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Understanding the Humoral Immune Response
Jan 20, 2025
Humoral Immune Response
Overview
Initiated when B cells encounter a target antigen.
Leads to production of antibodies specific to the antigen.
Antibodies help mark antigens for destruction.
Activation of B Cells
B cells activated when antigen binds to receptor on surface.
Binding causes cross-linking and receptor-mediated endocytosis (clonal selection).
B cells proliferate and differentiate into effector cells.
Role of T Cells
Interactions with T cells often required for full activation of B cells.
Plasma Cells
Most clone cells become plasma cells.
Plasma cells secrete specific antibodies (up to 2,000/sec) for 4-5 days.
Memory Cells
Clone cells that do not become plasma cells become memory cells.
Memory cells enable a rapid response to future exposures to the same antigen.
Primary vs. Secondary Immune Response
Primary Response:
Lag period of 3-6 days after antigen encounter.
Peak plasma cell production at 10 days, then declines.
Secondary Response:
Faster and more effective due to memory cells.
Peak antibody levels within 2-3 days.
Higher antibody levels than primary response.
Active Humoral Immunity
Naturally Acquired:
Formed in response to actual infection.
Artificially Acquired:
Formed in response to vaccination.
Passive Humoral Immunity
Naturally Acquired:
Antibodies delivered via placenta or breast milk.
Artificially Acquired:
Injection of antibodies (e.g., gamma globulin).
Used in rapidly fatal diseases.
Antibodies (Immunoglobulins)
Structure
T or Y-shaped monomers with 4 polypeptide chains.
Composed of 2 heavy and 2 light chains.
Variable region: antigen binding site.
Constant region: determines antibody class.
Classes of Antibodies
IgM:
First released, potent agglutinating agent.
Pentamer structure.
IgA:
Found in mucous and secretions.
Prevents pathogen entry.
IgD:
Acts as a receptor on B cell surface.
IgG:
Most abundant, secondary and late primary responses.
Crosses placental barrier.
IgE:
Involved in allergies and parasitic infections.
Antibody Function
Do not destroy antigens but mark them for destruction.
Mechanisms include neutralization, agglutination, precipitation, and complement fixation.
Monoclonal Antibodies
Production and Use
Commercially prepared, specific to single antigenic determinant.
Produced by hybridomas (tumor cell and B cell fusion).
Used in clinical and research applications.
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