IMMUN: Adaptive Immunity Flashcards

1
Q

epitope

A
  • part of the antigen that binds to the antibody
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2
Q

how do B and T cells recognise pathogens

A
  • B cells: have antibodies (4 chains) on surface - IgD and IgM
  • T cells: T cell receptors (2 chains, a and B) and co-receptors (CD4/CD8)
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3
Q

2 diff types of T cells

A
  • T helper cell: has CD4 co-receptor, binds to MHC II molecules
  • cytotoxic T cell: has CD8 co-receptor, binds to MHC I molecules
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4
Q

what signals do Th cells need to be activated

A
  • need 3 signals, only a dendritic cell can provide all 3
  • 1) peptide:MHC
  • 2) co-stimulation
  • 3) cytokines
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5
Q

how do dendritic cells activate T cells

A
  • when patrolling body - good phagocytes, bad APCs
  • if recognise pathogen - bad phagocytes, good APCs b/c upregulate costimulatory molecules (signal 2), then presents antigen on MHC II marker (signal 1)
  • specific type of PAMP drives production of pro-inflammatory cytokines
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6
Q

3 similarities between MHC I and MHC II markers

A
  • transmembrane domains (cross plasma membrane)
  • non-variable region: MHC I binds to CD8 (Tc) and MHC II binds to CD4 (Th)
  • peptide-binding cleft (antigen binding site): many antigens can fit but only one can bind
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7
Q

2 types of MHC markers

A
  • MHC I (only a chain): on all nucleated cells b/c cytotoxic T cells need to be able to kill any virally infected cell, present endogenous material
  • MHC II (a + B chain): subset of cells e.g. dendritic cells, macrophages, B cells etc, present exogenous material from engulfed pathogens
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8
Q

MHC II pathway

A
  • extracellular pathogen is recognised, engulfed and destroyed by phagocyte
  • MHC II marker produced in the RER and joins with non-self antigen in a vesicle
  • peptide/MHC II complex transported to cell surface and expressed
  • recognised by CD4 Th cells
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9
Q

MHC I pathway

A
  • intracellular pathogen is moved to cytosol
  • pathogen tagged w/ ubiquitin and cleaved in proteasome
  • peptide moved into RER for loading onto MHC I markers (finds the one that can bind the strongest)
  • peptide/MHC I complex transported to cell surface and expressed
  • recognised by CD8 Tc cells
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10
Q

3 characteristics of MHC markers

A
  • co-dominant: MHC alleles from both parents are expressed > diversity in population
  • polygenic: multiple genes contribute to building the MHC marker
  • polymorphic: multiple alleles/variations of the MHC genes > diversity in the peptide binding cleft b/n diff ppl > allows any pathogen to be processed and presented
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11
Q

antibody structure

A
  • Y-shaped structure with 2 antigen binding sites
  • mirror image
  • variable (antigen binding site) and non-variable regions
  • heavy and light chains
  • Fab (fragment of antibody binding) and Fc (fragment crystallisation) regions
  • 2 arms can hinge (Fab section)
  • transmembrane region (crosses plasma membrane)
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12
Q

lineage of T cells

A
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13
Q

how do CD4 (Th) cells activate CD8 (Tc) cells?

A
  • they also need 3 signals
  • Th cells can provide signal 3 (cytokines)
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14
Q

what do Tc (CD8) cells do?

A
  • MHC I recognition pathway
  • release perforin and granzymes to lyse infected and cancer cells
  • production of antiviral and inflammatory cytokines
  • once activated, only need signal 1 (antigen recognition) to kill
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15
Q

how do B cells convert to Bm cells and plasma cells?

A
  • ‘class switching’ - stimulated by IL-4
  • IgM antibodies convert to other isotypes (irreversible)
  • joining of variable, diversity and joining (VDJ) segments in diff combinations
  • type of PAMP determines which isotype will be produced
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16
Q

distribution of antibody isotypes

A
  • IgG: blood, can cross placenta (second responder, high affinity)
  • IgA (dimer): mucosa + breast milk
  • IgD: signal B cells to be activated - BCR
  • IgM (pentamer): blood and lymph - first responder - BCR, low affinity
  • IgE: mast cells, connective tissue
  • type and function determined by heavy chain
17
Q

functions of antibodies (PIAANOS)

A
  • precipitation: makes pathogens insoluble, allowing them to precipitate out
  • immobilisation
  • agglutination
  • activation of complement proteins and NK cells
  • neutralisation: blocking of pathogen binding or neutralising toxins
  • opsonisation: enhances phagocytosis and triggers complement proteins
  • sensitisation of mast cells: IgE binds and creates cross links > degranulation
18
Q

2 characteristics of antigens

A
  • immunogenicity: ability to stimulate lymphocytes to divide
  • reactivity: react with antibodies and immune system to result in an immune response