IMMUN: Adaptive Immunity Flashcards
1
Q
epitope
A
- part of the antigen that binds to the antibody
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)
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
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
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
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
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
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
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
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
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)
12
Q
lineage of T cells
A
13
Q
how do CD4 (Th) cells activate CD8 (Tc) cells?
A
- they also need 3 signals
- Th cells can provide signal 3 (cytokines)
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
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
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