Innate Immunity Flashcards

1
Q

What is innate immunity?

A

Immunity involving pretty much everything apart form lymphocytes and you have it form birth

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2
Q

Is innate immunity antigen specific? What can it recognise?

A

No, can recognise PAMPs or DAMPs using PRR

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3
Q

Which immune cell is particularly important in parasitic infections?

A

Eosinophils

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4
Q

Which type of infection are eosinophils important in?

A

Parasitic

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5
Q

Which immune cell is particularly important in releasing histamines?

A

Mast cells

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6
Q

Which immune cell is particularly important in lysing infected cells?

A

NK cells

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7
Q

Which two immune cells are most abundant and what %?

A

Macrophages and neutrophils (40-75%)

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8
Q

What do macrophages use to recognise targets?

A

Pattern recognition receptors

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9
Q

What are the three main ways the innate immunity system recognises pathogens?

A

PAMPs, DAMPs and detecting missing self

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10
Q

What type of cell usually detects missing self?

A

Natural killer cells

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11
Q

Which immune cells are first to the site of infection?

A

Neutrophils

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12
Q

What soluble mediators do macrophages disperse?

A

Cytokines

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13
Q

What type of nucleus does a neutrophil have?

A

Multilobed.

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14
Q

What are primary granules of a neutrophil?

A

Sites of the enzymes that will kill phagocytksed pathogens

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15
Q

What are secondary granules of a neutrophil?

A

Predominantly involved n replenishing primary granules and regulating the toxins produced during the lysis of pathogens

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16
Q

What is a phagolysosome?

A

A primary granule fused with a vacuole

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17
Q

What (4) steps does a neutrophil take to fight infection?

A

Move to pathogen, bind pathogen, phagocytose pathogen, and kill pathogen

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18
Q

What changes integrin to a high affinity binding state?

A

Chemokine receptor activation on the neutrophil

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19
Q

What helps the neutrophil roll along the surface of cells?

A

Low affinity binding of selectin

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20
Q

What is diapedesis?

A

Movement of a cell across the endothelial layer

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21
Q

What are the two main opsonins?

A

Antibodies and complement proteins

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22
Q

What is opsonisation?

A

Coating of a pathogen with proteins to facilitate phagocytosis

23
Q

Whats the difference in antibody and complement binding?

A

Complement binds to the cell surface and antibodies bind to the receptor on the pathogen

24
Q

What are neutrophil extracellular traps (NETs)?

A

• When neutrophils become highly activated they release these nets that help trap extracellular bacteria and immobilise them

25
Q

Which are bigger, macrophages or monocytes?

A

Macrophages

26
Q

What type of receptors do macrophages/monocytes?

27
Q

What do cytokines do? Where are they released from?

A

Macrophages and they recruit other cells and activate subsequent adaptive immune responses

28
Q

Why do cytokines have to be regulated strongly?

A

They have strong effects at low concentrations

29
Q

What are the 5 types of cytokines?

A

Interleukins, interferons, chemokine, growth factor and cytotoxic

30
Q

What do interferons do?

A

Anti-viral (replication) effects

31
Q

What do interleukins do?

A

Messaging between leukocytes

32
Q

What do chemokines do?

A

Chemotaxis and movement

33
Q

What do growth factors do?

A

all cells of the immune system come from stem cells in the bone marrow, exposure to different growth factors which are a type of cytokine determines what the stem cell becomes

34
Q

What type of pattern do dendritic cells recognise?

35
Q

What do dendritic cells secrete once activated?

36
Q

Do complements need antibodies?

A

Yes, induces lysis of cell. Antibodies induce agglutination

37
Q

Where are components of the compliment system mainly produced?

A

Liver, but also by monocytes and macrophages

38
Q

What does the compliment system have a enzyme cascade system?

A

So that a small initial response can be rapidly amplified

39
Q

When the initial precursor is activated what happens? Explain the enzyme cascade system

A

Initial precursor becomes an activated enzyme. This catalyses the cleavage of many molecules along the chain. This causes the molecule to become an enzyme which does the same thing to the next molecule in the cascade.

40
Q

What three pathways of activation of the complement system are there? Explain each briefly

A

Classical - conformational change in the antibody when it binds leads to complement activation
Alternative - direct activation by the surface of pathogens themselves
Lectin pathway - lectin is a PRR and binds to carbohydrates only present on pathogens

41
Q

What is the main complement component/opsonin?

A

C3 (active component C3b)

42
Q

What happens when C3 is activated?

A

The membrane attack complex (MAC) is formed

43
Q

What does MAC do?

A

Lyse cells

44
Q

What do the cleaved products of enzyme precursors do?

A

They are pro inflammatory mediators that can activate mast cells

45
Q

Three ways complement is controlled?

A

Components have very short half lives
Complement is diluted in body fluids
There are specific regulatory proteins which help regulate the activity of complement (e.g. CD59 is expressed by many normal cells to make them resistant to complement mediated lysis)

46
Q

What four functions does complement have?

A

Lysis, opsonisation, activation of inflammatory response, clearance of immune complexes

47
Q

What causes mast cell degranulation?

A

Inflammatory fragments binding to receptors on the mast cell

48
Q

What do mast cells secrete? What is the met result of mast cell activation?

A

Histamine. Vasodilation and increased vascular permeability.

49
Q

What do alarm cytokines do?

A

Increase vascular permeability

50
Q

What are anaphylatoxins?

A

Proinflammatory mediators

51
Q

What is the opsonin for monocytes?

A

Mannan-binding lectin

52
Q

Do natural killer cells have antigen specific receptors?

53
Q

What are the two types of cell recognition NK cells have?

A

Induced self (stress patterns of self proteins) and missing self (when a cell becomes infected their MHC expression is down-regulated)