Biology -Entrance Exam ( Universidad de Navarra) - unit 6 (1)
Unit 7 - Immunology
Introduction to Immunology
Definition: The study of how the body protects itself against infectious diseases from microorganisms (bacteria, viruses, protozoa, fungi) and parasites (helminths).
Initial Barriers: Physical barriers like skin, and substances like saliva and tears neutralize bacteria.
Mucosal tissues protect internal areas (e.g., lungs, gut) with mucus that traps pathogens.
Cilia in airways transport contaminants away.
Immune System Overview
Components:
Innate Immune System: Provides rapid, general responses to infections.
Adaptive Immune System: Develops specific responses and immune memory.
Both systems work cooperatively; the innate system alerts the adaptive system.
Immune Tissues
Origin of immune cells: Bone marrow (hematopoietic stem cells).
T Lymphocytes: Mature in the thymus (primary lymphoid tissue).
Secondary Lymphoid Tissues:
Lymph Nodes: Monitor lymph for infection.
Spleen: Acts like a lymph node for blood.
MALT: Important for mucosal immune responses (gut, airways).
Innate Immunity
Key Cells and Mechanisms
Mast Cells & Basophils: Activated to secrete histamine, involved in inflammatory responses.
Phagocytes:
Neutrophils and Macrophages: Respond to infection, perform phagocytosis (engulf pathogens).
Pattern Recognition: Uses Pattern Recognition Receptors (PRRs) like Toll-like receptors (TLRs) to identify pathogens.
Complement System
Composed of proteins that enhance the immune response.
Complement Pathways:
Classical, alternative, and mannose-binding lectin pathways.
Adaptive Immunity
Lymphocytes
T Lymphocytes (T Cells): Mature in the thymus.
B Lymphocytes (B Cells): Mature in bone marrow.
Each cell becomes specific to a unique antigen.
Helper T Cells: Activate and shape immune responses; classified into subtypes (Th1, Th2, Th17).
Antigen-Presenting Cells (APCs)
Major APCs: Dendritic cells, macrophages, B cells.
Process and present antigens to T cells via MHC molecules.
Cellular and Humoral Responses
Cellular Response: Cytotoxic T cells target infected or malignant cells.
Humoral Response: B cells produce antibodies following T cell activation.
Immune Memory
Memory Cells: Formed after primary response for quick reactivation upon re-exposure to pathogens.
Cytokines: Proteins facilitating communication in immune responses.
Immune Dysfunction
Types
Inborn Immunodeficiencies: Genetic disorders like Severe Combined Immunodeficiency (SCID).
Autoimmunity: Immune system attacks self-tissues (e.g., rheumatoid arthritis).
Pathologies
Autoimmune Diseases: Includes type 1 diabetes, multiple sclerosis.
Nonspecific Innate Immunity
Physical Defenses
Barriers: Skin, mucous membranes prevent pathogen entry.
Skin Structure: Epidermis protects through keratin production.
Chemical Defenses
Sebum: Oil secreted by skin, provides additional barriers.
Enzymes: Salivary and digestive enzymes eliminate pathogens.
Antigen Definition & Properties
Antigen: A substance that can trigger an immune response. Includes proteins, carbohydrates, and other molecules recognized as foreign.
Characteristics of Antigens
Foreign Nature: Recognized as non-self.
Chemical Nature: Proteins are highly immunogenic, while polysaccharides are moderate.
Molecular Size: Immunogenicity generally requires a size >5000 Da.
Complexity and Rigidity: More complex and rigid molecules are more immunogenic.
Molecular Determinants: Antigenic determinants (epitopes) bind to antibody receptors.
Types of Antigens
Exogenous Antigens: From outside the host (e.g., pathogens).
Endogenous Antigens: Produced within the host's own cells (e.g., from normal metabolism).
Autoantigens: Body's own proteins mistaken for foreign (causing autoimmune diseases).
Tumor Antigens: Unique surfaces of cancer cells triggered by mutations.
Production of Monoclonal Antibodies
Overview
Monoclonal Antibodies (mAbs): Engineered from single B cell clones targeting specific antigens.
Types:
Murine, Chimeric, Humanized, and Fully Human.
Applications
Treatment of cancers, autoimmune diseases, and diagnostic tools.
Limitations
Risk of immune responses to non-human components (e.g., HAMA reaction).
Mechanisms of Immune Response
Recognition: Identification of foreign antigens.
Activation: Initiation of immune responses.
Attack: Targeting and elimination of pathogens.
Control: Regulation and resolution of immune reactions after pathogen elimination.