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Questions and Answers
What is the primary function of C3b in the opsonization process?
What is the primary function of C3b in the opsonization process?
Which complement component is the most potent chemoattractant that attracts neutrophils to the site of infection?
Which complement component is the most potent chemoattractant that attracts neutrophils to the site of infection?
What occurs during class switching of B cells?
What occurs during class switching of B cells?
How does the binding of C3a, C4a, and C5a to mast cells contribute to inflammation?
How does the binding of C3a, C4a, and C5a to mast cells contribute to inflammation?
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What happens if excess immune complexes are not cleared from circulation?
What happens if excess immune complexes are not cleared from circulation?
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What is the main role of the membrane attack complex (MAC)?
What is the main role of the membrane attack complex (MAC)?
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Which pathway does not require antibodies for activation?
Which pathway does not require antibodies for activation?
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Which protein is involved in the lectin pathway that binds to mannose on the surface of pathogens?
Which protein is involved in the lectin pathway that binds to mannose on the surface of pathogens?
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Which of the following is a biological effect of complement activation?
Which of the following is a biological effect of complement activation?
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What components are unique to the classical pathway compared to the other pathways?
What components are unique to the classical pathway compared to the other pathways?
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What triggers the cleavage of MASP in the lectin pathway?
What triggers the cleavage of MASP in the lectin pathway?
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Which factor is needed for the activation of the alternative pathway?
Which factor is needed for the activation of the alternative pathway?
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Which component is not required for the lectin pathway to function?
Which component is not required for the lectin pathway to function?
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What is the primary function of complement proteins?
What is the primary function of complement proteins?
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What are the main proteins in the classical complement pathway?
What are the main proteins in the classical complement pathway?
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What is unique about IgM in relation to complement fixation?
What is unique about IgM in relation to complement fixation?
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How is complement inactivated?
How is complement inactivated?
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What distinguishes the larger and smaller fragments of complement proteins after activation?
What distinguishes the larger and smaller fragments of complement proteins after activation?
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Which of the following is NOT a characteristic of complement proteins?
Which of the following is NOT a characteristic of complement proteins?
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Which statement correctly describes the assembly of the complement pathway's C1 protein?
Which statement correctly describes the assembly of the complement pathway's C1 protein?
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Which ion is necessary for the activation of C1 subunits in the classic pathway?
Which ion is necessary for the activation of C1 subunits in the classic pathway?
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Which microbe-associated molecular pattern (MAMP) is specifically NOT found in the host?
Which microbe-associated molecular pattern (MAMP) is specifically NOT found in the host?
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What complex is formed by the cleavage of C4 and C2 in the classic pathway?
What complex is formed by the cleavage of C4 and C2 in the classic pathway?
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Which component stabilizes the C3 convertase in the alternative pathway?
Which component stabilizes the C3 convertase in the alternative pathway?
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What triggers the activation of the alternative pathway?
What triggers the activation of the alternative pathway?
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What is the primary role of C5b in the classic pathway?
What is the primary role of C5b in the classic pathway?
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Which of the following statements about C3b is correct?
Which of the following statements about C3b is correct?
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What best describes the function of C5a in the context of inflammation?
What best describes the function of C5a in the context of inflammation?
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Which factor cleaves B factor into Ba and Bb in the alternative pathway?
Which factor cleaves B factor into Ba and Bb in the alternative pathway?
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Study Notes
Complement System
- The complement system is a series of serum proteins that act as an enzyme cascade, produced by the liver.
- It's present in all body fluids except cerebrospinal fluid (CSF) and urine.
- It exists in an inactive form, becoming active upon activation, then leading to lysis of antigens (Ag).
- The complement system has more than 23 proteins, ranging from C1 to C9.
- A high concentration of complement proteins is found in guinea pig serum, making it suitable for in vitro experiments related to complement activation.
- Complement proteins are thermolabile, meaning they are inactivated at 56°C for 30 minutes or even fewer hours at room temperature.
- Complement proteins are designated by capital letter C followed by Arabic numbers (e.g., C1, C2).
- Each protein, after activation, has two subunits (a and b).
- The smaller fragment is designated 'a'.
- The larger fragment is designated 'b', except for C2a, which is larger than C2b.
- Larger fragments bind to functional complexes while smaller fragments diffuse into the circulatory system.
Complement Pathways
- Complement activation occurs through three pathways: the classical pathway, the lectin pathway, and the alternative pathway.
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Classical pathway: Triggered by antigen-antibody complexes (IgM and IgG).
- C1 binds to the Fc portion of the antibody.
- C1 activates C1r and C1s (esterase activity).
- C1s cleaves C4 and C2.
- C4b and C2a form C3 convertase (C4b2a).
- C3 convertase cleaves C3 into C3a and C3b.
- C3b joins C4b2a to form C5 convertase (C4b2a3b).
- C5 convertase cleaves C5 into C5a and C5b.
- C5b initiates the formation of the membrane attack complex (MAC).
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Alternative pathway: Activated by microbial components like lipopolysaccharide (LPS) and endotoxins, and is part of the innate immune system.
- No antibody (Ab) is required.
- C3 undergoes spontaneous hydrolysis to form C3(H2O).
- Factor B binds to C3(H2O).
- Factor D cleaves Factor B into Ba and Bb.
- C3b, Bb, and properdin (factor P) form C3 convertase (C3bBb).
- C3 convertase further cleaves C3 and forms C5 convertase (C3bBb3b) which cleaves C5 into C5a and C5b.
- C5b initiates the formation of the MAC.
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Lectin pathway: Activated by mannose-binding lectin (MBL) binding to mannose residues on microbial surfaces.
- MBL binds to pathogen surfaces.
- MBL-associated serine proteases (MASPs) cleave C4 and C2.
- This forms the C3 convertase, similar to the classical pathway.
Complement Activity Regulation
- Complement activation is tightly regulated by proteins.
- Proteins on cell surfaces, such as sialic acid, facilitate the inactivation of complement components.
- Control proteins such as CD59, inhibits MAC formation.
- Serum proteins like C1 inhibitor, Factor H, and Factor I regulate complement activation.
Consequences of Complement Activation
- Lysis of pathogens: MAC formation causes lysis of cells by forming pores in their membranes.
- Opsonization: C3b and C4b enhance phagocytosis by binding to pathogens.
- Inflammation: C3a, C4a, and C5a act as chemoattractants, attracting neutrophils.
- Neutralization of viruses and toxins: C3b contributes to this process.
- Clearance of immune complexes: Immune complexes are removed from the circulation.
- Enhancement of antibody production: C3b binds to complement receptors on B cells leading to B cell proliferation and class switching.
Complement Deficiencies
- Deficiencies in complement components can lead to recurrent infections, immune complex diseases, and other issues.
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Description
Test your knowledge on the complement system, including the functions of various complement components and their roles in opsonization, inflammation, and B cell class switching. This quiz covers key processes and pathways within the immune response.