T cells Flashcards

1
Q

T cell antigen recognition

A
  • T cells recognise huge diversity of different antigens
  • each cell expreses a unique T cell receptor
  • TCR is an aB heterodimer or yo heterodimer
  • TCR recognises antigen as complex of antigen peptide fragment with self MHC molecule
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2
Q

T cell receptor structure

A
  • contains a variable region with antigen binding site, constant region, TM region, cytoplasmic tail
  • receptor resembles membrane bound Fab fragment with 3 CDRs per chain
  • one chain equivalent to light and one to the heavy chain of an antibody
  • TCR binds antigen fragment and antigen presenting molecule
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3
Q

TCR diversity

A
  • aB and yo chains of TCR analogous to L and H chains of antibody
  • TCR loci organised in similar way to immunoglobulin genes
  • VJ rearrangement + C segment in a and y chain
  • VDJ rearrangement + C segment in B and o chain (equivalent to heavy chain)
  • same RSS sequence and the 12/23 rule
  • recombinase enzyme catalyzes VJ/VDJ joining
  • no somatic mutation in TCR genes (T cells have no AID)
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4
Q

Why somatic mutation not found in T cellls

A
  • T cells recognise antigen presented on cell surface
  • self reactive T cells dangerous
  • mutation could re-create them
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5
Q

TCR complex

A
  • TCR complex formed of antigen recognition proteins and invariant signal proteins (CD3)
  • cytoplasmic TCR tail too short for signalling
  • TCR signalling by clustering with CD3 and recruiting protein kinases to CD3 cytoplasmic tails
  • CD3 is three dimers associated with recognition
  • CD3 has ITAM sequences for docking of tyrosine kinases
  • complementary charged residues between TCR and CD3 allow association
  • TCR sends signals leading to different outcomes
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6
Q

CD4/8 coreceptors

A
  • T cells express one or the other (2 groups)
  • CD4 has 4 Ig-like domains
  • CD8 has a and B chains (heterodimer) each with 1 Ig-like domain
  • CD4/8 bind to MHC molecules that present antigen to the T cell
  • this helps the T cell to bind to the antigen presenting MHC and target it to specific cell types
  • CD4 recognises MHC class 2 and CD8 class 1
  • MHC presents antigen to the TCR
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7
Q

CD8

A
  • cytotoxic T cells

- MHC 1 found in all cells

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8
Q

CD4

A
  • helper T cells

- class 2 found in APCs

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9
Q

T cell effectors

A
  • contact other cells and induce change
  • CD8 T cells recognise viral infection and kill it
  • CD4 T cells contact macrophage, B cells, induce further response by cytokine secretion
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10
Q

T cell Activation

A
  • need antigen signal and co-stimulatory signal (protective)
  • costimulatory molecules found on APCs
  • they bind to CD28 on the T cell to activate it and induce IL-2
  • amplification procedure lowers threshold of number of TCRs needed to be cross linked by MHC peptide complex
  • CTLA-4 is inhibitory receptor for B7 molecules
  • without infection APCs do not express costimulatory signal
  • self reactive T cells escape negative selection in thymus are not activated
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11
Q

Immunological Synpase

A
  • at point of contact immunological molecules cluster
  • diffusion in membrane to concentrate into focal points of interaction
  • different protein sets segregated into synapse areas
    eg. c-SMAC: central supramolecular activation complex
    eg. p-SMAC: peripheral supramolecular activation complex
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12
Q

T cell signalling

A
  • clustering of TCR and co-receptor (CD4/8) initiates signalling by stimulating phosphorylation
  • in resting T cell ITAMS of CD3 complex non-phosphorylated
  • MHC binding to TCR leads to phosphorylation
  • tyrosine kinase binds ITAMs and is phosphorylated itself
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13
Q

Effector T cell Activation

A
  • co-stimulatory signals NOT required for effector T cell activation
  • IL-2 is cytokine needed for T cell proliferation
  • IL-2 self-stimulates effector Th or Tc
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14
Q

Helper T cells

A
  • CD4
  • no direct anti-pathogen effects but regulate other immune arms
  • determine type of response by cytokine secretion
  • Th1 cell recognises complex of bacterial peptide with MHC 2 and activates macrophage
  • helper T cell recognises complex of antigenic peptide with MHC 2 to activate B cell
  • classes result from activation and development in different cytokine environments
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15
Q

Cytotoxic T cells

A
  • CD8
  • recognise antigens presented by MHC 1
  • directly kill
  • need IL-2 provided by T helper cells
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16
Q

yo T cells

A
  • 10% of T cells
  • limited TCR repertoire
  • high density in mucosal tissue
  • tissue surveillance for stress/homeostasis
  • recognise non peptide antigens
  • binds antigen presented by non classical MHC
  • cytotoxic
  • most have no CD4/8
17
Q

yo receptor expression

A
  • tissue specific
  • express a receptor useful for dealing with pathogens from that site
  • eg thymus predominantly has the Vo1 gene segment
18
Q

Phosphoantigens

A
  • recognised by Vy9:Vo2 T cells
  • phosphorylated intermediates of isoprenoid biosynthetic pathway (different antigen type) secreted by bacterium
  • presented by CD277 (similar to B7 protein) to the Vy9:Vo2 receptor on T cells
  • yo cell activation
19
Q

CD1

A
  • presents lipid antigens and other hydrophobic antigens
  • CD1: MHC 1 like H chains forming heterodimers with B2-microglobulin
  • CD1 proteins non polymorphic
  • deep hydrophobic groove for binding
  • mycobacterial lipid antigens
  • CD proteins recycle between membrane and vesicle membranes to present lipids to surface
  • aB classes recognise CD1a/b/c
  • yo recognise CD1d