Immune memory Flashcards
mechanisms of B cell memory recall
T dependent and T independent- T dependent is much more effective (CD4+ cell activation)
where do T and B cells communicate?
germinal centres
what activates naive T cells
CD28
CD4+ recognise:
MHC II complexes
CD8+ recognise:
MHC I peptides
example of an immune regulation mechanism which occurs at the synapse
size-dependent segregation- more physical space between antibody and target means there is a less strong response
examples of features which change depending on the state of an immune cell
cell surface molecules, division rates, TCR repertoires
tuenover rates at each stage of T cell
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
tradeoff in specificity of T cells
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
memory T cell sub-populations
effector- tissue and spleen migration routes
central- preferential migration through the lymph nodes
CD4 vs CD8 memory
CD4- more diverse repertoire, gradual decline over time
CD8- large clone sizes, potentially more stable
central vs effector memory
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
3 differentiation models
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
are memory pools committed or non-committed?
some of both- there are biases in secondary responses, probably suggesting some level of commitment in memory cell pools