6. B-lymphocytes Flashcards

1
Q

Where does rearrangement take place?

A

In the bone marrow

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2
Q

What Ig does the immature B-cell express

A

IgM

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3
Q

The mature B-cell leaving the bone marrow expresses.. on its surface

A

IgG and IgM

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4
Q

Negative selection process in the bone marrow

A

Some B cells express receptors that are autoreactive. These will be eliminated

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5
Q

Where does B cells become activated?

A

In secondary lymphoid organs

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6
Q

Receptor editing

A

If maternal BCR is expressed but recognizes self, cell can silence that gene and express paternal alllele instead

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7
Q

Follicular B2 cells

A
  • Develop in secondary lymphoid organs
  • Always need a T helper cell for full activation (TD-response)
  • Usually protein antigens
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8
Q

Marginal zone B2 cells

A
  • Don’t make it to follicle, stay in marginal zone in spleen
  • Can mature without help of T helper cells (TI response)
  • Usually non-protein antigens
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9
Q

B1 B cells

A
  • Non protein antigens (polysaccharides, lipids etc.)

- TI response

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10
Q

What initially happens in the paracortical areas of the lymph nodes?

A
  • T cells come into contact with DCs that carry antigen ->DC present antigen and costimulate the T cells found in the lymph node -> T cells differentiate into Th1, Th2, Th17
  • B cells starts interacting with antigens -> starts migrating to paracortex
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11
Q

Activation of B cell in paracortex

A
  • IgM and IgG receptors cross link
  • B cell with antigen from environment will present this on its surface -> If it can interact with Th2 cell -> further activation
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12
Q

What happens to the B cells after they’re activated in the paracortex?

A
  • Some can mature immediately to become transient plasma cells -> extrafollicular region
  • Some become follicular B cells influenced by follicular T helper cells
  • Some migrate to cortex of the lymph node, where T cells secrete cytokines for further maturation of B cells (non plasma cell)
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13
Q

Affinity maturation

A
  • Mutations occur during VDJ recombination -> some receptors will be weaker, others will be stronger
  • Help from follicular DCs that will present antigens to the developing B cells to see if they bind more strongly or weakly
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14
Q

Isotype switch/class switch

A
  • IFNgamma rich area -> will produce IgG
  • IL-5 rich area -> IgA produced
  • IL-4 / IL-13 -> IgE produced
  • If no change in area, IgM will be produced
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15
Q

IgA

A
  • Dimer

- Produced by plasma cells situated under mucosal surfaces

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16
Q

IgG

A
  • Most important opsonization Ab
  • Mediates the antibody-dependent cellular cytotoxicity (ADCC)
  • Can cross the placenta
17
Q

IgE

A
  • Helps with ADCC action via eosinophils

- Activation of mast cells

18
Q

CD32

A

Feedback inhibition of B cells

Fc gamma receptor

19
Q

Localization of B-memory cells

A

Mantle zone

20
Q

Passive immunization of infants

A

Through breast milk with IgA

21
Q

Passive immunization of fetus

A

Transplacental transport with IgG