Immunity is divided into innate immunity and adaptive immunity.
Innate immunity provides a first line of defense against pathogens without memory.
Adaptive immunity involves specific responses and has memory, allowing for a faster response during subsequent exposures.
Skin and mucous membranes act as physical barriers to prevent pathogen entry.
Chemical barriers include enzymes in saliva, tears, and other secretions that break down pathogens.
Cilia in the respiratory tract trap pathogens, helping to expel them before they enter the lungs.
Complement proteins: aid in the initial response to pathogens through opsonization and lysis.
Interferons: proteins released by infected cells that prevent the spread of pathogens to neighboring cells.
Natural Killer (NK) Cells: part of innate immunity that can also interact with cells involved in adaptive immunity (e.g., T cells).
Neutrophils: first responders that emerge from circulation to the site of tissue injury to combat infection, particularly against bacteria.
Macrophages and T lymphocytes: also involved in inflammation and pathogens capture.
Initiation: Triggered by tissue damage causing redness, heat, swelling, and pain.
Mobilization of Body Defenses: Increased blood flow (vasodilation) brings more immune cells to the site.
Clean Up and Repair: Monocytes migrate to clean up damaged tissue post-infection.
Types of T Cells:
Cytotoxic T Cells: kill infected or cancerous cells directly.
Helper T Cells: enhance the immune response by activating other immune cells.
Regulatory T Cells: moderate immune responses to prevent overactivity.
Memory T Cells: remain in circulation for faster response upon re-exposure to the same antigen.
Produce antibodies that target specific pathogens.
Different antibody classes (e.g., IgA, IgE) have specific functions in immune response.
Antigen Presentation: B cells can present antigens to T cells for more effective immune response activation.
Neutralization: Antibodies bind to pathogens to prevent their function.
Opsonization: Marking pathogens for destruction by phagocytes.
Agglutination: Clumping pathogens together to enhance phagocytosis.
Antigens are substances that trigger an immune response, identified by immune cells via Major Histocompatibility Complex (MHC).
Self-antigens: recognized as part of the body; foreign antigens trigger immune attacks.
Innate Immunity: Fast acting, non-specific, no memory, involves barriers and immediate cellular responses (e.g., phagocytes).
Adaptive Immunity: Slow to develop initially, specific to pathogens, has memory, involves T and B cells.
Injury and Pathogen Entry: Introduces bacteria to tissue; inflammation begins.
Vasodilation: Increases blood flow to the site to deliver immune cells.
Leukocyte Mobilization: Neutrophils and other leukocytes migrate through capillary gaps to reach the infection site.
Tissue Repair: Monocytes transition to macrophages to clean debris and regenerate tissue.