Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Complement System01:27

Complement System

The complement system is a group of approximately 20 plasma proteins that strengthen the body's defenses against infections through opsonization, inflammation, and cell lysis. Opsonization involves coating pathogens with complement proteins, making them more recognizable and facilitating phagocyte engulfment. Certain complement proteins induce inflammation that attracts immune cells to the site of infection. Cell lysis involves the destruction of pathogens through the formation of a membrane...
Antibody Actions01:26

Antibody Actions

Antibodies, or immunoglobulins, are critical players in the immune system's arsenal against invading pathogens. Produced by B cells and plasma cells, their primary role is to detect and bind to specific antigens, molecules found on the surface of pathogens like bacteria or viruses. Beyond antigen recognition, antibodies perform several vital functions that contribute to immune defense.
Neutralization
Antibodies can bind to pathogens, preventing them from infecting host cells. This process...
Antimicrobial Proteins01:23

Antimicrobial Proteins

Antimicrobial proteins are important components of the immune system. They aid the body in combating pathogens by either killing them directly or hindering their replication processes. Four main types of antimicrobial substances are interferons, the complement system, iron-binding proteins, and antimicrobial proteins.
Interferons
Interferons (IFNs) are proteins produced by lymphocytes, macrophages, and fibroblasts infected with viruses. While IFNs cannot prevent viruses from entering and...
Humoral Immune Responses01:36

Humoral Immune Responses

Overview
Hypersensitivity Reactions: Immune-Complex Reactions01:19

Hypersensitivity Reactions: Immune-Complex Reactions

Type III hypersensitivity reactions occur when antigen–antibody complexes form and activate the complement system. Normally, these complexes help the clearance of antigens by phagocytes and red blood cells. However, when large numbers of immune complexes are present, they can deposit in tissues—particularly in the walls of blood vessels—leading to inflammation and tissue injury. These deposits trigger complement activation and neutrophil recruitment, resulting in serum sickness, a systemic...
Defense Against Bacterial Pathogens01:31

Defense Against Bacterial Pathogens

The human immune system is a complex network of cells, tissues, and organs that work together to defend the body against bacterial infections. It consists of various immune cells, each playing a specific role in the defense mechanism.
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...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The immunochemistry of toxins and toxoids; the solubility and precipitation of tetanal toxin and toxoid in methanol-water mixtures under controlled conditions of pH, ionic strength and temperature.

Journal of immunology (Baltimore, Md. : 1950)·2010
Same author

The immunochemistry of toxins and toxoids; the preparation and immunologic evaluation of purified tetanol toxoid.

Journal of immunology (Baltimore, Md. : 1950)·2010
Same author

The isolation and crystallization of tetanal toxin.

Science (New York, N.Y.)·2010
Same author

A Preliminary Study of the Chemical Nature of the Toxic Substances produced by the Salmonella Group of Organisms.

The Journal of hygiene·2010
Same author

Chemical studies on blood and muscle from rabbits and rats paralyzed by dithiobiuret.

Federation proceedings·2010
Same author

The action of crystalline tetanal toxin in white Swiss mice.

Federation proceedings·2010

Related Experiment Video

Updated: Jun 19, 2026

Methods for Quantitative Detection of Antibody-induced Complement Activation on Red Blood Cells
06:29

Methods for Quantitative Detection of Antibody-induced Complement Activation on Red Blood Cells

Published on: January 29, 2014

THE ROLE OF THE COMPONENTS OF COMPLEMENT IN SPECIFIC IMMUNE FIXATION.

L Pillemer1, S Seifter, E E Ecker

  • 1Institute of Pathology, Western Reserve University, and the University Hospitals, Cleveland.

The Journal of Experimental Medicine
|October 30, 2009
PubMed
Summary
This summary is machine-generated.

Complement fixation involves multiple components, with C'4 and C'2 binding to immune aggregates. This study clarifies the roles of complement components (C'1, C'2, C'3, C'4) in immune reactions.

More Related Videos

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
07:26

High-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

Depletion of Specific Cell Populations by Complement Depletion
06:17

Depletion of Specific Cell Populations by Complement Depletion

Published on: February 5, 2010

Related Experiment Videos

Last Updated: Jun 19, 2026

Methods for Quantitative Detection of Antibody-induced Complement Activation on Red Blood Cells
06:29

Methods for Quantitative Detection of Antibody-induced Complement Activation on Red Blood Cells

Published on: January 29, 2014

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
07:26

High-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

Depletion of Specific Cell Populations by Complement Depletion
06:17

Depletion of Specific Cell Populations by Complement Depletion

Published on: February 5, 2010

Area of Science:

  • Immunology
  • Biochemistry

Background:

  • The complement system is crucial for immune responses.
  • Understanding complement component fixation to immune aggregates is vital for elucidating immune mechanisms.

Purpose of the Study:

  • To investigate the fixation patterns of individual complement components to specific immune aggregates.
  • To determine the factors influencing complement component binding and inactivation.

Main Methods:

  • Experiments involving antigen-antibody aggregates and varying concentrations of complement components.
  • Analysis of complement component inactivation and adsorption under different experimental conditions (temperature, pH, time).

Main Results:

  • C'4 is invariably inactivated/adsorbed by specific aggregates, indicating it's a combining component.
  • C'2 is fixed with C'4, while C'3 fixation is partial or absent.
  • Mid-piece (containing C'1) shows variable adsorption.
  • Thermolabile serum constituents are necessary for C'4 fixation.
  • Specific immune fixation involves C'4, C'2, and C'1, differing from non-specific adsorption.

Conclusions:

  • Complement fixation is a complex process involving multiple components, primarily C'4-C'2 and C'1, binding to antigen-antibody complexes.
  • C'4 is directly involved in specific immune fixation, with its binding influenced by thermolabile factors.
  • The findings challenge the notion of mid-piece (C'1) as the sole combining complement component.