Chapter 11: Immunity in Humans
Understand the body's defense mechanisms against pathogens, from physical barriers to specific immune responses and vaccination strategies.
Chapter 11: Immunity in Humans
Learning Objectives
By the end of this chapter, you should be able to:
- Describe the three lines of defense in the human immune system
- Explain specific and non-specific immune responses
- Understand the roles of different white blood cells
- Compare active and passive immunity
- Analyze vaccination principles and their importance
Overview
The human immune system is a complex network of defenses that protects the body from harmful pathogens, foreign substances, and abnormal cells. It operates through multiple layers of protection, from physical barriers to highly specific immune responses. Understanding immunity is crucial for comprehending how the body fights infections, prevents diseases, and maintains overall health.
Body's Defense System
Three Lines of Defense
The immune system is organized into three overlapping lines of defense that provide comprehensive protection against pathogens.
First Line of Defense: Physical and Chemical Barriers
Non-specific defense that prevents pathogens from entering the body
Physical Barriers:
| Barrier | Description | Mechanism of Protection |
|---|---|---|
| Skin | Intact skin with keratin layer | Prevents pathogen entry; waterproof |
| Mucous Membranes | Linings of respiratory, digestive, urinary tracts | Traps pathogens; contains antimicrobial substances |
| Cilia | Hair-like structures in respiratory tract | Moves mucus and trapped particles upward |
| Tears | Fluid secreted by lacrimal glands | Washes eyes; contains lysozyme enzyme |
| Saliva | Fluid secreted by salivary glands | Washes mouth; contains lysozyme and antibodies |
| Mucus | Slimy secretion in respiratory and digestive tracts | Traps pathogens; contains antimicrobial substances |
Chemical Barriers:
| Chemical Defense | Source | Mechanism |
|---|---|---|
| Lysozyme | Tears, saliva, mucus | Degrades bacterial cell walls |
| Stomach Acid | Gastric glands | Low pH kills most pathogens |
| Defensins | Various tissues | Antimicrobial peptides |
| Interferons | Infected cells | Signal neighboring cells to defend against viruses |
Importance:
- Prevents most pathogen entry
- Non-specific - works against various pathogens
- Constant protection without prior exposure
Did You Know? The skin is the body's largest organ and sheds about 30,000-40,000 dead skin cells every minute, creating a physical barrier that is constantly renewed to prevent pathogen entry!
Barrier Efficiency Equation:
Second Line of Defense: Internal Cellular and Chemical Defenses
Non-specific defense that activates when pathogens breach first line
Inflammatory Response:
Process:
- Tissue Damage: Pathogens or injury damage tissues
- Chemical Release: Damaged cells release histamine and other chemicals
- Blood Vessel Changes: Vasodilation increases blood flow
- Plasma Leakage: Increased permeability allows white blood cells to exit vessels
- Phagocytosis: White blood cells engulf and digest pathogens
Signs of Inflammation:
- Redness (Rubor): Increased blood flow
- Heat (Calor): Increased blood temperature
- Swelling (Tumor): Fluid leakage into tissues
- Pain (Dolor): Pressure on nerve endings
- Loss of Function (Functio Laesa): Impaired tissue function
Phagocytic Cells:
| Cell Type | Source | Function | Efficiency |
|---|---|---|---|
| Neutrophils | Bone marrow | Rapid response, bacterial phagocytosis | High for bacteria |
| Macrophages | Various tissues | Antigen presentation, phagocytosis | Broad spectrum |
| Dendritic Cells | Tissues | Antigen presentation to lymphocytes | Specialized for presentation |
| Monocytes | Blood | Differentiate into macrophages/dendritic cells | Precursor cells |
Phagocytosis Efficiency Equation:
Fever Response:
- Trigger: Pyrogens (fever-inducing substances) from pathogens
- Mechanism: Hypothalamus raises body temperature set point
