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Updated: Aug 17, 2026

Measuring the 50% Haemolytic Complement (CH50) Activity of Serum
Published on: March 29, 2010
Complement and its breakdown products in SLE
1Department of Rheumatology, University Hospital of Lund, SE-22185 Lund, Sweden. Gunnar.Sturfelt@reum.lu.se
Insights
The complement system protects the body but can harm tissues if overactivated. Understanding this dual role is key for treating infections and autoimmune diseases like SLE.
Area of Science:
- Immunology
- Complement System Biology
Background:
- The complement system is crucial for innate and adaptive immunity.
- Inappropriate complement activation can lead to tissue damage and autoimmune diseases, such as Systemic Lupus Erythematosus (SLE).
- Complement deficiency increases susceptibility to infections and autoimmune conditions.
Purpose of the Study:
- To review the dual role of the complement system in health and disease.
- To discuss complement activation pathways, products, and their involvement in autoimmunity.
- To explore the therapeutic potential of complement regulation.
Main Methods:
- Literature review of complement system functions and dysregulation.
- Analysis of complement's role in immune responses and pathogenesis.
- Discussion of current understanding and future therapeutic strategies.
Main Results:
- The complement system exhibits protective functions and pathogenic potential.
- Complement activation pathways and products are detailed.
- Autoimmunity against complement components and their therapeutic targeting are examined.
Conclusions:
- The complement system's dual role necessitates careful therapeutic modulation.
- Understanding complement regulation offers promising avenues for treating immune-related disorders.
- Targeting the complement system holds potential for novel therapeutic interventions.
Abstract:
The complement system has important protective functions in both the innate and the adaptive immune systems but can also, when inappropriately activated, cause tissue damage. Complement deficiency predisposes to infection and also to development of autoimmune disease, especially SLE, and complement is at the same time involved in the pathogenesis of this disease. In this review, various aspects of this dualism are discussed. An overview of activation pathways and activation products is given, together with a description of autoimmunity against complement and the potential of complement regulation in future therapeutics.
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