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What is the difference between active and passive immunity?
Active = body produces its own immune response; Passive = immunity borrowed (e.g., antibodies from another source).
What are the types of immunity based on how they are acquired?
Natural (through infection or maternal antibodies) and Artificial (via vaccination or antibody injection).
How long does it typically take adaptive immunity to respond fully?
Around 28 days.
What type of white blood cells are central to adaptive immunity?
Lymphocytes (B cells and T cells).
Where do B cells and T cells originate and mature?
Originate: Bone marrow; Mature: B cells – bone marrow, T cells – thymus.
What is an antigen?
A foreign substance that triggers an immune response; often a protein or polysaccharide.
What is an epitope?
The specific part of an antigen that binds to a receptor on B or T cells.
What is an antibody (immunoglobulin)?
A protein produced by B cells that binds to specific antigens.
How diverse are B and T cell receptors?
Over 1 million B-cell types; over 10 million T-cell types.
What does self-tolerance mean?
The immune system can distinguish self from non-self to avoid attacking the body’s own cells.
What is immunological memory?
The ability of the immune system to respond more quickly to pathogens it has encountered before.
What is the difference between a primary and secondary immune response?
Primary: slower (10–17 days); Secondary: faster (2–7 days), stronger, more efficient.
What happens during clonal selection?
Activated B/T cells divide into effector cells (to fight) and memory cells (for future response).
What shape are B-cell receptors and what do they bind?
Y-shaped; bind directly to free antigens.
What do B cells produce upon activation?
Antibodies (immunoglobulins).
What kind of pathogens do B cells respond to?
Extracellular pathogens (e.g., in blood or lymph).
Do T cells produce antibodies?
No, they recognize antigen fragments and directly kill infected cells or help other cells.
compare and contrast key terms
Term | Definition | Compare With | Key Differences |
---|---|---|---|
Antigen | A foreign molecule that triggers an immune response | Epitope | Epitope is a specific part of an antigen |
Antibody (Ig) | Protein made by B cells that binds to antigens | Antigen | Antibody is made in response to antigen |
Epitope | Specific region on an antigen recognized by receptors | Antigen | Epitope is the part that binds to immune receptors |
Passive Immunity | Borrowed antibodies (e.g., injection or maternal) | Active Immunity | Passive is temporary and externally sourced |
Natural Immunity | Acquired via infection or maternal antibodies | Artificial Immunity | Artificial immunity is induced by vaccines |
Compare and Contrast Characteristics of Adaptive Immunity
Characteristic | Adaptive Immunity | Innate Immunity | Difference |
---|---|---|---|
Specificity | Highly specific to antigens | General, broad pattern recognition | Adaptive targets specific invaders |
Memory | Long-term memory present | No memory | Adaptive “remembers” previous infections |
Response Time | Slow (days) | Fast (minutes–hours) | Innate is immediate; adaptive takes longer |
Diversity | Millions of receptors | Limited receptor types | Adaptive recognizes more pathogens |
Self-Tolerance | Yes | Partially | Adaptive trained to avoid attacking self |
Compare and Contrast B and T Cells
Feature | B Cells | T Cells |
---|---|---|
Maturation Site | Bone marrow | Thymus |
Target | Pathogens in fluids | Infected cells |
Receptor Shape | Y-shaped | Linear receptor |
Antigen Recognition | Direct binding | Needs antigen presentation (MHC) |
Secretes | Antibodies | Cytokines or cytotoxic proteins |
Main Subtypes | Plasma cells, Memory B cells | Helper T cells, Cytotoxic T cells |
Sequence B and T Cell Function
B Cell Function:
Detects and binds to antigen in fluid
Activates (with or without T cell help)
Clonal expansion
Differentiates into plasma and memory B cells
Plasma cells produce antibodies
T Cell Function:
APC presents antigen on MHC
T cell binds to antigen-MHC complex
Helper T cells activate via cytokines
Cytotoxic T cells destroy infected cells
Both generate memory T cells
Hypothesize and Diagnose the Impact of Variability on B & T Cells
Scenario | Possible Outcome |
---|---|
Low receptor diversity | Fewer pathogens recognized → poor immune coverage |
Loss of self-tolerance | Autoimmune response → attacks own body |
Failure of clonal expansion | Weak immune response → insufficient effector cells |
No memory cell formation | Re-infection leads to full response again → no fast recovery |
Compare and Contrast Responses to Antigens
Feature | Cell-Mediated Response | Humoral Response |
---|---|---|
Involved Cells | Cytotoxic T cells | B cells and antibodies |
Target | Infected cells | Pathogens in blood/fluids |
Trigger | Antigen presented on MHC I | Antigen binds to B cell receptor |
Mechanism | Perforin and granzymes kill cells | Antibodies neutralize and opsonize |
End Result | Infected cells destroyed | Pathogens neutralized or phagocytosed |
Sequence Responses to Antigens
Pathogen enters body
APC engulfs and presents antigen
Helper T cell binds to presented antigen
Helper T cell secretes cytokines
Cytokines activate B cells and cytotoxic T cells
B cells produce antibodies
Cytotoxic T cells kill infected cells
Memory cells are created
Hypothesize and Diagnose the Impact of Variability on Responses to Antigens
Change or Defect | Predicted Impact |
---|---|
APC fails to present antigen | No T cell activation → entire adaptive response compromised |
No cytokine production by Helper T cells | No activation of B cells or cytotoxic T cells |
Mutation in antigen structure | Immune evasion → no recognition by immune cells |
Failure to produce antibodies | Poor humoral response → extracellular pathogens persist |
Sequence Vaccine Activity
Vaccine (antigen or genetic material) is introduced into the body
APCs take up the material and present the antigen
Helper T cells recognize and bind to the presented antigen
Helper T cells release cytokines
Cytokines activate B cells and cytotoxic T cells
B cells produce antibodies; cytotoxic T cells prepare for response
Memory B and T cells form
Future exposures trigger rapid secondary response