Immunology 2 Flashcards

(18 cards)

1
Q

which specific part of a pathogen do adaptive immune cell receptors (BCR or TCRs) target?

A

the epitopes on the antigen surface

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2
Q

what do BCRs recognise?

A

unprocessed antigens in the fluids:
blood, lymph and interstitial fluid

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3
Q

what do TCRs recognise?

A

antigenic fragments that have been processed and then presented by MHC molecules

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4
Q

true or false, MHC binds self and non self

A

true, but T cells only respond to non-self

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5
Q

how does one HLA gene complex code for so many different epitopes?

A

polymorphism: variation within sequences of genes within the population
polygenism: many genes expresses within an individual (we express 6 diff MHC I and 6 diff MHC II - one of the three from each parent)

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6
Q

what is MHC restriction?

A

A T cell can only recognise its antigen when it is presented by its MHC molecule
- binds antigen-MHC complex, not just antigen

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7
Q

what effect does polymorphism have on the MHC molecule

A
  • differing structures of the MHC molecule (effects T cell binding) and the binding groove (effects antigen binding)
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8
Q

describe MHC class I

A
  • binds peptides made endogenously (inside the cell)
  • bind to CD8+ cells which kill infected cells
  • expressed on all nucleated cells (so not RBCs
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9
Q

describe MHC I structure

A
  • 3 alpha regions and one beta
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10
Q

describe peptide loading for MHC class I

A
  • high error rate in translation targets dysfunctional protein for proteolysis
  • Ubiquitin binds dysfunctional protein, which targets it to the immuno-proteasome
  • proteasome chops up protein
  • protein fragments bind TAP 1 and TAP 2, which hydrolyses ATP and fragments enter the RER. then they bind MHC I and it follows secretory pathway without TAP 1 and 2
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11
Q

what does TAP stand for in TAP 1 and 2?

A

transporter associated with
antigen
processing

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12
Q

describe the immunoproteasome

A

in an inflammatory response the B1,2 and 5 subunits are replaced with immunospecific subunits B1i, B2i etc
- proteins cut to specific lengths for MHC 1

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13
Q

describe unbound MHC in the RER

A

very unstable, so requires chaperones to stabilise and dock MHC close to the TAP complex

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14
Q

how can viruses interefere with antigen presentation?

A
  • can interfere with TAPs so proteins cant enter ER
  • can retain MHC I in RER
  • can force it to the lysosome
  • downregulation of MHC at surface
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15
Q

describe MHC class II

A
  • binds peptides from exogenous proteins (proteins that have to be internalised)
  • only found on specialised cells (APCs and B cells)
  • recognise helper T cells
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16
Q

describe peptide loading for MHC class II

A
  • antigen is endocytosed and brought into the lysosome, where pH dependent unfolding happens
  • the lysosome fuses with the endosome, where MHC II is
  • peptides and MHC II is trafficked to cell surface, not yet bound
  • invariant chain is cleaved into CLIP
  • formation of HLA-DM removes CLIP and peptides bind to MHC II
  • presentation
17
Q

what do invariant chains do?

A

they block the MHC II binding groove to prevent ER peptides from binding.

18
Q

what is cross-presentation?

A

when MHC class I loads an exogenous antigen which is not normal