Third line of defence Flashcards

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1
Q

what initiates the third line of defence

A

the presentation of an antigen with MHC II markers

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2
Q

what is the role of dendritic cells/macrophages in the third line of defence

A

they engulf and digest a pathogen, presenting the antigens of the pathogens on their own MHC II markers, they then travel to the lymph node where they encounter T helper cells

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3
Q

T helper cells are aka

A

T lymphocytes, CD4+ cells

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4
Q

when a macrophage/dendritic cell encounters a t helper cell, rarely anything happens, why…

A

T helper cells all have unique T-cell receptorrs on there surface, rarely anyything happens because the macrophage/dendritic cell and t-helper cell dont have matching antigens

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5
Q

what happens when the dendritic cell/macrophage encounters the specific T-helper cells

A

they bind and the t-helper cell becomes avtivated, causes the naive t-cells to undergo colonal selection and cytokines are released

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6
Q

what are the two processes of the third line of defence

A

humoural response annd cell mediated response

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7
Q

cell mediated response

A

uses T cells to target antigens, effective against intracellular pathogens

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8
Q

when a helper t-cell secretes cytokines after binding to the macrophage/dendrites, what does this cause

A

the cytokines stimulates the helper t-cells to unergo clonal expansion - rapid miotic division (all with the have same receptors as original) and differentiation into cytotoxic t-cells and t memory cells

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9
Q

what do the cytotoxic cells do once produced/differentiated

A

they spread throughout the body and identify self cells in the body that have foreugn antigens rgat fit their t-cell receptors, presented on its MHC I marker, they tthen release a death lignand that induces apoptosis in the infected in the cell

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10
Q

humoral immunity

A

effective against extracellular pathogens, neutralising and destroying them

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11
Q

structture of B lymphocytes

A

covered in antibodies (immunoglobulins) and contain MHC II markers

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12
Q

where are B lymphocytes found

A

reside in the lymph nodes in high numbers and travel around the blood strea,

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13
Q

what activates a B lymphocyte

A

comes into contact with a pathogen, dendritic cell/acrophage or free virus particles that have the antigen complementary to the shape of the antigen binding site on its cell receptors

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14
Q

once a b lymphocyte encounters dendritic cell/macrophage or free virus particles that have the antigen complementary to the shape of the antigen binding site on its cell receptors

A

Th b lymohcyte will engulf the pathogen by phagocytosis and present the antigens of the pathogen on its own MHC II markers, b lmphocyte is said to be selected

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15
Q

once the b lymphocyte has been selected

A

the t helper cell with the complementary recpetor to the antigen will recognise the selected b cell and secrete cytokines which cause the b-lymphocyte to undergo clonaal expansion and differentiation, producing b memeory cells and plasma cells

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16
Q

plasmaaa cells

A

differentiated clones of the the selected b lymphocyte, they secrete antibodies into the blood to defend against the specific pathogen, short lived cells

17
Q

b memeory cells

A

used for fast response to future exposure of the same pathogen, long lasting

18
Q

what are the five actions of antibodies

A

neutralisationn, aggultination, immobilisation, opsonisation and activation of complement proteins NAIOC

19
Q

neutralisation

A

block the sites of pathogens tthat are used to attack host cells

20
Q

agglutination

A

can bind with antigens on two seperate pathogens making it easier for phagocytes to recognise the pathogen as forgein and destroy it

21
Q

immobilisation

A

restrict the movement of pathogens around the body through the formation of large antigen-antibody complexes

22
Q

opsonisation

A

bind directly to the surface of the pathogen to make it easier for phagocytosis to take place

23
Q
A
24
Q

what is an antibody

A

a specific form of an immunoglobu;in, a protein found on the surface of a b cell, specific in nature

25
Q

structure of an antibody

A

2 heavy chains in the constant region, 2 light chains apart of both the constat and variable regions and two antiigen binding sites, composed of 4 polypeptide chains

26
Q

what are the five classes of antibody/immunoglobulin

A

IgA, IgD, IgE, IgG and IgM, each serve a different function

27
Q

epitope

A

a localised region on the surface of an antigen that is capable of eliciting an immune response and of combining with s dpecific antibdy to counter that response

28
Q

what occurs in the primary response

A

either by vaccination or natural exposure to an active pathogen/agent, their is a delay in the production of antibodies because of the need for clonal expansion and differentiation

29
Q

when does the secondary response occur

A

immunization booster, re-exposure to active pathogen/agent or a reaction to being exposed to the pathogen again

30
Q

how is the antibody production different in the secondary response on a graph

A

faster immune response and production of antibodies and more antibodies are produced, and they remain for a longer time

31
Q

why is the secondary response result in faster production of antibodies

A

there are many memory cells avaliable to the pathogen/agent, so there is no need for great clonal expansion, only a small amount of differentiation is required for memeory cells to be able to produce large amount of antibodies

32
Q

what is rhesus factor

A

a protein that is either present or absent on the surface of red blood cells

33
Q

if the rhesus factor is present

A

the blood is positive

34
Q

if the rhesus factor is absent

A

the blood is negative

35
Q

what is haemolytic disease

A

can occur in a newborn if there is rhesus incompatibility between the mother and her unborn child, occurs if the mother is negative and the father is positive and a positive baby is produced

36
Q

why is rhesus incompatibility harmful

A

if the positive blood from the baby enters the negative mothers blood stream, it will trigger an immune response as the rhesus protein will be recogniseed as an antigen

37
Q

how is haemuolytic disease treated

A

giving the mother a vaccination containing rhesus antiibodies, this blocks the antigens on the babies red blood cells that have entered the mothers blood stream, preventing an immune response and the build up of memory cells

38
Q
A