- Benefits:
- Inhibits pathogen growth
- Enhances immune cell activity
- Improves antibody production
Natural Killer (NK) Cells:
- Function: Destroy virus-infected and cancerous cells
- Mechanism: Detect abnormal cells and induce apoptosis
- Importance: Early defense against viral infections and cancer
Third Line of Defense: Specific Immune Response
Highly specific defense involving lymphocytes and memory cells
Lymphocytes: The main cells of specific immunity
- T Lymphocytes (T cells): Cell-mediated immunity
- B Lymphocytes (B cells): Humoral immunity
- Origin: Bone marrow, mature in thymus (T cells) and bone marrow (B cells)
Antigen Recognition:
- Antigens: Foreign molecules that trigger immune response
- Epitopes: Specific parts of antigens recognized by antibodies/T cells
- Antibodies: Y-shaped proteins produced by B cells
- Receptors: Specific receptors on lymphocytes recognize antigens
Specific Immune Responses:
| Response Type | Main Cells | Target | Mechanism |
|---|---|---|---|
| Cell-mediated | T cells | Infected cells, cancer cells | Direct destruction of abnormal cells |
| Humoral | B cells, antibodies | Extracellular pathogens | Antibody-mediated neutralization |
T Lymphocytes (T Cells)
Types and Functions:
| T Cell Type | Function | Target Cells |
|---|---|---|
| Helper T cells (CD4+) | Coordinate immune response, activate other immune cells | Present antigens via MHC II |
| Cytotoxic T cells (CD8+) | Directly destroy infected and cancerous cells | Present antigens via MHC I |
| Regulatory T cells (Tregs) | Suppress immune response, prevent autoimmunity | Self-antigens, activated immune cells |
| Memory T cells | Provide long-term immunity | Previously encountered antigens |
T Cell Activation Process:
- Antigen Presentation: Antigen-presenting cells display antigens
- Co-stimulation: Helper T cells provide activation signals
- Proliferation: Clonal expansion of specific T cells
- Differentiation: T cells become effector or memory cells
- Effector Functions: Destruction of target cells or immune coordination
B Lymphocytes (B Cells)
Functions:
- Antibody Production: Create specific antibodies against antigens
- Antigen Presentation: Similar to macrophages
- Memory Cell Formation: Create long-lasting immunity
Antibody Structure:
- Y-shaped protein with two identical heavy chains and two identical light chains
- Variable regions: Bind to specific antigens
- Constant regions: Determine antibody class and function
Antibody-Antigen Binding Equation:
Antibody Specificity:
Antibody Classes (Immunoglobulins):
| Class | Structure | Location | Function |
|---|---|---|---|
| IgG** | Monomer | Blood, tissues | Main antibody in blood; crosses placenta |
| IgM | Pentamer | Blood | First antibody produced; complement activation |
| IgA | Dimer | Mucous secretions | Mucosal immunity; prevents pathogen attachment |
| IgD | Monomer | B cell surface | B cell receptor |
| IgE** | Monomer | Basophils, mast cells | Parasite defense; allergic reactions |
Antibody Functions:
- Neutralization: Block pathogen attachment/invasion
- Opsonization: Mark pathogens for phagocytosis
- Complement Activation: Trigger inflammatory response
- Agglutination: Clump pathogens together for easier removal
Antibody-Pathogen Interaction:
Types of Immunity
Active Immunity
Definition: Body produces its own antibodies in response to antigen exposure
Characteristics:
- Long-lasting: Provides years or lifetime protection
- Delayed onset: Takes time to develop (1-2 weeks)
- Memory cells: Creates immunological memory
Natural Active Immunity
- Source: Natural infection with pathogen
- Examples: Recovering from chickenpox, measles
- Advantages: Strong, long-lasting protection
- Disadvantages: Risk of disease complications
Artificial Active Immunity
- Source: Vaccination with weakened/attenuated pathogens
- Examples: Measles vaccine, polio vaccine, COVID-19 vaccine
- Mechanism: Simulates infection without disease
- Benefits: Safe, confers immunity, reduces disease spread
