innate immunity Flashcards

1
Q

define immune system

A

cells and organs that contribute to immune defences against infectious and non infectious (cancer) conditions

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2
Q

define infectious disease

A

when the pathogen succeeds in evading and/or overwhelming the host’s immune defences

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3
Q

what are the roles of the immune system

A

pathogen recognition
containing/eliminating the infection
regulating itself- minimum damage to self
remembering pathogens

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4
Q

what are the two types of immune response and what’s the difference

A

innate immunity and adaptive immunity
innate- immediate protection:fast, lack of specificity and memory, no change in intensity
adaptive- long lasting protection:slow, specificity, immunologic memory, changes in intensity

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5
Q

what barriers does innate immunity consist of?

A

physical
physiological
chemical
biological

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6
Q

what are the physical barriers provided by innate immunity?

A

skin
mucous membranes- mouth, respiratory tract, GI tract &urinary tract
bronchial cilia

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7
Q

what are the physiological barriers provided by innate immunity?

A

diarrhoea- food poisoning
vomiting- food poisoning, hepatitis, meningitis
coughing- pneumonia
sneezing -sinusitis

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8
Q

what are the chemical barriers

A
low pH 
antimicrobial molecules- IgA(immunoglobin A):tears, saliva, mucous membrane)
lysozyme (sebum, sweat,urine)
mucus 
beta-defensins(epithelium)
gastric acid +pepsin
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9
Q

what are the biological barriers

A

normal flora in strategic locations

absent in internal organs/tissues

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10
Q

what are the benefits of normal flora

A

compete with pathogens for attachment sites and resources.
produce antimicrobial chemicals
synthesise vitamins (K ,B12, other B vitamins)

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11
Q

how can normal flora cause clinical problems

A

when they are displaced from normal location to sterile location
breaching skin integrity- skin loss(burns), surgery, IV lines, skin diseases , injection drug users and tattoo/piercing
fecal-oral route
fecal-perineal-urethral route (UTI)
poor dental hygiene/dental work

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12
Q

what are the second lines of defence(innate immunity)

A

phagocytes and chemicals causing inflammation

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13
Q

what are the main types of phagocytes

A

macrophages , monocytes and neutrophils

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14
Q

function of macrophages

A

present in all organs.
phagocytosis- ingest and destroy microbes
present microbial antigens to T cells
produce cytokines/chemokines

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15
Q

function of monocytes

A

recruited at infection site and differentiate into macrophages

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16
Q

function of neutrophils

A

recruited by chemokine to site of infection

ingest and destroy pyogenic bacteria

17
Q

name cells other than phagocytes involved in innate immunity

A

basophils/mast cells
eosinophils
natural killer cells
dendritic cells

18
Q

how do phagocytes recognise pathogen

A

microbial structures have pathogen-associated molecular patterns(PAMPs):carbs, lipids.proteins &nucleic acids
Phagocytes have pathogen recognition receptors (PRRs):toll like receptors
opsonisation -coating proteins called opsonins that bind to the microbial surfaces leading to enhanced attachment of phagocytes and clearance of microbes

19
Q

name some examples of opsonins

A

complement proteins- C3b, C4b
antibodies-IgG,IgM
Acute phase proteins: C-reactive protein(CRP), Mannose-binding lectin(MBL)

20
Q

how do phagocytes destroy microbes

A

once the phagocyte has recognised and bound to the microbe via PAMP to PRR interactions and the opsonin to opsonin receptor interactions it can now be destroyed by engulfment and digestion.
this can either happen by an oxygen dependant pathway- free oxygen radicals
or a oxygen independent pathway- enzymatic digestion

21
Q

name some proteins from the complement system and their function

A

C3a and C5a- recruitment of phagocytes
C3b- opsonisation of pathogens
C5-C9: killing of pathogens via membrane attack complex

22
Q

state some antimicrobial actions of cytokines

A

liver-produce CRP &MBL
bone marrow - neutrophil mobilisation
hypothalmus -increase body temp
blood vessels -vasodilation, vascular permeability and expression of adhesion molecules

23
Q

State some clinical problems when phagocytosis is reduced

A

decrease spleen function- asplenic and hyposplenic patients
decrease neutrophil function- cancer chemotherapy , certain drugs, leukaemia and lymphoma
decreased neutrophil function- chronic granulomatous disease (no respiratory burst) and chediak-higashi syndrome (no phagolysosome formation)