Genetics of antigen receptors Flashcards

1
Q

Where is innate immunity encoded?

A

In the germline- inherited

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2
Q

What are the receptors of innate immunity and what do they recognise?

A

Pattern recognition receptors e.g. TLR. Recognise PAMPS and DAMPS.

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3
Q

How is adaptive immunity generated?

A

Somatically

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4
Q

Example of adaptive immunity receptors.

A

BCRs and TCRs

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5
Q

Explain clonal selection of lymphocytes.

A

Progenitor cells give rise to large numbers of naive circulating lymphocytes, each with a different specificity.
When a lymphocyte recognises an epitope in a dangerous context then this useful clone is expanded to combat the threat.
This also generates memory cells.

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6
Q

What two regions do BCRs and TCRs contain?

A

Complementary determining region and signal transfusing molecules.

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7
Q

What is the effector mechanism of BCR?

A

Recruited by FcR interactions of different soluble antibody isotypes.

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8
Q

What is the effector mechanism of TCR?

A

Mediated by cell-contact or local secretion of cytokines.

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9
Q

What do the highly variable and low variability regions on a Kabat and Wu plot translate to?

A

The loop is a highly variable region which is the antigen binding region on the structure.
The low variability region is the framework which is the complementarity determining region.

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10
Q

What are the two types of light chain?

A

Kappa or Lambda.

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11
Q

How is variability generated in the antigen binding region?

A

Lineage specific, developmentally regulated (series of checkpoints), somatic recombination of multiple gene segments.

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12
Q

What do V and J segments join to become?

A

V exon

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13
Q

Molecularly, how do B cells achieve different antigen binding sites?

A

They choose different V and J segments via gene rearrangement.

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14
Q

How does the heavy chain achieve its diversity?

A

It contains an extra type of gene segment called Diversity.

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15
Q

What is the V exon in a heavy chain composed of?

A

VDJ segments

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16
Q

What do V, D and J all correspond too?

A

Complementarity determining region 3

17
Q

How is diversity increased further?

A

Imprecise joining

18
Q

What are the sources of diversity in the primary antibody repertoire?

A

Combinatorial diversity

Junctional diversity