CSIM 1.25 - T-cells 2 Flashcards

1
Q

What is Di-George’s syndrome?

A

Hereditary condition in which there is a missing thymus/parathyroid gland, therefore NO T-cell maturation can occur

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2
Q

When does T-cell receptor VDJ recombination occur?

A

When the T-cell progenitors are double-negative - VDJ recombination leads to the formation of CD4 and CD8 receptors (double-positive)

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3
Q

Describe positive T-cell selection within the thymus?

A

Successful T-cell recognition with MHC molecule induces survival signals

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4
Q

Describe negative T-cell selection within the thymus?

A

T-cell is tested against SELF-Ag in the thymus medulla - T-cells which bind avidly with self-Ag are apoptosed (central tolerance)

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5
Q

Which T-cell binds to MHC class 1?

A

CD8 T-cytotoxic cells

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6
Q

Which T-cell binds to MHC class 2?

A

CD4 T-helper cells

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7
Q

Structurally how does Ag recognition by T-cells occur?

A

Ag bound at MHC-cleft of antigen presenting cell and the CDR.3 region of the T-cell receptor binds to the Ag

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8
Q

Where are viral proteins synthesised in host cells and how are they converted into peptide Ag?

A

Cytosol

Proteosomes

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9
Q

Once viral protein is degraded where are the peptide Ag transported and how?

A

Endoplasmic reticulum lumen

TAP 1 and TAP 2 enzymes

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10
Q

Where are MHC class 1 molecules synthesised?

A

Endoplasmic reticulum lumen

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11
Q

How does the Ag end up inside the MHC class 1 molecule cleft?

A

MHC class 1 molecule (synthesised in the ER lumen) binds to TAP enzyme (transporting Ag) and Ag moves into MHC class 1 cleft. This is then transported to the cell surface

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12
Q

Name a pathogen which replicates in endosomes and state why this may be problematic?

A

T.B

Protein is not accessible to proteosomes (cytosol)

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13
Q

What happens as the endosome progresses into the cell interior?

A

Increases in acidity and protein inside endosome is degraded

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14
Q

Where are MHC class 2 molecules synthesised?

A

Endoplasmic reticulum lumen

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15
Q

Which molecule blocks the MHC class 2 cleft following its synthesis and what is its significance?

A

Li - MHC(II)/Li complex transported and fused to the acidified endosome where the Li is degraded and Ag binds to MHC class 2 cleft. This is then transported to the cell surface

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16
Q

Describe polyclonal proliferation and give a clinical example resulting from when this occurs in excess?

A

As APC potentially carry multiple Ag, multiple naive and specific T-cells may be activated
Toxic shock syndrome (acute septicaemia) occurs with activation of >50% of the body’s T-cells

17
Q

How are naive T-cells activated?

A

Specific Ag in conjunction with specific MHC complex

2nd co-stimulatory signal by APC interaction

18
Q

Describe the co-stimulatory signals required to activate T-cells?

A

APC - CD80 (B7.1) and CD86 (B7.2)
T-cell - CD28
Signals up-regulated with danger signals

19
Q

What happens when a naive T-cell recognises its specific Ag and MHC complex and DOES NOT receive a co-stimulatory signal by the APC?

A

The T-cell becomes anergic - unresponsive to further stimulation by the specific Ag (shot it’s gun)

20
Q

What is special about memory T-cells?

A

Do NOT require the 2ndary co-stimulatory signal from the APC to activate