CHAPTER 21- PEARSON NOTES
Overview of the Immune System
Every second, hostile bacteria, fungi, and viruses challenge our health.
Healthy body despite constant exposure due to the immune system's efficiency.
The immune system is functional rather than anatomical, involving diverse molecules and trillions of immune cells (especially lymphocytes).
Comparison to medieval castle defenses—three lines of defense.
Three Lines of Defense
Surface Barriers
First line of defense is intact skin and mucosae.
Functions as structural barriers (similar to castle walls and moats).
Coated in secretions (e.g., mucus, tears).
Innate Internal Defenses
Second line of defense activated when surface barriers are penetrated.
Utilizes internal defenses such as:
Antimicrobial proteins.
Phagocytes (cells that engulf pathogens).
Other immune cells.
Characteristics:
Always present, checks for friend or foe, capable of direct attack and calling reinforcements.
Hallmark: inflammation.
Adaptive (Specific) Defense System
Third line of defense functions like elite soldiers with specialized weapons.
Slower to respond to invaders, must be trained (specific immunity).
Adaptive and innate immunity are interconnected; both release and recognize similar molecules, communicate, and assist each other in immune responses.
Effective against microorganisms, cancer cells, and transplants, providing both direct attacks and mobilizing chemicals for broader responses.
Part 1: Innate Defenses
Innate defenses include mechanical barriers, cells, and chemicals ready from birth.
Critical for reducing the workload of the adaptive system by preventing entry and spread of pathogens.
1.1 Surface Barriers
Skin and mucous membranes provide first line of defense with keratin as a physical barrier.
Characteristics of surface membranes:
Acidic secretions: inhibit bacterial growth.
Enzymes: Lysozyme destroys bacteria; protein-digesting enzymes kill microorganisms in the stomach.
Mucin: forms sticky mucus, trapping microorganisms.
Defensins: antimicrobial peptides secreted to help control microbial colonization.
Other chemicals: lipid components of sebum and dermcidin in sweat are toxic.
Key Elements of Surface Membranes:
Intact epidermis.
Mucosal linings (digestive, respiratory, urinary, reproductive).
1.2 Innate Internal Defenses
Internal innate defenses consist of cells and chemicals as second line of defense, including:
Phagocytes: the primary types are neutrophils (abundant, first responders) and macrophages (voracious eaters).
Natural Killer (NK) cells: destroy virus-infected and cancer cells without needing specific antigens. They induce apoptosis in targets.
Inflammation: A vital process that includes:
Preventing spread of damaging agents.
Disposing of debris and pathogens.
Alerting adaptive immune response.
Setting stage for repair.
Inflammatory Response Characteristics:
Four cardinal signs:
Redness
Heat
Swelling
Pain
Possible fifth sign: impaired function.
Phagocytosis:
Mechanism:
Adhesion: Phagocyte adheres to pathogen.
Engulfment: Membrane surrounds and engulfs pathogen, forming phagosome.
Lysosome fusion: Phagosome fuses with lysosome to form phagolysosome.
Destruction: Digestive enzymes break down external material.
Exocytosis: Expelling indigestible material.
Opsonization:
Pathogen “tasty” through opsonins (complements or antibodies) allowing easier phagocytosis.
Phagocyte Mobilization During Inflammation:
Leukocytosis: Increase in white blood cells (neutrophils).
Margination: Phagocytes adhere to blood vessel walls.
Diapedesis: Phagocytes squeeze through capillary walls to reach site.
Chemotaxis: Migration towards chemical signals released by damaged cells or pathogens.
Neutrophils & Monocytes Role:
Neutrophils act quickly as first responders.
Monocytes become macrophages, enhancing phagocytosis and tissue repair.
Additional Innate Defenses:
Antimicrobial Proteins
Interferons: Secreted by infected cells to warn nearby cells.
Complement System: Helps lyse pathogens and enhances phagocytosis by opsonization.
Part 2: Adaptive Defenses
Adaptive immunity is delayed and requires exploits against specific pathogens or foreign substances (antigens). It provides long-term protection through memory cells.
2.1 Immobilization of Antigen via Antigens
Antigen: Molecules that B and T lymphocytes recognize and respond to.
Complete Antigen: Has both immunogenicity and reactivity.
Hapten: Incomplete antigen that only becomes immunogenic when linked to a body protein.
Antigenic Determinants: Portion of an antigen recognized by lymphocytes.
2.2 Lymphocyte Classes
Two major classes: B lymphocytes (humoral immunity) and T lymphocytes (cell-mediated immunity).
Lymphocytes rely on antigen recognition for activation and proliferation.
Summary of Lymphocytes:
B cells produce antibodies and differentiate into memory cells & plasma cells.
T cells differentiate into helper T cells, cytotoxic T cells, and regulatory T cells.
2.3 Antigen-Presenting Cells:
APCs include dendritic cells, macrophages, and B cells that help activate T cells by presenting processed antigens.
Dendritic cells: Key role in antigen capture and presentation, linking innate and adaptive immunity.
Key Points on Vaccination and Immunity:
Active Immunity: Developed from exposure to pathogens.
Passive Immunity: Temporary immunity from anti-serum or maternal antibodies.
Homeostatic Imbalance:
Lack of immune response can lead to diseases like HIV/AIDS, wherein the immune system fails to protect against infection due to lack of T cells.
Autoimmune Disorders:
Conditions wherein the immune system attacks own tissues (e.g., rheumatoid arthritis).
Hypersensitivity Reactions:
Delayed and immediate hypersensitivities leading to allergic reactions or autoimmune responses.
Summary of Immunity Development:
The immune system matures through exposure to antigens and can weaken with age, leading to increased susceptibility to infections and immune disorders.