linking adaptive and innate L6 Flashcards
MHCs
TWO TYPES MHC1 MHC2, these are important for activating T/B cells to let know that these are pathogens to respond to
naive cells - never seen Ag before
MHC1
present intracellular antigens like viral proteins
found on all nucleated cells as all cells can be infected, lets immune system know its infected
recognised by CTL CD8+ receptors
triggers killing of infected cells
MHC2
presents extracellular antigens like bacterial antigens
only found on APCs - macrophage, B and DC, as need phagocytosis for this
recognised by Treg/Th CD4+ receptors
coordinate immune responses, secretes IFN-Y etc.
MHC are diverse
need a wide range to present a wide range of antigens, the more diverse the better
MHC alleles are codominant so halo-type is set of MHC cells on each chromosome
MHC define accepting or rejection of grafts as foreign MHC molecules in graft may activate recipient T cells which kills graft, so need to match holotype
these are highly polymorphic
To fully activate T cells requires 2 signals
signal 1- MHC-Ag with TCR
signal 2 - co stimulation due to DAMPS causing upregulation of B7, which binds to CD28 on T cells to say this microbe is from a pathogen and need to activate to respond
without this, no activation and T cell dies or deactivates, this ensures that if presenting self-antigen, no response
macrophages APC
activates Th cells to then produce IFN-Y which increase macrophage activation
B cell as APC
need permission from previous activated Th, ones already activated by DC in order to activate
DC as APC
sample, traveller and presented
T-dependent Ab respond
B cells when acting as APC do so, so they can be activated, but can only do this with a previously activated Th cell.
This Th cell binds to the same antigen it did on the DC/MACRO so knowns its a pathogen
this allows full effector functions of B cell, switching isotopes and affinity maturation and long lasting respond
t-indepdent Ab response
B cell can activate without this but limited effector functions, no isotope switching so remains IgM, normally stimulated by PAMPs
activation of immune memory cells
much easier to activate and can be activated by more APC types, not just DC
resolving immune response
As infection clears, less DAMPS/PAMPS, less antigens, less presentation and less activating, less B7 signals
Treg cells develop and IL-10 cytokines for inhibitory effects to control and stop response