BackChapter 43: Immunology – Innate and Adaptive Immune Responses
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Immunology: Overview
Immunology is the study of the immune system, which protects organisms from infection by recognizing and responding to pathogens. The immune system is divided into two main branches: innate immunity and adaptive immunity.
Innate and Adaptive Immunity
Comparison of Innate and Adaptive Immunity
Innate Immunity:
Present from birth; acts immediately upon infection.
Non-specific: recognizes traits shared by broad ranges of pathogens using a small set of receptors.
Includes physical barriers (skin, mucous membranes), chemical defenses, and blood cells.
Rapid response.
Adaptive (Acquired) Immunity:
Develops after exposure to pathogens.
Highly specific: recognizes specific features of particular pathogens using a vast array of receptors.
Involves lymphocytes (B cells and T cells).
Slower initial response, but generates memory cells for rapid future responses.
Table: Innate vs. Adaptive Immunity
Feature | Innate Immunity | Adaptive Immunity |
|---|---|---|
Specificity | Non-specific | Highly specific |
Response Time | Immediate | Slower (days to weeks) |
Memory | None | Immunological memory |
Main Cells | Phagocytes, NK cells | B cells, T cells |
Concept 1: Innate Immunity
Recognition and Response in Innate Immunity
Relies on traits common to groups of pathogens.
Types of phagocytic cells:
Neutrophils: Engulf and destroy pathogens; attracted to infection sites.
Macrophages: Large phagocytes found throughout the body; also activate adaptive immunity.
Dendritic cells: Activate adaptive immunity by presenting antigens.
Eosinophils: Produce destructive enzymes, especially against parasites.
Lymphatic system: Network that distributes lymph (fluid) and houses immune cells.
Inflammatory Response
Localized response to injury or infection, characterized by redness, swelling, heat, and pain.
Mast cells release histamine, increasing blood vessel permeability.
Macrophages and neutrophils release cytokines to enhance the immune response.
Pus: Accumulation of white blood cells, dead pathogens, and cell debris.
The Complement System
Composed of about 30 proteins in blood, usually inactive.
Functions:
Opsonization: Enhances phagocytosis.
Activates mast cells: Promotes inflammation.
Cytolysis: Forms pores in pathogen membranes, causing lysis.
Neutralizes antigens.
Concept 2: Adaptive Immunity
Pathogen-Specific Recognition
Relies on lymphocytes:
B cells: Mature in bone marrow.
T cells: Mature in thymus.
Key characteristics:
Diversity: Billions of antigen receptors.
Self-tolerance: Avoids attacking self.
Proliferation: Clonal selection after activation.
Immunologic memory: Enhanced response to repeated exposure.
Antigen Recognition
Antigen: Substance that elicits a lymphocyte response.
Epitope: Specific part of antigen recognized by receptors.
B and T cell receptors have similar components but recognize antigens differently.
B Cell Receptors and Antibodies
B cell receptor: Y-shaped, with two heavy and two light chains.
Constant (C) region: Little variation among B cells.
Variable (V) region: High diversity, provides antigen specificity.
Activated B cells secrete antibodies (immunoglobulins, Ig).
T Cell Receptors and MHC
T cell receptor: Two polypeptide chains (α and β).
Recognizes antigen fragments presented by MHC (major histocompatibility complex) on host cells.
Antigen presentation: Process of displaying antigen fragments on cell surface via MHC.
Concept 3: Adaptive Immunity Defends Against Infection
Branches of Acquired Immunity
Humoral immune response:
Antibodies neutralize or eliminate toxins and pathogens in blood and lymph.
Cell-mediated immune response:
Specialized T cells destroy infected host cells.
Helper T cells activate both humoral and cell-mediated responses.
Antibody Functions
Opsonization: Enhances phagocytosis.
Complement activation: Triggers protein cascade, leading to cell lysis.
Attack complex: Forms pores in foreign cell membranes.
Neutralization: Blocks pathogen/toxin from binding to host cells.
Immunity Types
Active immunity:
Develops after exposure to antigen (natural infection or vaccination).
Involves memory cell formation.
Passive immunity:
Immediate, temporary protection (e.g., maternal antibodies via placenta or breast milk).
Classes of Immunoglobulins (Antibodies)
IgD: Membrane-bound form.
IgM: First soluble class produced.
IgG: Most abundant, second soluble class.
IgA and IgE: Other soluble classes with specialized functions.
Concept 4: Disruptions in Immune System Function
Allergies
Exaggerated immune responses to harmless antigens (allergens).
IgE antibodies bind to mast cells, triggering histamine release.
Severe reactions can cause anaphylactic shock.
Autoimmune Diseases
Immune system attacks body's own cells.
Examples: lupus, rheumatoid arthritis, type 1 diabetes, multiple sclerosis.
Other Factors Affecting Immunity
Moderate exercise enhances immune function.
Psychological stress and lack of rest can impair immunity.
HIV and Immune System Suppression
HIV infects helper T cells, impairing both humoral and cell-mediated responses.
Leads to AIDS due to loss of immune function.
HIV evades immunity via antigenic variation and latency.
Cancer and Immunity
Impaired adaptive immunity increases cancer risk.
Some cancers are virus-associated (e.g., HPV and cervical cancer).
Vaccines can prevent certain virus-induced cancers.
Key Terms and Concept Map Suggestions
Lymphocyte, antigen, receptor, helper T cell, B cell, cytotoxic T cell, memory cell, antigen-presenting cell (APC), plasma cell, MHC class I/II, heavy chain, light chain, variable region, constant region, CD4, macrophage, phagocytosis, humoral response, cell-mediated response.