Related Experiment Video
Updated: May 1, 2026

Depletion of Specific Cell Populations by Complement Depletion
Published on: February 5, 2010
The complement system: history, pathways, cascade and inhibitors
Insights
The complement system, discovered in the 19th century, is clinically significant in various conditions like autoimmune diseases and transplant injury. This review covers its history, activation pathways, and regulators.
Area of Science:
- Immunology
- Biochemistry
Background:
- The complement system is a critical part of the innate immune system.
- It plays a role in host defense, inflammation, and clearance of immune complexes.
- Dysregulation is linked to numerous diseases.
Purpose of the Study:
- To provide a historical overview of the complement system's discovery and evolution.
- To summarize the key activation pathways of the complement cascade.
- To discuss the regulatory mechanisms that control complement activity.
Main Methods:
- Literature review of historical and contemporary research on the complement system.
- Synthesis of information on complement activation pathways (classical, lectin, alternative).
- Analysis of known complement regulatory proteins and their functions.
Main Results:
- The complement system has a rich history dating back to the 19th century.
- Three main pathways converge to activate the complement cascade.
- A complex network of regulators prevents self-damage.
Conclusions:
- The complement system is a vital and complex immunological entity.
- Understanding its pathways and regulation is crucial for clinical applications.
- Further research continues to uncover its multifaceted roles in health and disease.
Abstract:
Since its discovery in the 19th century, the complement system has developed into a clinically significant entity. The complement system has been implicated in a variety of clinical conditions, from autoimmune diseases to ischemia-reperfusion injury in transplantation. This article charts the historical progress of our understanding of the complement system and provides a synopsis on the activation pathways and its inherent regulators.
More Related Videos
06:54Evaluation of the Interplay Between the Complement Protein C1q and Hyaluronic Acid in Promoting Cell Adhesion
Published on: June 15, 2019
07:26High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
Published on: July 18, 2017
Related Concept Videos
Complement System
Antimicrobial Proteins
Interferons
Interferons (IFNs) are proteins produced by lymphocytes, macrophages, and fibroblasts infected with viruses. While IFNs cannot prevent viruses from entering and...
Defense Against Bacterial Pathogens
Phagocytes
Phagocytes are the frontline soldiers of the immune system. They include neutrophils and macrophages. Neutrophils are the most abundant type of white blood cell and are quickly mobilized to the site of infection. Macrophages are larger cells that patrol...
Antibody Actions
Neutralization
Antibodies can bind to pathogens, preventing them from infecting host cells. This process...
Hypersensitivity Reactions: Cytolytic Reactions
Extrinsic and Intrinsic Pathways of Hemostasis
The Extrinsic Pathway
The extrinsic pathway of coagulation is typically initiated by tissue damage that exposes blood to tissue factor (TF), a protein released by the damaged tissue cells outside the blood vessels—this interaction with TF triggers biochemical reactions involving specific clotting factors. The key player here is Factor VII, which...