3 Humoral Immunity Part 1 Flashcards

1
Q

Alright I know some cards are long…

A

But I spent a lot of time integrating concepts scattered across different slides to make comparisons simple, so that is why.

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2
Q

T/F Only a few B cells are normally present in the periphery that can bind any 1 antigen?

A

True

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3
Q

T/F a mature B cell requires a costimulatory signal in addition to BCR engagement when it finds its antigen?

A

True

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4
Q

What molecules are expressed on B-1a cells?

A

IgM high
IgD lo
CD11b
CD5

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5
Q

What molecules are expressed on B-1b cells?

A

IgM high
IgD lo
CD11b

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6
Q

What molecules are expressed on B-2 MZ (marginal zone) cells? Where are these cells found?

A

IgM high
IgD lo
-Spleen white pulp marginal zones

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7
Q

What molecules are expressed on B-2 FO (follicular) cells? Where are these cells found?

A

IgM lo
IgD high
CD23
-All peripheral lymphoid organs, esp follicles of spleen and lymph node

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8
Q

Where are both types of B-1 cells typically found?

A

lung pleura and peritoneal cavity (just outside GALT & BALT) and tiny bit in spleen, lymph nodes

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9
Q

What kind of antigens do both types of B-1 cells recognize?

A

Macromolecules usually produced by microbes esp in cell walls:

  • Polysaccharides
  • Phospholipids
  • Self-antigens like phospholipid/cell membrane proteins
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10
Q

What is the reason for why B-1 cells only recognize certain types of antigens?

A

B-1 cells contain only a restricted set of the V(heavy chain) gene segments

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11
Q

What types of B cell is known to be a constant source of “natural” IgM antibodies? Which are an immediate source of IgM’s (within hours) of specific IgM’s? What do these IgM’s do?

A
  • B-1
  • MZ B-2’s
  • Pool of ready-to-use antibodies for early stages of infection
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12
Q

IgM’s are biased to attack what?

A

Microbial products like cell walls (like the B-1 cells that produced them!)

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13
Q

Where are B-2 cells produced? Where do they mature?

A
  • In fetal liver and in bone marrow

- In spleen

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14
Q

Which B cell type is responsible for young childrens’ susceptibility to encapsulated bacteria? What do their antibodies target?

A
  • MZ B-2 cells (these don’t appear until AFTER birth)

- Microbial products (like B-1 cells)

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15
Q

Which B cell types are abundant? Which are few?

A

Very abundant: FO B’2s
Low abundance: All B-1’s
Few: MZ B-2’s

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16
Q

T/F The B-1 progenitor and B-2 progenitor cell are the same?

A

False (Hematopoietic Stem Cell is their earliest common progenitor)

17
Q

When in our lifetime are B’1s produced? How about FO B-2’s and MZ B-2’s?

A
  • Mostly fetus/neonate, but persist and self-renew in adult. Also a few are still made from scratch in adult.
  • FO B-2’s during fetus/neonate, then generated continuously throughout adulthood
  • MZ B-2’s begin production AFTER birth
18
Q

Of the 4 kinds of B cell, which produces highly diverse antibodies?

A

FO

19
Q

Which B cell type is responsible for young childrens’ susceptibility to encapsulated bacteria? What do their antibodies target?

A
  • MZ B-2 cells (these don’t appear for a while after birth)

- Microbial products (like B-1 cells)

20
Q

Each mature B cell (in the periphery) expresses how many types of antibody?

A

1 (and only 1 antigen specificity)

21
Q

What are the components of the BCR?

A
    • Dif than T cells:
  • Antibody (no signaling)
  • CD79a, CD79b (a.k.a. Ig alpha/beta) are the signaling link
  • Co-receptors CD 81, 19, 21 modify/amplify response
22
Q

What happens to activated FO B cells?

A

Migrate toward border of the CD 4 T cell zones in lymph node

23
Q

MZ B’s main function is?

A

Respond to blood-borne antigens (including those in the red pulp)

24
Q

What is B cell signal 1? What happens w/ this signal alone?

A
  • Engagement of multiple BCR’s

- Death/anergy

25
Q

Name the characteristics of TI (thymus-independent in mice) responses?

A
  • Low magnitude
  • Low affinity Ab’s
  • No memory
  • Early phase and short lived
  • Don’t need CD4’s, so no germinal center response
  • IgM antibodies (with some IgG and IgA and limited class switching)
  • Induced by repetitive structural complexes that activate multiple BCR’s
26
Q

What is B cell signal 3?

A

Cytokines (from CD4’s or activated innate cells)

27
Q

What safeguards against B cells going rogue and producing antibodies?

A

Signal 2 and 3

28
Q

What is special about Type 1 TI antigens? What is our example?

A
  • activate PRR’s like TLR (signal 2)

- LPS (lipopolysaccharide)

29
Q

What is special about Type 2 TI antigens? What is our example?

A
  • Can’t provide signal 2, but can recruit things to provide signal 2
  • Bacterial capsule polysaccharides
30
Q

How old before children generate effective TI responses?

A

2 years (recall requires MZ B-2’s)

31
Q

Which B cells mount TI responses? Why?

A
  • B-1 and MZ B-2’s

- Antibodies for microbial pdt’s, anatomic location, rapid response

32
Q

What 3 ways can Type 1 TI antigens be presented to B cells?

A
  • By the bacteria itself
  • By antigen presenting cell
  • As dead chunks of bacteria floating around
33
Q

What 2 ways can Type 2 TI antigens be presented to B cells?

A
  • Signal 2 is provided by something else like the PRR for LPS
  • Signal 2 is provided by complement (C3b)