. Complement analysis requires accurate and standardized sampling and assay procedures, which has proven to be challenging.
Objective:
We performed a systematic analysis of the current methods used to assess complement components and reviewed whether the identified studies performed their complement measurements according to the recommended practice regarding pre-analytical sample handling and assay technique. Results are supplemented with own data regarding the assessment of key complement biomarkers to illustrate the importance of accurate sampling and measuring of complement components.
Methods:
A literature search using the Pubmed/MEDLINE database was performed focusing on studies measuring the key complement components C3, C5 and/or their split products and/or the soluble variant of the terminal C5b-9 complement complex (sTCC) in human blood samples that were published between February 2017 and February 2022. The identified studies were reviewed whether they had used the correct sample type and techniques for their analyses.
Results:
A total of 92 out of 376 studies were selected for full-text analysis. Forty-five studies (49%) were identified as using the correct sample type and techniques for their complement analyses, while 25 studies (27%) did not use the correct sample type or technique. For 22 studies (24%), it was not specified which sample type was used.
Conclusion:
A substantial part of the reviewed studies did not use the appropriate sample type for assessing complement activation or did not mention which sample type was used. This deviation from the standardized procedure can lead to misinterpretation of complement biomarker levels and hampers proper comparison of complement measurements between studies. Therefore, this study underlines the necessity of general guidelines for accurate and standardized complement analysis.
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