Chapter 11 Flashcards

Immunological memory and vaccination

1
Q

How do plasma cells respond in the secondary immunity?

A
  • long-lived plasma cells
    • maintained by bone-marrow stromal cells and IL-6
    • produce highly specific antibodies
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2
Q

How do responses of B cells differ in early primary, late primary and secondary responses?

A
  • early
    • B cells activated by binding to antigen
    • becomes plasma cell
  • late
    • naive B cell binds IgG coated pathogen
    • receives negative signal from inhibitory Fc receptor
    • apoptosis
  • secondary
    • memory B cell binds pathogen
    • activated to become plasma cell
    • produces high affinity antibodies
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3
Q

How is hemolytic anemia prevent in newborns?

A
  • mother infused with anti-RhD IgG antibodies, RhoGAM -> coats fetal RBC
  • no detection by naive B cells
    • instead binding to inhibitory Fc receptor on B cells
  • infused second time after birth
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4
Q

How do memory T cells emerge?

A
  • from naive T cells
    • when binds to DCs -> mitosis
    • produces 2 cells (proximal = closer to DC and distal=further)
      • proximal gets more CD8 and metabolism is started to become effector cell
      • distal has slower metabolism, develops later in the primary immune response
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5
Q

What are the two subpopulations of memory T cells?

A
  • central memory T cells
    • L-selectin and CCR7 produced -> enter secondary lymphoid tissues
    • easily activated, produce IL-2
    • differentiate into effector T cells
  • effector memory T cells
    • no L-selectin and CCR7
    • CCR6, CCR4, CXCR3, CCR5 -> enter non-lymphoid tissues, instead inflamed tissues
    • respond immediately
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6
Q

What are resident memory T cells?

A
  • tissue repair after infection -> memory T cells incorporated
    • fast response
  • most numerous type of memory T cell
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7
Q

What are the types of viral vaccines?

A
  • killed (inactivated) virus vaccines
    • cannot replicate
  • live-attenuated virus vaccines
    • mutant, not pathogenic, grows poorly in humans
    • better for vaccines -> capacity to infect (although small)
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8
Q

What is a subunit vaccine?

A
  • only surface protein purified from plasma membrane of people infected with the virus (ex. HBV)
  • now gene encoding surface antigen of virus inserted into genome of yeast -> surface protein collected
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9
Q

What are types of bacterial vaccines?

A
  • toxic proteins (secreted by bacteria)
    • antibodies bind and neutralise them
    • for vaccine treated with formalin to destroy toxicity, inactivated proteins = toxoids
  • live-attenuated bacteria
  • capsular polysaccharides
    • some bacteria are in capsules -> specific for their species
    • prevents complement activation, can only be opsonised when ab are bound
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10
Q

What are the adjuvants and their role?

A
  • activate innate immunity -> inflammation
    • necessary for adaptive immunity
  • source of antigens to stimulate adaptive immune response
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10
Q

What are conjugate vaccines?

A
  • contain epitopes recognised by B cells and T cells
    • synthetically linked
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