Passive Immunity
Definition: Receive antibodies from external source
Characteristics:
- Immediate protection: No waiting period
- Short-term: Lasts weeks to months
- No memory cells: No immunological memory
Natural Passive Immunity
- Source: Transfer from mother to fetus/infant
- Mechanisms:
- Placenta: IgG antibodies cross placenta during pregnancy
- Breast milk: IgA antibodies provided through breastfeeding
- Benefits: Protects newborns before their immune system matures
Artificial Passive Immunity
- Source: Injection of pre-formed antibodies
- Examples:
- Antiserum: Antibodies against specific toxins (snake venom, tetanus)
- Immune Globulin: pooled antibodies for specific diseases
- Uses: Post-exposure prophylaxis, treatment for certain infections
- Duration: Temporary protection (weeks to months)
Comparison of Immunity Types
| Feature | Active Natural | Active Artificial | Passive Natural | Passive Artificial |
|---|---|---|---|---|
| Source | Natural infection | Vaccination | Mother to child | Antibody injection |
| Speed | Slow (1-2 weeks) | Slow (1-2 weeks) | Immediate | Immediate |
| Duration | Long (years/lifetime) | Long (years) | Short (months) | Short (weeks/months) |
| Memory Cells | Yes | Yes | No | No |
| Risk | Disease risk | Minimal risk | No risk | No risk |
| Examples | Chickenpox recovery | MMR vaccine | Maternal antibodies | Antivenom, tetanus shot |
Vaccination and Immunization
Principles of Vaccination
Herd Immunity: When enough people are vaccinated, pathogens cannot spread effectively, protecting even unvaccinated individuals
Types of Vaccines:
| Vaccine Type | Description | Examples | Advantages |
|---|---|---|---|
| Live Attenuated | Weakened but live pathogens | MMR, chickenpox | Strong, long-lasting immunity |
| Inactivated | Killed pathogens | IPV, flu shot | Safe for immunocompromised |
| Subunit/Recombinant | Specific antigens only | Hepatitis B, HPV | Minimal side effects |
| Toxoid | Inactivated toxins | Tetanus, diphtheria | Safe, effective |
| mRNA | Genetic code for antigen | COVID-19 | Rapid development, highly effective |
Vaccination Schedule:
- Infancy: Multiple vaccines for preventable diseases
- Childhood: Boosters and additional vaccines
- Adolescence: Tdap, HPV, meningococcal vaccines
- Adulthood: Annual flu shots, tetanus boosters, travel vaccines
Vaccine Development and Testing
Clinical Trials Process:
- Preclinical Testing: Laboratory and animal studies
- Phase I: Small human trials (20-100 people)
- Phase II: Larger human trials (100-1000 people)
- Phase III: Large-scale trials (thousands of people)
- Phase IV: Post-marketing surveillance
Safety and Efficacy:
- Safety: Monitor for adverse reactions
- Efficacy: Measure effectiveness in preventing disease
- Regulatory Approval: Agencies like FDA, EMA evaluate data
Vaccine Efficacy Calculation:
Herd Immunity Threshold:
where = basic reproduction number
Immune Disorders
Hypersensitivity Reactions
Overactive immune responses to harmless substances
| Type | Mechanism | Examples | Treatment |
|---|---|---|---|
| Type I (Immediate) | IgE-mediated, rapid | Allergies (food, pollen), asthma | Antihistamines, epinephrine |
| Type II (Cytotoxic) | Antibody-mediated cell destruction | Transplant rejection, autoimmune hemolytic anemia | Immunosuppressants |
| Type III (Immune Complex) | Immune complex deposition | Serum sickness, some autoimmune diseases | Anti-inflammatory drugs |
| Type IV (Delayed) | T cell-mediated | Contact dermatitis, tuberculin reaction | Topical steroids |
Autoimmune Diseases
Immune system attacks body's own tissues
| Disease | Target Tissue | Symptoms | Treatment |
|---|---|---|---|
| Type 1 Diabetes | Pancreatic beta cells | High blood sugar, fatigue | Insulin, immunosuppressants |
| Rheumatoid Arthritis | Joint synovium | Joint pain, inflammation | Anti-inflammatories, biologics |
| Multiple Sclerosis | Nerve myelin | Muscle weakness, vision problems | Immunosuppressants |
