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46 Cards in this Set
- Front
- Back
Resistance
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Abilities of our bodies to ward off disease through our non specific/specific defenses
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Susceptibility
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Vunerability or lack of defenses
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Innate Immunity (nonspecific resistance)
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defense that protects you against any type of a pathogen "early warning system"
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First line of defense
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intact skin,mucous membranes, normal microbiota
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Second Line of defense
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phagocytes (wbc), inflammation, fever, and antimicrobial substances
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Adaptive Immunity (acquired/specific resistance)
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defense that protects you against very specific pathogens that breach the innate immune system (lymphocytes, tcells, bcells, and antibodies
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skin
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exposed directly to m/o and external objects that can cut abrade tear (vunerable to infection-skin dryness normally can inhibit pathogens)
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mucus membranes
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covers tissues/organs of body cavity exposed to exterior: gastrointestinal tract, respiratory tract
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non physical mechanical factors
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tears, saliva, urine, vaginal secretions, mucus, ciliary escalator
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physical barriers
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skin, mucus membranes
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tears, saliva, urine, vaginal secretions
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wash away m/o that get in abnormal areas
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mucus
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slightly viscous glycoprotein that traps m/o
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ciliary escalator
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lower respiratory tract; propel dust and m/o out of lungs towards your throat; coughing/sneezing speed up escalator
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Chemical factors
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Sebum, lysozyme, gastric juice, transferrins
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sebum
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(oil production, sebaceous glands of skin) unsaturated fatty acids in sebum protective effect against some pathogens/fungi
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lysozyme(in body fluids)
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perspiration, saliva, tears, and nasal secretions (effective at breaking down G+ cell walls=peptidoglycan)
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gastric juice (stomach acid)
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hydrochloric acid, enzymes and mucus (many pathogens/toxins destroyed except toxins of clostridium botulinum and staphylococcus aureus
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Transferrins (Iron binding proteins in blood)
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inhibit bacterial growth by binding iron >too much iron can inhibit phagocytes and result in infection
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Normal Microbiota
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microbaial antagonism (out compete for nutrients and create unfavorable conditions)
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2nd line of defense:
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phagocytes, inflammation, fever, antimicrobial substaces
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phagocytosis (eat cell)
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ingestion of m/o or cellular debris by specif cell type>phagocyte (macrophage)
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inflammation
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damage to body tissue 1.infection 2. physical (sharps, heat, electricity) 3. chemicals (acids bases)
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signs
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visually see
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symptoms
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not apparent to observer
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functions of inflammation
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causative agent and its byproducts removed (if destruction not possible: limit the effects of agent by confining it walling it off, or replace and repair damage tissues)
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stages after tissue damage has occurred
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1. Vasodilation and increased permeability of blood vessels, 2. phagocyte migration and 3. phagocytosis, tissue repair
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Vasodilation
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blood vessels dilate resulting in increased blood flow to the damaged area resulting in redness and heat
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increased vascular permeability
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allowing defensive substances normally found in the blood to enter the injured area which will result in migration of phagocytes and phagocytosis
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chemotaxis
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chemical substances(cytokines) draw the phagocytes to the injury site>within 1 hr of injury and inflammation, phagocytes are on the "scene"
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Margination
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phagocytes in the blood start sticking to the blood vessel wall in response to the cytokines
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emigration (diapedesis)
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phagocytes squeeze through blood vessel endothelium to reach damaged area
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phagocytosis
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of the invading m/o will eventually result in macrophage death after a large # of m/o engulfed >macrophage death >pass until infection subsides
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tissue repair
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tissue is replaced after all harmful substances removed from injury site
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inflammation
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local response (site of contact) to body injury
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fever
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elevated body temp
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systemic:
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spread throughout body
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fever
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systemic response due to bacteria, toxins, viruses that cause hypothalamus (in brain) to raise body temp from 98,6F to replace tissue and increase T cells
(complications: high heart rate, higher metabolic rate, electrolyte imbalances, seizures in young children, delirium, and coma >112-114 F =death |
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Antimicrobial Substances
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complement systems
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complement systems
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defensive system consisting of greater than 30 serum proteins produced by the liver
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cascade even that results in the activation of protein C3:
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classical, lectin, alternative
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classical
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Antibody: Antigen
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Lectin:
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Macrophage ingests bacteria
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Alternative
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complement protein and pathogen
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complement fixation (cytolysis)
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"MAC attack" loss of cellular contents through a transmembrane channel or pore in the m/o c5>c9
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enhancement of inflammation
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blood vessel permeability is increased and chemotactic attraction of phagoctyes by cytokines
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opsonization
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C3b coating different m/o results in enhanced phagocytosis
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