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Measuring the 50% Haemolytic Complement (CH50) Activity of Serum
Published on: March 29, 2010
Underlying complement deficiency in patients with disseminated gonococcal infection
R T Ellison1, J G Curd, P F Kohler
1Infectious Disease Section, Veterans Administration Medical Center, Denver, CO 80220.
Insights
Individuals with disseminated gonococcal infection often have complement deficiencies. This suggests that inherited or acquired complement issues are a key factor predisposing patients to Neisseria gonorrhoeae systemic infections.
Area of Science:
- Immunology
- Infectious Diseases
- Genetics
Background:
- The complement system is crucial for innate immunity.
- Disseminated gonococcal infection (DGI) is a severe manifestation of Neisseria gonorrhoeae infection.
- Complement deficiencies are known risk factors for Neisseria infections.
Purpose of the Study:
- To investigate the prevalence of complement system abnormalities in patients with DGI.
- To identify potential host factors predisposing individuals to DGI.
Main Methods:
- Serum complement activity was measured in 22 patients with DGI.
- Patients' complement levels were compared to normal population means.
- Specific complement component deficiencies (C1r, C4, C8) were assessed in affected individuals.
Main Results:
- Three out of 22 DGI patients (13.6%) had complement activity below normal.
- One patient had a complete C1r deficiency.
- Another patient had low C4 levels associated with systemic lupus erythematosus; a third had C8 deficiency.
Conclusions:
- The frequency of complement deficiencies is higher in DGI patients than in the general population.
- Inherited or acquired complement deficiencies are significant predisposing factors for DGI.
- Evaluating complement status may be important for managing patients at risk for DGI.
Abstract:
The complement system was evaluated in 22 individuals with disseminated gonococcal infection. Three of the 22 patients exhibited a total serum complement activity that was greater than 2 SD below the normal mean. Of these three, one had a complete deficiency of C1r, a second patient had pre-existing systemic lupus erythematosus with low levels of C4, and the third had a C8 concentration that was 60% of normal. We conclude that the prevalence of inherited or acquired complement deficiency among patients with disseminated gonococcal infection exceeds that among the general population and is an important host factor predisposing to systemic infection with Neisseria gonorrhoeae.
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