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46 Cards in this Set

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