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The Immune System: Innate and Adaptive Defenses

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Chapter 24: The Immune System

Introduction: Viruses, Cancer, and Immunity

Viruses can cause certain cancers, such as cervical and anal cancers caused by the human papillomavirus (HPV). Vaccines are available to prevent HPV infection, but the duration of their effectiveness is still under study.

A person receiving a vaccine injection in the upper arm

Innate Immunity

24.1 All Animals Have Innate Immunity

Innate immunity provides the first line of defense against pathogens—agents that cause disease. It acts immediately upon infection and is the same regardless of prior exposure to the pathogen. Invertebrates rely solely on innate immunity, while vertebrates possess both innate and adaptive immunity.

  • Barriers: Skin, mucous membranes, acidic environments, secretions, and cilia prevent pathogen entry.

  • Internal Defenses: If barriers are breached, phagocytic cells (neutrophils, macrophages), natural killer cells, defensive proteins (e.g., interferons), and the inflammatory response act to eliminate pathogens.

Diagram of innate external and internal barriers

24.2 The Inflammatory Response Disinfects Damaged Tissue

The inflammatory response is triggered by tissue damage, such as a splinter, and helps disinfect tissues and limit further infection. The process involves:

  1. Release of signaling molecules from mast cells and macrophages, causing nearby capillaries to dilate.

  2. Capillaries become leaky, allowing neutrophils to migrate to the infection site.

  3. Neutrophils digest bacteria and cell debris, leading to tissue healing.

Step 1: Tissue injury and signaling molecule release Step 2: Capillary dilation and neutrophil migration Step 3: Neutrophil phagocytosis and tissue healing

Adaptive Immunity

24.3 The Adaptive Immune Response Counters Specific Invaders

Adaptive (acquired) immunity is found only in vertebrates and is activated after exposure to specific pathogens. It is highly specific and has memory, allowing for a stronger response upon re-exposure to the same pathogen.

  • Antigen: Any molecule that elicits an adaptive immune response.

  • Antibody: A protein in blood plasma that binds to a specific antigen and helps counter its effects.

Comparison of innate and adaptive immune responses

24.4 The Lymphatic System: A Crucial Battleground

The lymphatic system is involved in both innate and adaptive immunity. It consists of lymphatic vessels, lymph nodes, and lymph (a fluid similar to interstitial fluid but with fewer nutrients and less oxygen). Lymph organs are packed with white blood cells that fight infections.

  • Main functions: Return tissue fluid to the circulatory system and fight infection.

Diagram of the lymphatic system and lymph node structure

24.5 Lymphocytes Mount a Dual Defense

Lymphocytes originate from stem cells in the bone marrow. B lymphocytes (B cells) mature in the bone marrow, while T lymphocytes (T cells) mature in the thymus. B and T cells defend against infections in body fluids and inside cells, respectively.

  • Humoral immune response: B cells produce antibodies that act against free-floating antigens in body fluids.

  • Cell-mediated immune response: T cells attack infected cells directly.

Development of B and T lymphocytes from stem cells

24.6 Antigen Receptors and Antibodies Bind to Specific Regions on an Antigen

B cells bind antigens directly, while T cells require antigen presentation. The specific part of an antigen recognized by antibodies or antigen receptors is called the epitope. The region on the antibody or receptor that binds the epitope is the antigen-binding site.

Antibodies binding to epitopes on an antigen

24.7 Clonal Selection Mobilizes Defensive Forces

Clonal selection is the process by which an antigen activates only those lymphocytes with receptors specific for that antigen. These selected cells multiply into effector cells (which combat the antigen) and memory cells (which provide long-term immunity).

  • Effector cells: Short-lived cells that secrete antibodies or attack infected cells.

  • Memory cells: Long-lived cells that respond rapidly upon re-exposure to the antigen.

Clonal selection: formation of effector and memory cells Clonal selection: memory cells and effector cells

24.8 Primary and Secondary Immune Responses

The primary immune response occurs upon first exposure to an antigen and is slower and weaker. The secondary immune response is faster, stronger, and longer-lasting due to the presence of memory cells.

Graph comparing primary and secondary immune responses

24.9 Herd Immunity

Herd immunity occurs when a high percentage of the population is vaccinated, preventing the spread of infectious diseases even to unvaccinated individuals. This is the rationale for mandatory vaccinations in public health policy.

Diagram illustrating herd immunity versus no herd immunity

24.10 The Structure and Function of Antibodies

Antibodies do not kill pathogens directly but mark them for destruction by forming antigen-antibody complexes. Antibodies have specific antigen-binding sites that match the shape of their target antigen.

Structure of an antibody and its antigen-binding sites Mechanisms of antibody action: neutralization, agglutination, complement activation

24.11 Measuring Vaccine Effectiveness

Scientists measure antibody levels to assess the duration of vaccine-induced immunity. For HPV vaccines, studies track the persistence of anti-HPV-16 and anti-HPV-18 antibodies over several years.

Graph of antibody levels after HPV vaccination with Gardasil and Cervarix

24.12 Helper T Cells Stimulate Immune Responses

Helper T cells are activated when they recognize a complex of a foreign antigen and a self protein on an antigen-presenting cell. Once activated, helper T cells stimulate both B cells (humoral response) and cytotoxic T cells (cell-mediated response).

Helper T cell activation by antigen-presenting cell

24.13 Cytotoxic T Cells Destroy Infected Body Cells

Cytotoxic T cells recognize infected cells by binding to self-nonself complexes on their surfaces. They release perforin, which forms pores in the infected cell's membrane, and enzymes that induce cell death. This process eliminates the pathogen's reservoir and exposes antigens to antibodies.

Cytotoxic T cell attacking an infected cell

24.14 HIV and AIDS

HIV infects and destroys helper T cells, severely compromising the immune system and leading to AIDS. This makes patients susceptible to opportunistic infections and certain cancers. Antiviral drugs can slow disease progression but do not cure AIDS.

Human helper T cell infected with HIV (colorized TEM)

24.15 Evolution of HIV

HIV mutates rapidly due to the lack of proofreading by reverse transcriptase, leading to the emergence of drug-resistant strains and complicating treatment efforts.

24.16 Self-Recognition and MHC Molecules

Lymphocytes distinguish self from nonself using major histocompatibility complex (MHC) molecules, which are unique to each individual. This system is crucial for immune function but complicates organ transplantation due to the risk of rejection.

Disorders of the Immune System

24.17 Immune System Disorders

  • Autoimmune disorders: The immune system attacks self molecules (e.g., rheumatoid arthritis, type 1 diabetes).

  • Immunodeficiency disorders: Components of the immune system are missing or nonfunctional, leading to frequent infections (e.g., SCID, AIDS).

Thermal image of hands showing inflammation in autoimmune disease

24.18 Allergies: Overreactions to Environmental Antigens

Allergies are hypersensitive responses to harmless antigens (allergens). The reaction involves two stages: sensitization (initial exposure) and later exposure, which triggers histamine release and allergy symptoms. Antihistamines can provide temporary relief.

Sequence of events in an allergic reaction Sensitization: initial exposure to an allergen Later exposure: allergen binds to antibodies on mast cell, histamine released

Summary Table: Innate vs. Adaptive Immunity

Feature

Innate Immunity

Adaptive Immunity

Response Time

Immediate

Slower (days)

Specificity

Broad

Highly specific

Memory

None

Yes

Main Components

Barriers, phagocytes, NK cells, complement

B cells, T cells, antibodies

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