Immunological Memory & Vaccines Flashcards
Three kinds of B cells generated during an original activation by an antigen
- short-lived plasma B cell
- long-lived plasma B cell
- central memory B cell
central memory B cells take up residence in the …
lymphoid organs
where do long-lived plasma B cells reside in?
take up residence in bone marrow
which cells resupply the long-lived plasma B cells
central memory B cells
Two main kinds of T cells generated during original activation by an antigen
- memory effector T cells
2. central memory T cells
which memory T cell resides in the secondary lymphoid organs?
central memory T cell
which memory T cell circulates in the bloodstream and is in the tissues?
memory effector T cells
Three main properties of adaptive memory responses
- memory response to a second attack is much faster and more robust bc there are more cells to respond than during the initial activation
- memory B and T cells are easier to activate bc they’ve already gone through the ‘two-key’ selective stimulation process and are ‘ready-to-go’
- with memory b cells, the response has also been refined by class switching and affinity maturation
T or F. B cells continue to deploy their weapons (Abs) even after an invasion is stopped, whereas T cells do not
T
How do we know what type of immunity we need?
- examine people who survive an infection
- see what response they’ve made to what part of the organism, and determine if we can use that information to our advantage
non-infectious vaccines use …
Th and B cell memory only
list non-infectious vaccines
- killed whole organisms
- parts of organisms = usually requires boosters to obtain and maintain full immunity
glycanp-peptides
endosomal degradation of glycoconjugates yields processed glycans conjugated to peptides
glycoconjugate vaccines
glycanp-peptides not peptide-only components that are presented on MHC II molecules
- the peptide component binds to the MHC II molecule, while the covalently attached glycanp component is recognized by the T-cell receptor
These vaccines can stimulate CTL memory
attenuated vaccines
properties of attenuated vaccines
- live and infectious but NOT virulent
- vaccines for viruses typically (mutated so can’t cause full-blown disease)
- infection of APCs provides basis for CTL memory
- produces better local immunity, more like natural infection
- immunity lasts longer with fewer or no boosters needed
- can mutate and revert to virulence but rarely
Carrier vaccines
- novel
- “trojan horse strategy”
- uses non-pathogenic virus engineered to carry some key genes of a pathogen
- can produce memory CTLs
RNA vaccines
- novel
- DCs take up mRNA, translate it to produce proteins that are then presented to B and T cells
- can produce memory CTLs
Logic for vaccine adjuvants
- good immune response requires that vaccines be seen as both foreign and dangerous
- both signals occur with attenuated vaccines
- non-living vaccines only seen as foreign SO…
- adjuvants (like aluminium hydroxide or MPL) provide a danger signal to improve the immune response to protein or other non-living component vaccines