BY 312 Lecture (3/27)
Overview of the Immune System
Innate Immunity
Phagocytes and Phagocytosis
Discussion on the role of phagocytes, particularly wandering and mixed macrophages, in innate immunity.
Phagocytosis involves several steps:
Chemotaxis: Chemically stimulated movement of phagocytes toward damaged tissues, facilitated by chemicals produced by microbes.
Adherence: Attachment of phagocytes to microbes or foreign materials.
Ingestion: Phagocytes use pseudopods to engulf and internalize microbes, forming a phagosome.
Digestion: Merging of the phagosome with lysosomes creates a phagolysosome, where microorganisms are broken down.
Killing Phase: Remaining indigestible material is termed a residual body, which is then recycled.
Natural Killer Cells: Discussion on these cells' role in innate immunity, especially in relation to phagocytosis.
Endogenous Antimicrobials (AMPs): These antimicrobial proteins are produced by neutrophils and macrophages to assist in the immune response.
Defensins: A well-known type of AMP exhibiting broad-spectrum antimicrobial activity.
Complement System:
Described as a group of inactive proteins that, once activated, enhances immune reactions by attacking cell walls, attracting phagocytes, and stimulating inflammation.
Iron Binding Proteins: Inhibit bacterial growth by reducing available iron.
Interferons: Proteins released by virus-infected cells that activate immune responses to prevent viral replication.
Types of interferons discussed: alpha, beta, and gamma.
Phagocytosis Revisited
Detailed steps of phagocytosis re-emphasized, linking to previous discussions and emphasizing critical processes like oxidative bursts and the creation of residual bodies.
Fever and Inflammation
Fever
Defined as an abnormally high body temperature caused by resetting the hypothalamic thermostat.
Functions of fever include:
Speeding up body reactions.
Enhancing the effects of endogenous antimicrobials.
Mobilization of defenses and acceleration of tissue repair.
Inhibition of pathogens.
Inflammation
A generalized defensive response to tissue damage from various causes (infections, burns, cuts).
Common signs of inflammation:
Redness (increased blood flow)
Pain (chemical stimulation of pain receptors)
Heat (due to increased blood flow)
Swelling (fluid accumulation at the site)
Stages of Inflammation
Three basic stages of inflammation:
Vasodilation: Increases blood flow and permeability.
Emigration: Movement of phagocytes from blood vessels into interstitial spaces to site of damage.
Tissue Repair: Involves removal of toxins and debris, and re-establishment of normal tissue function.
Additional Inflammatory Mediators
Mention of histamines, kinins, prostaglandins, leukotrienes, and complements as crucial players in the inflammatory response.
Role of kinins in chemotaxis.
Prostaglandins enhance other mediators.
Sensitization and Pain
Pain as a key signal for inflammation, helping to alert the body of injury.
Importance of pain in promoting protective behavior (avoiding further harm).
Types of Inflammation
Acute Inflammation: Rapid onset, lasts days to weeks, characterized by immediate response to tissue damage.
Chronic Inflammation: Slow, prolonged response lasting months or years, exemplified by conditions like rheumatoid arthritis and peptic ulcers.
Chronic inflammation can lead to continued pain and immobility due to sensitization of nerve endings.
Summary of Key Concepts
Immune Response
Review of components involved in innate immunity, including:
AMPs,
Natural killer cells,
Complement system,
Iron binding proteins, and interferons.
Transition to Adaptive Immunity
Introduction to adaptive immunity, defined as the body's ability to specifically respond to foreign antigens.
Key characteristics of adaptive immunity include:
Specificity: Ability to distinguish between self and non-self through antigens (MHC).
Memory: Previously encountered antigens result in quicker and more vigorous immune responses during future attacks.
Definition of antigens as foreign substances that trigger an immune response, clarifying that not all foreign materials are antigenic.
Explanation of epitopes as specific sites on antigens that initiate immune responses.
Closure with emphasis on the significance of learning about both adaptive and acquired immune responses in future classes, hinting at an upcoming discussion on vaccines.