Innate Immunity
INNATE IMMUNITY OVERVIEW
1. Definition
Susceptibility: Lack of resistance to a disease.
Immunity: Ability to ward off disease.
Innate Immunity: Defenses against any pathogen that does not require prior exposure.
Adaptive Immunity: Immunity or resistance to a specific pathogen.
2. Lines of Defense
2.1 First Line of Defense
Physical Barriers:
Intact skin
Mucous membranes and their secretions.
Normal microbiota (compete with pathogens).
Physical Factors:
Mucus: Traps microbes.
Ciliary Escalator: Moves trapped microbes away from lungs.
Lacrimal Apparatus: Washes eyes.
Saliva: Washes microbes off mouth.
Urine & Vaginal Secretions: Flows out, helping to eliminate microbes.
Chemical Factors:
Seba: Contains fungistatic fatty acids.
Skin pH: Low pH (3-5) inhibits bacterial growth.
Lysozyme: Found in perspiration, tears, saliva, and urine; breaks down bacterial cell walls.
Gastric Juice pH: Very low (1.2-3.0), kills microbes.
2.2 Second Line of Defense
Phagocytic Cells:
Neutrophils, macrophages, eosinophils: Engulf and digest pathogens.
Inflammation:
Response to tissue damage, characterized by red, swollen, painful areas.
Fever: Abnormally high body temperature enhances immune response.
Antimicrobial Substances:
Complement proteins and interferons enhance the immune response.
3. Cell Types in Immunity
3.1 Leukocytes (White Blood Cells)
Types of Leukocytes: 5000-10,000 per ul or mm³
Granulocytes:
Neutrophils (60-70%): Phagocytosis.
Eosinophils (2-4%): Combat parasitic infections and some phagocytosis.
Basophils (0.5-1%): Involved in inflammatory responses (release histamine).
Agranulocytes:
Monocytes (3-8%): Differentiate into macrophages and dendritic cells to perform phagocytosis.
Lymphocytes (20-25%): Natural killer (NK) cells destroy infected or cancerous cells; T cells and B cells participate in adaptive immunity.
4. Phagocytosis Process
Steps:
Chemotaxis and adherence of phagocyte to microbe.
Ingestion of microbe via pseudopods forming a phagosome.
Fusion of phagosome with lysosome, forming a phagolysosome.
Digestion of ingested microbes by lysosomal enzymes.
Formation of residual body with indigestible material.
Discharge of waste products.
5. Inflammation Process
Components:
Activation of acute-phase proteins (complement, cytokines).
Blood vessel changes (vasodilation, increased permeability from histamine and kinin).
Symptoms: Redness, swelling, pain, heat.
Phagocyte recruitment (margination and diapedesis).
6. Fever
Mechanism:
Caused by release of interleukin-1 (IL-1) from phagocytes responding to pathogens.
Hypothalamus adjusts body temperature set-point.
Benefits: Enhances immune activity and inhibits pathogen growth.
Risks: High fever can lead to serious complications (e.g., tachycardia, dehydration).
7. Complement System
Function:
Series of serum proteins activated in a cascade.
Three pathways: Classical, Alternative, and Lectin.
Outcomes: Opsonization (enhanced phagocytosis), inflammation, cell lysis (MAC).
8. Interferons
Role:
IFN-alpha and IFN-beta: Induce antiviral protein production in neighboring cells.
IFN-gamma: Enhances phagocytosis by neutrophils and macrophages.