Lecture 30 Flashcards

1
Q

what part of the omicron spike protein is mutated to evade the immune system?

A

N-terminal domain and receptor-binding domain

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2
Q

hematopoietic tree

A

starting in BM, immune cells derive from hematopoeitic stem cell

then split into common lymphoid progenitor (adaptive) or common myeloid progenitor (innate)

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3
Q

humoral vs cellular immunity

A

humoral = B cells producing Ab
cellular = T cells bind Ag

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4
Q

development of humoral immunity

A
  1. lymphocytes originate from stem cells in BM
  2. B cells mature in BM
  3. B cells encounter Ag and mature into plasma cells that make Ab
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5
Q

development of cellular immunity

A
  1. lymphocytes originate from stem cells in BM
  2. T cells mature in thymus and enter circulation
  3. T cells use TCR to fight infection
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6
Q

clonal selection of B cell

A

B cell binds its antigen to cause B cell division

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7
Q

clonal expansion of selected B cell

A

B cell division = proliferation –> primary immune response

creates 1st wave: Ab-secreting plasma cells and memory cells that stay in circulation

2nd wave: if antigen encountered again

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8
Q

3 types of active agents of a vaccine

A
  1. inactivated
  2. attenuated
  3. purified components of pathogen
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9
Q

what does a successful vaccine rely on? why?

A

memory!

vaccine induces the primary immune response and generates memory cells that are active when the infection occurs

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10
Q

why are next generation vaccines better?

A

ex. RNA vaccine –> uses host cells to produce antigen which is much faster

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11
Q

how many types of light chains are there? what are they?

A

2: kappa and lambda

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12
Q

gene segments of light chains

A

V, J, and C

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13
Q

2 possible light chains

A

kappa/kappa OR lambda/lambda

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14
Q

how many types of heavy chains are there? what are they?

A

5: alpha, delta, gamma, epsilon, or mu

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15
Q

gene segments of heavy chains

A

V, D, J, and C

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16
Q

how many Ab can be produced with different specificities?

A

10^11

17
Q

3 ways of generating Ab diversity?

A
  1. somatic recombination
  2. junctional diversity
  3. somatic hypermutation
18
Q

describe somatic recombination of light chain (DNA –> pre-mRNA –> mature mRNA)

A
  1. RAG1/2 cuts at 3’ end of a variable region and 5’ end of a joining region to join random V and J segments (at level of DNA)
  2. transcription begins at the selected V region to make pre-mRNA with joint V and J and other J regions
  3. pre-mRNA is spliced to remove remaining J regions and mature mRNA with only 1 V, J, and C region is transplated
19
Q

does a B cell always make the same Ab? why?

A

yes

because somatic recombination occurs at the DNA level

20
Q

how much of Ab diversity is due to somatic recombination?

A

4.5x10^6

21
Q

which Ab segment does NOT contribute to Ab specificity?

A

constant region

22
Q

what is junctional diversity?

A

a few random nucleotides are lost or gained (may lead to frameshift that produces nonfunctional gene)

23
Q

what is somatic hypermutation?

A

immunoglobulin genes have high mutation rate

24
Q

example of point mutation created in somatic hypermutation

A

cytosine deaminated to uracil –> DNA repair mechanisms replace the uracil with another base to make a point mutation

25
Q

2 chains of TCR?

A
  1. alpha
  2. beta
26
Q

what gene segments are in the alpha chain?

A

V, J, C

27
Q

what gene segments are in the beta chain?

A

V, J, D, C

28
Q

what are the mechanisms for generating TCR diversity?

A

somatic recombination and junction diversity