Skip to main content
Back

Adaptive Immunity: Mechanisms and Disorders

Study Guide - Smart Notes

Tailored notes based on your materials, expanded with key definitions, examples, and context.

Adaptive Immunity

Overview of Adaptive Immunity

Adaptive immunity is a specific defense mechanism that targets particular pathogens and provides long-lasting protection through memory. It is characterized by its specificity and ability to remember previous encounters with pathogens, resulting in a faster and more effective response upon re-exposure.

  • Specificity: Immune responses are tailored to specific antigens.

  • Memory: Upon re-exposure to the same antigen, the immune system responds rapidly, often preventing illness.

Types of Adaptive Immunity

Humoral vs. Cellular Immunity

Adaptive immunity is divided into two main branches: humoral immunity and cellular immunity.

  • Humoral Immunity: Mediated by B lymphocytes (B cells) and antibodies. Effective against extracellular pathogens.

  • Cellular Immunity: Mediated by T lymphocytes (T cells). Effective against intracellular pathogens and abnormal cells.

Types of humoral immunity: active and passive, naturally and artificially acquired

Antigens and Epitopes

Definition and Properties

Antigens are substances that trigger an immune response, typically by stimulating the production of antibodies. The immune system recognizes specific regions on antigens called epitopes or antigenic determinants.

  • Complexity: More complex molecules (e.g., proteins) are more antigenic than simpler ones (e.g., lipids).

  • Multiple Epitopes: A single antigen can have several epitopes, each recognized by a different antibody.

Antigen with multiple epitopes and antibody binding sites

B Lymphocytes (B Cells)

Development and Selection

B cells develop in the red bone marrow, where they undergo selection to ensure they do not react to self-antigens. Self-reactive B cells are destroyed, and the remaining cells colonize lymphatic organs.

  • Development Site: Red bone marrow

  • Selection: Elimination of self-reactive B cells

  • Colonization: Lymph nodes, spleen, and other lymphatic tissues

B lymphocyte under microscope

B Cell Activation

When a B cell encounters its specific antigen, it becomes activated, proliferates, and differentiates into plasma cells (which secrete antibodies) and memory B cells (which provide long-term immunity).

Diagram of B cell activation and differentiation

Antibody Structure and Classes

Antibody Structure

Antibodies, also known as immunoglobulins (Ig), are Y-shaped proteins composed of four polypeptide chains: two heavy and two light chains. Each antibody has variable regions for antigen binding and constant regions that determine its class and function.

  • Variable (V) regions: Bind to specific antigens

  • Constant (C) regions: Define antibody class and mediate effector functions

  • Disulfide bonds: Stabilize the antibody structure

Antibody structure with labeled regions

Antibody Classes

There are five main classes of antibodies, each with distinct structures and functions:

  • IgG: Monomer; most abundant in circulation; crosses placenta; secondary immune response

  • IgD: Monomer; B cell receptor

  • IgE: Monomer; binds to mast cells; involved in allergic responses

  • IgA: Monomer in plasma, dimer in secretions; protects mucosal surfaces

  • IgM: Pentamer; first antibody produced in primary response

Antibody classes: IgG, IgD, IgE, IgA, IgM

Humoral Immune Response

Primary and Secondary Responses

The humoral immune response involves the production of antibodies by plasma cells. The primary response occurs upon first exposure to an antigen, while the secondary response is faster and stronger due to memory B cells.

  • Primary Response: Slow, produces memory B cells

  • Secondary Response: Rapid, prevents illness

Graph of primary and secondary antibody responses Diagram of B cell activation and memory

Cellular Immunity

T Lymphocytes (T Cells)

T cells are responsible for cell-mediated immunity, targeting infected or abnormal cells. There are three main types:

  • Cytotoxic T cells (Tc, CD8): Destroy infected or cancerous cells

  • Helper T cells (Th, CD4): Activate B cells and other immune cells

  • Memory T cells (Tm): Provide long-term immunity

Development and Maturation

T cells originate in the red bone marrow and mature in the thymus. Self-reactive T cells are eliminated during maturation. Mature T cells colonize lymphatic tissues and organs.

Thymus and spleen in the human body Bone marrow in the femur

T Cell Activation and Function

When a T cell encounters its specific antigen presented by an antigen-presenting cell (APC), it becomes activated, proliferates, and differentiates into effector and memory cells.

T cell attacking a target cell Diagram of T cell development and activation

Antigen Processing and Presentation

Role of Antigen-Presenting Cells (APCs)

APCs such as B cells and macrophages ingest antigens, process them, and present antigen fragments on their surface using major histocompatibility complex (MHC) molecules. This is essential for T cell activation.

  • MHC I: Present on all nucleated cells; present endogenous antigens

  • MHC II: Present on APCs; present exogenous antigens

Antigen processing and presentation by APCs

T Cell Activation

Mechanism of Activation

T cells recognize antigens presented by APCs via MHC molecules. This interaction stimulates the proliferation of T cell clones and the formation of memory cells. Helper T cells secrete interleukins to coordinate immune responses.

Diagram of T cell activation and clonal selection

Immune System Disorders

Hypersensitivity (Allergy)

Hypersensitivity is an excessive immune response to harmless antigens (allergens). Anaphylactic shock is a severe, life-threatening allergic reaction characterized by bronchiole constriction, vasodilation, and shock. Treatment includes epinephrine administration.

Diagram of allergic response and anaphylaxis

Autoimmune Diseases

Autoimmune diseases occur when the immune system fails to recognize self-antigens and attacks the body's own tissues. Examples include type I diabetes mellitus, lupus, and rheumatoid arthritis. Mechanisms may involve cross-reactivity, structural changes in self-antigens, or environmental triggers.

Body parts affected by autoimmune diseases

Acquired Immunodeficiency Syndrome (AIDS)

AIDS is caused by the human immunodeficiency virus (HIV), which primarily infects helper T cells (CD4+). A decline in helper T cell count (< 200 cells/μL) leads to increased susceptibility to infections and cancers.

Structure of HIV virus

Summary Table: Antibody Classes

Class

Structure

Main Function

IgG

Monomer

Main antibody in secondary response; crosses placenta

IgM

Pentamer

First antibody in primary response

IgA

Dimer (in secretions)

Protects mucosal surfaces

IgE

Monomer

Involved in allergies and parasitic infections

IgD

Monomer

B cell receptor

Key Terms

  • Antigen: Substance that triggers an immune response

  • Epitope: Specific region of an antigen recognized by antibodies

  • Antibody (Immunoglobulin): Protein produced by B cells that binds to antigens

  • APC (Antigen-Presenting Cell): Cell that processes and presents antigens to T cells

  • MHC (Major Histocompatibility Complex): Molecules that display antigen fragments on cell surfaces

  • Memory Cell: Long-lived immune cell that responds rapidly upon re-exposure to antigen

Pearson Logo

Study Prep