Cell Mediated Immunity Flashcards

1
Q

Describe an immature dendritic cell

A

Main function is to CAPTURE antigen; high levels of receptors, low levels of MHC and co-stimulatory molecules.

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2
Q

Describe a mature dendritic cell.

A

Main function is to PRESENT antigen; Opposite receptor and molecule expression than immature dendritic cell.

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3
Q

What does a newly activated T cell secrete?

A

IL-2 and express high affinity IL-2 receptor. The low affinity receptor is expressed on naive T cells.

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4
Q

Describe the composition of the Low affinity receptor.

A

Dimer of beta and gamma chain

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5
Q

Describe the composition of the high affinity receptor.

A

Trimer of beta, gamma and alpha chain; Always expressed on regulatory T cells.

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6
Q

What are the fates of cells in clonal expansion?

A

They will either become effector cells or memory cells.

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7
Q

What is the role of chemokines and chemokine receptors?

A

Changes in chemokine receptors and adhesion molecules allow newly activated T cells to exit lymph nodes or spleen, enter the blood circulation and move to the site of inflammation.

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8
Q

How does a dendritic cell control T cell differentiation?

A

The immunological synapse between a professional APC and Th0 cell. The cytokines released determine the type of T cell.

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9
Q

What determines which cytokines are produced by a dendritic cell or other APC while interacting with a Th0?

A
  1. Host genetics
  2. Type of infection
  3. Type of TLR engaged on the APC
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10
Q

Understand the type of signal chart and picture

A

Pg 76

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11
Q

Which cytokine makes a Th0 differentiate into a Th1 cell?

A

IL-12; Happens during an intracellular infection. IL-18 promotes a Th1 response by amplifying the effects of IL-12. Both IL-12 and 18 help activate NK cells.

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12
Q

Which cytokine makes a Th0 differentiate into a Th2 cell?

A

IL-4; Happens during an extracellular infection. Mast cells and basophils make IL-4.

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13
Q

Which cytokine makes a Th0 differentiate into a Th17 cell?

A

IL-23; TGF-B and IL-6 in their differentiation. Response to extracellular bacteria and fungi. Made by dendritic cells and macrophages.

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14
Q

Which cytokine makes a Th0 differentiate into a Treg?

A

IL-10/TGF-F; Must be in the absence of IL-6.

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15
Q

Which cytokine does Th1 cells secrete?

A

They secrete IFN-y and IL-2 which stimulates clonal expansion.

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16
Q

What are the effects of IFN-y secretion?

A
  1. Activates macrophages
  2. Upregulates MHC 1 and 2 on APCs and endothelium.
  3. Inhibits development of Th2 and Th17.
  4. Activates isotype switching in B cells to make IgG
17
Q

Describe the positive feedback cycle between macrophages and Th1 cells.

A

IFN-y activated macrophages make IL-12, which promotes Th1 cell development. Th1 cells then secrete IFN-y; Delay type hypersensitivity.

18
Q

What does Th2 cells secrete?

A

IL-4, 21,5,6,10 and 13.

19
Q

What does IL-4 do?

A
  1. Induce Th0 into Th2
  2. Suppresses inflammatory function of macrophages
  3. In conjunction with with IL-21,5 and 6, it promotes proliferation of B cells and isotype switching to IgG and IgM
  4. In conjunction with IL-13 it promotes isotype switching to IgE and wound healing by alternative macrophages.
20
Q

What does IL-13 do?

A

Stimulates mast cell proliferation

21
Q

What does IL-10 do?

A

Surpresses Th1 response.

22
Q

Which cells make IL-17?

A

Th17 cells;

  1. Stimulates changes in vessels that increase chemotaxis of neutrophils, especially in skin and mucosa.
  2. Defense against extracellular bacteria and parasites.
  3. Inhibited by Th1 or Th2 response
23
Q

Know chart on pg 84

A

see coursepack

24
Q

How do CD8s stop an intracellular pathogen?

A

Does not require co-stimulation through CD28/B7 interaction; Induces apoptosis.

  1. Cytotoxic granules containing perforin and granzymes.
  2. Fas ligand on CD8 binds to Fas receptor on target cell.
  3. CD8s secrete IFN-y which activates macrophages to phagocytose infected cells.
25
Q

What are the two mechanisms of controlling T cell responses?

A
  1. Lack of stimulatory signals
  2. Inhibitory receptors
  3. Death receptors