Immunological Memory & Vaccines Flashcards

1
Q

Three kinds of B cells generated during an original activation by an antigen

A
  1. short-lived plasma B cell
  2. long-lived plasma B cell
  3. central memory B cell
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2
Q

central memory B cells take up residence in the …

A

lymphoid organs

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3
Q

where do long-lived plasma B cells reside in?

A

take up residence in bone marrow

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4
Q

which cells resupply the long-lived plasma B cells

A

central memory B cells

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5
Q

Two main kinds of T cells generated during original activation by an antigen

A
  1. memory effector T cells

2. central memory T cells

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6
Q

which memory T cell resides in the secondary lymphoid organs?

A

central memory T cell

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7
Q

which memory T cell circulates in the bloodstream and is in the tissues?

A

memory effector T cells

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8
Q

Three main properties of adaptive memory responses

A
  1. memory response to a second attack is much faster and more robust bc there are more cells to respond than during the initial activation
  2. 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’
  3. with memory b cells, the response has also been refined by class switching and affinity maturation
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9
Q

T or F. B cells continue to deploy their weapons (Abs) even after an invasion is stopped, whereas T cells do not

A

T

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10
Q

How do we know what type of immunity we need?

A
  • 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
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11
Q

non-infectious vaccines use …

A

Th and B cell memory only

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12
Q

list non-infectious vaccines

A
  • killed whole organisms

- parts of organisms = usually requires boosters to obtain and maintain full immunity

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13
Q

glycanp-peptides

A

endosomal degradation of glycoconjugates yields processed glycans conjugated to peptides

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14
Q

glycoconjugate vaccines

A

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

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15
Q

These vaccines can stimulate CTL memory

A

attenuated vaccines

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16
Q

properties of attenuated vaccines

A
  • 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
17
Q

Carrier vaccines

A
  • novel
  • “trojan horse strategy”
  • uses non-pathogenic virus engineered to carry some key genes of a pathogen
  • can produce memory CTLs
18
Q

RNA vaccines

A
  • novel
  • DCs take up mRNA, translate it to produce proteins that are then presented to B and T cells
  • can produce memory CTLs
19
Q

Logic for vaccine adjuvants

A
  • 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