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Vocabulary flashcards covering key concepts from the lecture on non-specific host resistance, including barriers, innate defenses, phagocytosis, inflammation, antimicrobial substances, and interferons.
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Resistance
The ability to ward off diseases through host defenses (also called immunity).
Susceptibility
Lack of resistance or vulnerability to infection.
Non-specific resistance
Defenses that protect against pathogens regardless of species (innate immunity).
First Line of Defense
Non-specific natural barriers that restrict entry of pathogens (e.g., skin, mucous membranes, secretions).
Second Line of Defense
Innate, non-specific immune defenses that provide a rapid local response after entry (e.g., fever, phagocytes, inflammation, interferons).
Third Line of Defense
Antigen-specific immune responses (adaptive immunity) including antibodies and lymphocytes.
Skin barrier
Intact skin acts as a mechanical barrier preventing pathogen entry.
Epidermis
Outer skin layer; contains Langerhans cells; keratin makes skin waterproof and less hospitable to microbes.
Dermis
Thicker inner skin layer with connective tissue; infections are rarer in intact skin.
Mucous membranes
Secretions trap microbes and limit adhesion; part of first line of defense.
Ciliary escalator
Cilia move debris out of the respiratory tract; helps expel microorganisms via sneezing or coughing.
Epiglottis
Flap that covers the glottis during swallowing to protect the airway from material entering the lower airway.
Urine
Mechanical clearance of organisms by voiding; urinary tract flushed of microbes.
Sebum
Secreted by sebaceous glands; fatty acids inhibit bacterial growth on the skin.
Perspiration
Sweat; contains lysozyme, contributing to antibacterial activity.
Lysozyme
Enzyme that breaks down bacterial cell walls (peptidoglycan); found in tears, saliva, mucus, and sweat.
Gastric juice
Stomach acid (HCl, pH ~1–2) that kills many ingested microbes.
Transferrin
Iron-binding protein that reduces free iron and limits bacterial growth.
Microbial antagonists (Normal flora)
Normal microbiota that prevent pathogen colonization; can become pathogenic if balance is disrupted.
Candida albicans
Opportunistic fungus; part of vaginal/GI flora that can cause candidiasis when balance is disrupted.
Bacteriocin
Toxin produced by normal flora that inhibits growth of other bacteria (e.g., some E. coli).
Leukocytes (white blood cells)
Formed elements of blood involved in defense; increase (leukocytosis) or decrease (leukopenia) during infections.
Platelets
Blood cells that form clots to seal wounds (hemostasis).
Neutrophils
Polymorphonuclear leukocytes; highly phagocytic; first to arrive at infection; major acute responders.
Basophils
Leukocytes that release histamine; involved in inflammation and allergic responses.
Eosinophils
Leukocytes that respond to parasites and are involved in certain hypersensitivity reactions; moderately phagocytic.
Monocytes
Mononuclear phagocytes; become macrophages when in tissues; phagocytic.
Macrophages
Fixed (e.g., Kupffer cells in liver) or wandering phagocytes that digest microbes; key in later inflammation stages.
Phagocytosis
Non-specific engulfing and digestion of microbes by phagocytes; steps include adhesion, ingestion, digestion, and phagolysosome formation.
Adherence (phagocytosis step)
Attachment of the phagocyte to the microbe, often enhanced by opsonization.
Opsonization
Coating of microbes with antibodies (IgG) or C3b to enhance phagocytosis.
Ingestion
Phagosome formation as the microbe is taken into the phagocyte.
Digestion
Destruction of ingested microbes inside a phagolysosome by enzymes and reactive species.
Phagolysosome
Vesicle formed when a phagosome fuses with a lysosome for microbe digestion.
Chemotaxis
Migration of phagocytes toward a site of infection in response to chemical signals (e.g., C5a, IL-8, f-Met).
Margination
Leukocytes adhere to the inner surface of blood vessels before diapedesis.
Emigration/Diapedesis
Movement of leukocytes through vessel walls into surrounding tissue.
Inflammation
Defensive tissue response to injury or infection; aims to contain and destroy pathogens and begin tissue repair.
Cardinal signs of inflammation
Pain (dolor), Heat (calor), Redness (rubor), Swelling (tumor), Loss of function.
Vasodilation
Widening of blood vessels increasing blood flow and permeability during inflammation.
Histamine
Mediator causing vasodilation and increased vascular permeability during inflammation.
Kinins, Prostaglandins, Leukotrienes
Inflammatory mediators that modulate vasodilation and permeability and recruit immune cells.
Complement system
Group of serum proteins activated via classical or alternative pathways; leads to cytolysis (MAC), inflammation, and opsonization.
Classical pathway
Complement activation triggered by antibodies bound to antigen.
Alternative pathway
Complement activation triggered directly by microbial surfaces, without antibodies.
C3
Central component of complement activation; its cleavage drives downstream events.
Membrane Attack Complex (MAC)
C5b-9 complex that forms pores in microbial membranes causing lysis.
Cytolysis
Lysis of pathogens due to MAC formation and membrane disruption.
Opsonization (complement context)
C3b coating that enhances phagocytosis by phagocytes.
Interferons
Antiviral proteins that interfere with viral replication and protect neighboring cells.
Interferon alpha and beta
Produced by virus-infected cells; induce antiviral proteins in neighboring cells.
Interferon gamma
Produced by lymphocytes; activates macrophages and increases MHC expression.
AVPs (antiviral proteins)
Proteins induced by interferons that inhibit viral replication in neighboring cells.
Fever (pyrexia)
Abnormally high body temperature; mediated by hypothalamus and IL-1; can inhibit pathogens and aid repair but may cause dehydration or electrolyte imbalance.
Interleukin-1 (IL-1)
Cytokine associated with fever and the inflammatory response.
Hypothalamus
Brain region that regulates body temperature; modulated during fever.
Tissue repair (stroma vs parenchyma)
Repair processes: stroma (supporting tissue) and parenchyma (functional tissue) regenerate after injury.
Secretory structures and secretions (overview)
Secretions and structures that contribute to barrier defenses (e.g., lacrimal glands, salivary glands, mucus, ciliary action, epiglottis, peristalsis, urination, acidic vaginal secretions).
Lacrimal gland
Tear production; washes and dilutes microbes on the eye surface.
Salivary glands
Saliva washes microbes from teeth and mucous membranes and contains IgA and lysozyme.
Nose hairs and mucus
Filter and trap inhaled particles and microbes.
Mucus
Thick secretion that traps microbes; cleared by ciliary action.
Genito-urinary secretions
Vaginal secretions are acidic and help maintain protection; urination flushes the urethra.
Gastric acidity
Low pH of gastric juice (HCl) that kills many ingested pathogens.