Key Points of Immune Responses
Types of Immune Responses
Two main types:
Humoral Immunity (B lymphocytes, antibodies)
Cell-Mediated Immunity (CMI) (T lymphocytes)
B Lymphocytes and Humoral Immunity
B cells produce antibodies; specifically, plasma cells secrete antibodies.
Antibodies mark antigens for destruction, but do not destroy directly.
Differentiation based on antigen location:
Extracellular antigens: Activate humoral immunity.
Intracellular antigens: Activate CMI.
Antibodies
Types of Immunoglobulins:
Immunoglobulin M (IgM)
Characteristic | Description |
|---|---|
Structure | Pentamer when secreted (10 antigen-binding sites); monomer on B cell surface. |
Location | Found in blood and lymph; also on the surface of B cells. |
Abundance | ~5-10% of total serum immunoglobulins; first antibody produced in a primary immune response. |
Function | Potent agglutinator, highly effective in activating the complement system, marks extracellular pathogens for destruction. |
Immunoglobulin G (IgG)
Characteristic | Description |
|---|---|
Structure | Monomer (2 antigen-binding sites). |
Location | Most abundant Ig in serum (~80% of total serum Ig); found in blood, lymph, and intestines; capable of crossing the placenta to provide passive immunity to the fetus. |
Abundance | ~80% of total serum immunoglobulins; main antibody of secondary immune response. |
Function | Neutralizes toxins and viruses, enhances phagocytosis (opsonization), triggers ADCC, and activates the complement system. |
Immunoglobulin A (IgA)
Characteristic | Description |
|---|---|
Structure | Dimer in secretions (4 antigen-binding sites, held by a J chain and secretory component); monomer in serum. |
Location | Predominant Ig in secretions (mucus, tears, saliva, breast milk, gastrointestinal and genitourinary tracts) where it protects mucous membrane surfaces; also found in blood and lymph (~10-15% of total serum Ig). |
Abundance | ~10-15% of total serum immunoglobulins. |
Function | Prevents microbial attachment to mucous membranes, neutralizes toxins and viruses locally, provides local immunity. |
Immunoglobulin D (IgD)
Characteristic | Description |
|---|---|
Structure | Monomer (2 antigen-binding sites). |
Location | Primarily found on the surface of naive B cells, acting as a B cell receptor; very low concentration in serum (<0.2% of total serum Ig). |
Abundance | Less than 0.2% of total serum immunoglobulins. |
Function | Acts as an antigen receptor on B cells, signaling B cell activation. |
Immunoglobulin E (IgE)
Characteristic | Description |
|---|---|
Structure | Monomer (2 antigen-binding sites). |
Location | Primarily found bound to mast cells and basophils in tissues; very low concentration in serum (least abundant serum Ig). |
Abundance | Least abundant Ig in serum. |
Function | Mediates allergic reactions (e.g., binds to mast cells and basophils, triggering histamine release upon antigen binding) and plays a crucial role in defense against parasitic worms. |
Antibody functions in immune response (general overview):
Agglutination: Clumping of antigens, facilitating phagocytosis.
Opsonization: Coating antigens to enhance phagocytosis.
Neutralization: Blocking pathogen attachment and action.
ADCC (Antibody-Dependent Cell-Mediated Cytotoxicity): Targets parasitic worms and virally infected cells, activating effector cells like eosinophils, NK cells, and macrophages.
T Lymphocytes and Cell-Mediated Immunity (CMI)
T cells mature in the thymus; five types:
Helper T cells (Th): Activate other immune cells.
Cytotoxic T cells (Tc): Destroy infected cells on contact.
Regulatory T cells (Tr): Suppress immune response to prevent autoimmunity.
Delayed Type T cells (Td): Cause delayed reactions such as hypersensitivity.
Memory T cells: Provide quicker response upon re-exposure to antigens.
CMI targets intracellular pathogens by recognizing processed antigens on cell surfaces.
Antigen Presentation
APCs (Antigen Presenting Cells): Include dendritic cells and macrophages, present processed antigens to T helper cells.
Immunological Memory
Primary Response: Initial response to antigen, slower, produces memory B cells and IgM first, then IgG.
Secondary Response: Faster due to memory B cells; produces IgG first, higher antibody levels than primary response.
Summary of Function
Vaccinations stimulate primary immune response, creating memory for faster future responses.
Continuous review of immune processes is necessary for retention of knowledge.