Introduction Flashcards

1
Q

do all animals have immune systems

A

yes, even primitive ones like sponges have phagocytes

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2
Q

phagocytes

A

innate- look foreigners and engulf

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3
Q

only after shark species had evolved did

A

B and T cells start playing a role in immunity

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4
Q

snails are

A

major vectors of human parasites

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5
Q

humans have

A

highly diverse TLRs (TLR expansion)

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6
Q

primitive fish

A

have components which look like antibodies

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7
Q

as the immune system gets more complex

A

huge expansion and variability of T and B cells

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8
Q

humans have good

A

adaptive memory due to memory cells

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9
Q

Mab 5C04 (4)

A
  • grows quickly
  • produces lots of antibodies
  • v robust
  • do not need extra supplementation to grow well
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10
Q

adaptive immunity has become

A

increasingly efficient in vertebrates

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11
Q

how many cells in immune system

A

10^12

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12
Q

how many cell in brain

A

10^11

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13
Q

number of cell types in immune system

A

> 10

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14
Q

how many cells in brain

A

2

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15
Q

how man connections in immune system

A

infinite

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16
Q

why is the immune system described as being in a constant arms race with pathogens

A

as pathogens adapt and changes, so does the immune system

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17
Q

immunity become much more sophisticated

A

when the thymus and spleen had developed in the body

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18
Q

thymus

A

Main organ of lymphatic system.

  • key to adaptive immunity
  • nursury for maturation of T-lymphocytes
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19
Q

T-lymphocytes

A

mature in te thymus and then leave and are transported via blood vessels to the lymph nodes and speed.

–> cell-mediated immunity- activation of certain immune cells to fightt infection

20
Q

Lymphatic organs

A

thymus and spleen

21
Q

spleen

A

Largest organ or lymphatic system.

  • Its primary function is to filter blood of damaged cells, cellular debris, and pathogens
  • maturation of lymphocytes
  • The spleen also contains efferent lymphatic vessels, which transport lymph away from the spleen and toward lymph nodes.
22
Q

dendritic cells

A

relay innate immunity to the adaptive immune system

23
Q

GALT

A

gut-assosicated lymphoid tissue

24
Q

what is GALT?

A

is a component of the mucosa-associated lymphoid tissue (MALT) which works in the immune system to protect the body from invasion in the gut.

25
Q

70% of immune system is

A

dedicated to the gut

26
Q

why is 70% of the immune system dedicated to the gut

A

mouth is vulnerable entry into the body
o food is potentially very damaging
o gut has to be able to discriminate
 e.g. spicy curry- stomach inflammation
 distinction between pathogen trying to access blood stream and normal food

27
Q

immune system is situated in

A

lymphatic and lymph organs

28
Q

circulation of plasma and WBCs through interstitial space/tissues and back via lymphatics to lymph nodes allows

A

surveillance of tissues for foreign molecules and pathogens

29
Q

LPS is

A

a potent activator of immunity

30
Q

B-lymphocytes express

A

antibodies as B cell receptors

31
Q

T-lymphocytes express

A

T cells receptors

32
Q

during the adaptive immune response

A

B- and T-lymphocytes with receptors specific for particular pthogen molecules proliferate.

33
Q

what forms the basis of protective immunity and immunological memory

A

clonal selection and expansion- protects the body be protected from future attacks

34
Q

innate response comes first and involves

A

phagocytes
inflammatory cytokines
interferon-antiviral
cytokines

35
Q

adaptive response involves

A

T cells
Antibodies
Cytokines

36
Q

when does adaptive response start

A

day 6 after infection

37
Q

example of how infection causes inflammation and swelling

A

1) bacteria trigger macrohages to release cytokines and chemokine
2) vasodilation and increased vascular permeability cases redness, heat and swelling
3) inflammatory cell migrate into tissue, releasing inflammatory mediators that cause pain

38
Q

why does molecular and cellular interactions antigen recognition, cell signalling, cytokines and chemokine.. not lead to chaos….

A

But it doesn’t because the immune system has evolved to be a complex but very robust system that maintains homeostasis while at the same time being able to rapidly commit to particular courses of effector action to counter disease threats.

39
Q

pathogens have

A

their own molecular signatures (antigens) known as PAMPs

40
Q

pathogen recognition

A

Immune cells have invariant receptors on their surfaces known as PRRs that recongise many PAMPs.

Once a pathogen is recognised, a cascade of events occur- activating immune response to destroy it.

41
Q

innate immunity

A

Binding of PAMPs by PRRs on phagocytic cells (e.g. macrophages in peripheral tissues) leads to an innate immune response.
 FAST
 requires no immunological memory

42
Q

adaptive immunity

A

This response is slower and activated by a cascade of chemical signals form sites of infection, and physically interaction with Phagocytic cells of the innate immune system know as DENDRITIC CELLS that migrate from sites of infection into lymphatic system to activate LYMPHOCYTES.§

43
Q

the extent to which the immune system are activated depends on

A

severity, context and

duration of disease - innate immunity is usually all that’s needed for a minor cut or splinter for example.

44
Q

composition of RBC

A

44%

45
Q

composition of WBC

A

1%

46
Q

composition of Plasma

A

55%

47
Q

serum

A

plasma without clotting factor