#5 Antibody-Mediated Immune Response Flashcards

1
Q

Negative selection of B cells

A

If a B cell recognizes self-Ags, then it will undergo RECEPTOR EDITING (Ig gene recombination to make new light chain)

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2
Q

The activation of B cells by Ag in the lymph node does the following:

A

↑ B cell proliferation

↑expression of MHC class 2, B7(CD80/CD86), receptors for cytokines made by Th cells

secrete low level of IgM

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3
Q

Help from Complement

A

CR2 is important in beginning of infection b/c there isn’t much Ag

CR2 binds C3d (a fragment of C3b that’s on the bacteria)→makes B cell very sensitive to Ags

*B cell recognizes Ag labeled by innate immunity

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4
Q

Where do B cells go after activation?

A

Lymphoid follicle → T cell-rich zones of lymph node

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5
Q

B cells are professional APC

A

True

They can engulf and present via MHC class II. This is required in order to have T helper cells activate B cells

(Many different CD4+ cells can activate a single B cell)

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6
Q

How T cells activate B cells

A

Stimulatory signals

CD40L (T helper cell) + CD40 (B cell) → signal sent

If BCRs have been cross-linked, then B cell is activated

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7
Q

B cell Ig Class Switching

A

First activated, B cell makes mostly IgM →can switch to IgG, IgA, IgE

  • Ab class is determined by Fc heavy chain region
  • B cell cuts off IgM constant region DNA and puts on a different one
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8
Q

IgE

A

IgE: Immunity vs helminths, mast cell degranulation

IgA: Mucosal Immunity

IgM: Complement activation

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9
Q

What are the 2 cells that a B cell can become?

A

Plasma cell (Ab factory) or memory cell

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10
Q

Where do plasma cells travel?

A

To spleen or back to bone marrow

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11
Q

How long does plasma cell live for?

A

5 days

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12
Q

B cell → Memory cell

A

CD40-CD40L interaction is critical

*T cell needs to activate B cell in order to make plasma or memory cells

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13
Q

B cells via Thymus-dependent and Independent

A

DEPENDENT: Proteins need help of Th2 cells to stimulate B cells to make Ab and memory cells → Thymus DEPENDENT. Thymus dependent antigens require B cells to have direct contact with T helper cells in order to form antibodies. This is how a typical humoral immune response is carried out in the case of most antigens. An APC presents antigen to a T helper cell, the T helper cells can then present antigen to the B cell and it is activated to produce antibodies.

INDEPENDENT: Chemical nature: polymeric antigens (polysaccharides, glycolipids, nucleic acids) (2nd signal via Toll-like receptors)type 1) or B cell receptor clustering(type 2))

Thymus independent antigens activate B cells by other mechanisms. They can be bacterial cell wall components, like lipopolysaccharides. These are called TI-1 Antigens. Or they can be highly repetitious molecules, like the proteins that make up bacterial flagella. These are TI2-Antigens.

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14
Q

What are the 2 types of TI Ags? (thymus independent)

A

TI-1 Ags are polyclonal activators of B cells

TI-2 Ags (not polyclonal) are Ags with repeating epitopes for cross-linking BCRs

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15
Q

TI-2 Ags

A

-Generated against repetitive Ags, direct BCR cross-linking, mostly IgM, low affinity, no memory

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16
Q

Clinical Significance of TI Ags

A
  • Many bacterial cell wall polysaccharides (pneumococcus, meningococcus, Haemophilus) come from TI Ags
  • Ab-mediated immunity against encapsulated bacteria (B cells can be activated right away and not have to wait for T cells)
  • Patients with congenital or acquired deficiencies of Ab-mediated response → susceptible to infections with encapsulated bacteria