Adaptive Defenses: Specialized responses that recognize specific antigens.
Specific: Targets specific antigens (example: flu virus).
Systemic: Responses are not limited to the site of initial infection.
Memory: Strengthened responses upon re-exposure to known antigens.
Humoral Immunity: Mediated by antibodies in the blood.
Involves B cells producing antibodies that bind to pathogens.
Cellular Immunity: Involves T cells.
Directly kills infected cells or marks them for destruction.
Involves a respiratory burst, generating reactive oxygen species.
Marks target cells for destruction by phagocytes.
Antigens: Substances that provoke immune responses.
Targets adaptive immunity; usually large, complex, and nonself molecules.
Antigenic Determinants: Unique parts of antigens that trigger immune responses.
Natural antigens can activate multiple lymphocyte populations.
Large, simple molecules have low immunogenicity.
Almost any protein is recognized by antibodies.
Antibody regions include recognition sites for specific antigens.
Normal immunoglobulin levels:
High IgM, IgG; low IgE.
Allergic Reactions: High levels of IgE associated with allergies.
Sequence from B cell activation to plasma cells producing IgE leading to allergic responses.
MHC Role: Essential for T cell education and immune function.
Presents foreign proteins on cell surfaces to be recognized by T cells.
Mutations can cause T cells to attack the body’s cells.
MHC Proteins: Self-antigens crucial for distinguishing self from nonself.
Unique to the individual, important for organ transplant compatibility.
B Lymphocytes (B Cells): Humoral immunity, produce antibodies upon activation.
T Lymphocytes (T Cells): Cell-mediated immunity.
Antigen Presenting Cells (APCs):
Essential for presenting antigens to T cells.
Include dendritic cells and macrophages.
T Cell Education: Occurs in the thymus; involves negative and positive selection.
Positive selection ensures T cells recognize self-MHC.
Negative selection eliminates self-reactive T cells.
Naive B and T cells are immunocompetent but not yet exposed to antigens.
Once exposed, they undergo clonal selection and activation.
Clonal Selection: Naive lymphocyte's first antigen encounter results in activation.
Proliferation and Differentiation: Activated lymphocytes become effector cells or memory cells.
Memory cells circulate to respond more quickly upon re-exposure.
APCs engulf antigens and present fragments to T cells for recognition.
Major types include dendritic cells, macrophages, and B cells.
Differentiation into CD4+ (helper) and CD8+ (cytotoxic) T cells.
Helper T cells activate B cells, T cells, and macrophages.
Cytotoxic T cells kill infected cells, foreign cells, and tumor cells.
Requires APC presentation and assistance from helper T cells.
Cytotoxic Mechanisms:
Release of perforins to create pores in target cell membranes.
Induction of apoptosis in infected or abnormal cells.
Vaccines activate adaptive immune responses and create memory T and B cells.
Can contain dead, living, or engineered viruses for immune stimulation.
Example: Cowpox utilized by Edward Jenner for smallpox vaccination.
High incidence of severe cases each year, requires annual vaccine updates based on viral mutations.
mRNA technology used to induce immune response and memory formation.
Concerns regarding adjuvants enhancing immune responsiveness.