| Systemic Lupus | Multiple tissues | Fatigue, joint pain, rash | Corticosteroids, immunosuppressants |
| Celiac Disease | Small intestine | Diarrhea, malabsorption | Gluten-free diet |
Immunodeficiency Disorders
Reduced immune function leading to increased infection risk
Primary Immunodeficiencies (Genetic)
- Severe Combined Immunodeficiency (SCID): Absent T and B cells
- Common Variable Immunodeficiency (CVID): Low antibody production
- DiGeorge Syndrome: Thymus development defect
Secondary Immunodeficiencies (Acquired)
- HIV/AIDS: CD4+ T cell destruction
- Malnutrition: Impaired immune cell function
- Chemotherapy: Bone marrow suppression
- Aging: Immunosenescence, reduced immune function
Laboratory Investigation of Immunity
Blood Tests for Immune Function
Complete Blood Count (CBC):
- White Blood Cell Differential: Neutrophils, lymphocytes, monocytes, eosinophils, basophils
- Abnormalities: Infections, allergies, immunodeficiencies
Specific Immune Tests:
- Antibody Titers: Measure antibody levels against specific antigens
- T Cell Subset Analysis: CD4/CD8 ratios in HIV monitoring
- Complement Levels: Assess complement system function
- Autoantibody Tests: Detect antibodies against self-antigens
Allergy Testing:
- Skin Prick Tests: Localized reaction to allergens
- Blood Tests: IgE levels against specific allergens
- Elimination Diets: Identify food allergies
Immunological Techniques
Microscopy Methods:
- Light microscopy: Visualize immune cells in blood smears
- Fluorescence microscopy: Detect specific antigens with fluorescent antibodies
- Electron microscopy: Detailed examination of immune cell structures
Molecular Methods:
- PCR: Detect pathogen DNA/RNA
- ELISA: Quantify antigens and antibodies
- Flow Cytometry: Analyze immune cell populations
- Western Blotting: Identify specific proteins
Practice Tips for SPM Students
Key Concepts to Master
- Three lines of defense and their specific mechanisms
- Types of immunity (active vs. passive, natural vs. artificial)
- Lymphocyte functions and antigen recognition
- Antibody structure and classes
- Vaccination principles and herd immunity
Experimental Skills
- Identify immune cells from blood smears and diagrams
- Design immunity experiments with proper controls
- Interpret immune test results and clinical significance
- Apply knowledge to vaccination and disease prevention scenarios
Problem-Solving Strategies
- Immune response analysis: Understand the sequence of defense activation
- Vaccination planning: Calculate optimal vaccination schedules
- Disease outbreak analysis: Use herd immunity concepts
- Clinical case studies: Apply immune knowledge to patient scenarios
Environmental and Health Connections
Environmental Impact on Immunity
- Pollution can impair immune function and increase allergy risk
- Climate change affects disease patterns and immune adaptation
- Microbiome diversity influenced by environment and diet
- Stress affects immune system regulation
Public Health Significance
- Vaccination programs prevent millions of deaths annually
- Antibiotic resistance challenges immune system effectiveness
- Pandemic preparedness relies on immune system understanding
- Healthcare worker protection uses immune knowledge for infection control
Biomedical Applications
- Monoclonal antibodies for cancer and autoimmune diseases
- Immunotherapy for cancer treatment
- Stem cell transplantation for immunodeficiencies
- Diagnostic testing for immune function assessment
Summary
- The immune system has three lines of defense: physical barriers, internal cellular defenses, and specific immune responses
- Non-specific immunity provides rapid, broad protection against various pathogens
- Specific immunity involves lymphocytes, antibodies, and immunological memory
- Different types of immunity (active, passive, natural, artificial) provide varying levels and durations of protection
- Vaccination is a safe and effective way to achieve active artificial immunity
- Understanding immunity is crucial for preventing and treating diseases