Immune memory Flashcards

1
Q

mechanisms of B cell memory recall

A

T dependent and T independent- T dependent is much more effective (CD4+ cell activation)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

where do T and B cells communicate?

A

germinal centres

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what activates naive T cells

A

CD28

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

CD4+ recognise:

A

MHC II complexes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

CD8+ recognise:

A

MHC I peptides

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

example of an immune regulation mechanism which occurs at the synapse

A

size-dependent segregation- more physical space between antibody and target means there is a less strong response

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

examples of features which change depending on the state of an immune cell

A

cell surface molecules, division rates, TCR repertoires

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

tuenover rates at each stage of T cell

A

slow in naive T cells- 50% of pop replenished in 9 months ish
activated- speedy, every 10-12 hours but can do up to every 6
intermediate for memory cells- half of pop in 15-70 days

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

tradeoff in specificity of T cells

A

want to be somewhat specific as some antigens are more protective than others, but also can be good to have broad specificity to reduce escape risks

too many types- competition and ‘pushing out’ of some cells

more clones > better survival of responses, which is necessary for the response to be vaguely useful

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

memory T cell sub-populations

A

effector- tissue and spleen migration routes
central- preferential migration through the lymph nodes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

CD4 vs CD8 memory

A

CD4- more diverse repertoire, gradual decline over time
CD8- large clone sizes, potentially more stable

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

central vs effector memory

A

central lived longer, slower transition to function, more division before differentiation
>essentially, slower but larger effect

effector- short-lived, more rapid transition to function
>fast but smaller effect

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

3 differentiation models

A

linear- naive > effector > differential division

bifurcative- asymmetrical cell division, differentiation from daughter cells

self-renewing- lymphoid cells move to non-lymphoid cells, rather than going through an intermediate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

are memory pools committed or non-committed?

A

some of both- there are biases in secondary responses, probably suggesting some level of commitment in memory cell pools

How well did you know this?
1
Not at all
2
3
4
5
Perfectly