Six Mechanisms of Innate Defense:
Species Resistance:
Certain species are naturally resistant to diseases affecting other species.
Environmental factors of the body can prevent pathogen survival.
Mechanical Barriers:
Considered the "First line of Defense."
Includes skin and mucus membranes which keep pathogens out.
Bodily fluids like sweat and mucus help rinse away pathogens.
Chemical Barriers:
Body fluids contain enzymes that digest pathogens.
Examples: Stomach acid and tear enzymes.
Interferon:
Peptides responding to viruses and tumor cells, blocking virus replication and stimulating phagocytosis.
Fever:
Elevated body temperature restricts iron availability from the liver and spleen, hindering bacterial and fungal survival.
Increases the activity of phagocytic cells.
Inflammation:
Provides a localized response to tissue damage and pathogen presence.
Phagocytosis:
Specialized cells that engulf and digest pathogens.
Specific Defenses:
Provides resistance to specific pathogens or toxins (specific types of immunity).
Immunity:
Developed through exposure, allowing lymphocytes and macrophages to "remember" pathogens for future protection.
Antigens:
Recognition molecules, typically proteins or sugars, utilized by the immune system to distinguish self from non-self substances.
Red Bone Marrow:
Releases stem cells for lymphopoiesis (the formation of lymphocytes).
Half of these stem cells migrate to the thymus to become T Cells.
The other half remain in bone marrow to mature into B Cells.
Circulation:
T cells circulate in the blood looking for antigens ("trouble").
Activation Process:
Antigen Presenting Cells (APC), such as macrophages and B cells, present foreign antigens to T cells to activate them.
Macrophage Activity:
Macrophages consume pathogens and present antigens combined with Major Histocompatibility Complex (MHC) molecules to T cells to activate an immune response.
Types of T Cells:
T-Helper (CD4):
Activates B cells.
T-Cytotoxic (CD8):
Recognizes foreign antigens on infected or cancerous cells and kills them.
T-Memory Cells:
Persist after an infection, allowing faster responses if the same pathogen reappears.
Development:
B cells mature in bone marrow, with some circulating while others reside in immune organs.
Humoral Immune Response:
B cells combat pathogens by releasing antibodies through plasma cells.
Antibodies, also known as Immunoglobulins (Ig), play a crucial role in identifying and neutralizing pathogens.
IgG:
Predominant in plasma and tissues, crosses the placenta, and combats bacteria, viruses, and toxins.
IgM:
Present in blood, examples include Anti-A and Anti-B, involved in the response against bacterial antigens.
IgA:
Found in mucosal areas (e.g., breast milk, tears, gastric juice); acts as a first line of defense in secretions.
IgD:
Located on B cell surfaces, particularly in children, important for B cell activation.
IgE:
Associated with allergic reactions, binds to mast cells to trigger responses upon allergen contact.
Direct Attack:
Antibodies bind to antigens to neutralize them or cause clumping for easier phagocytosis.
Complement Activation:
Binding of IgG and IgM activates complement proteins, which can opsonize pathogens, attract phagocytic cells, and cause cell membrane lysis.
Primary Immune Response:
First encounter with a pathogen, slow antibody production lasts weeks.
Secondary Immune Response:
Re-exposure leads to quicker antibody production due to memory cells, providing faster protection.
Natural vs. Artificial:
Natural immunity occurs through everyday exposure, whereas artificial immunity is obtained through intentional exposure like vaccines.
Active vs. Passive:
Active immunity is generated when the body produces antibodies, providing long-lasting protection.
Passive immunity involves receiving antibodies from another source, offering temporary protection.
Examples:
Natural, active immunity could arise from a pneumonia infection; natural, passive from breastfeeding; artificial, active from vaccinations; artificial, passive from antivenoms or antitoxins.