MHC Flashcards

1
Q

what do extracellular PAMPs trigger?

A

PRR to (capture, process & present - APC) to MHC II cells

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2
Q

what does MHC II lead to?

A

humoral immunity (antibodies - circulating, compliment)

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3
Q

what are examples of extracellular PAMPs?

A

parasite, worms, fungi, bacteria

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4
Q

what are examples of intracellular PAMPs?

A

virus, protozoa, bacteria

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5
Q

what does intracellular PAMPs trigger?

A

MHC I, CD4+ T cells

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6
Q

what does MHC II, CD4+ T cells lead to?

A

cell-dependent immunity (antibodies, complement, macrophage)

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7
Q

what is the difference between cell-dependent immunity (MHC II) and humoral immunity (CD8+)?

A

cell-dependent has macrophage involvement

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8
Q

where are MHC I found?

A

all nucleated cells

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9
Q

where is MHC II found?

A

dendritic cells (blood, mucous membranes, lymph nodes), macrophage, B cells

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10
Q

how do the antigen proteins enter the cell in MHC I (intracellular)?

A

pathogen makes own proteins in cells (endogenous proteins)
bacterial endogenous protein enters host cell and goes to proteosome (degrades bacterial protein into fragments) - 10-15AA

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11
Q

what happens to the small bacterial proteins in MHC I (after interaction with proteosome)?

A

enter the RER (via TAP transporters), where the bacterial protein is broken down even more (8-10AA)

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12
Q

where are MHC1 proteins made within the cell?

A

by ribosomes in RER

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13
Q

how does MHC 1 interact with small bacterial proteins?

A

MHC1 has peptide binding cleft (variable region) - temp covered
MHC1 chaperoned to TAP transporter (where bacterial protein broken down further)
MHC1 interacts with small bacterial peptide fragment (via peptide binding cleft) - unique, specific

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14
Q

what happens after MHC1 and small bacterial protein interaction if they are complimentary?

A

complex leaves RER via endosome –> golgi apparatus –> exocytosis, to be presented on cell surface (APC)

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15
Q

what happens after the complex is presented on cell surface (APC)?

A

wait for interaction with CD8+ T cell - specific interaction

if complimentary, then can trigger cell-dependent immunity (macrophage, antibodies, complement

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16
Q

what can intracellular PAMPs trigger?

A

MHC I via CD8+ T cells, but also MHC II –> cytotoxic T cells, release cytokines to kill infected cells

17
Q

what is special about an (MHC) APC cell?

A

can present lots of antigen peptide son 1 APC to interact with many MHC (specific)

18
Q

how does an extracellular PAMP enter the cell?

A

MHC II, CD4+ T cells (bacteria, fungi, parasites, worms)
pathogen in ECF circulating, recognised by macrophage
macrophage engulf via phagocytosis

19
Q

what happens after the macrophage has engulfed an extracellular PAMP?

A

lysosomes inside the cell (acidic environment) fuse with phagosome (bacterial engulfed)
form phagolysosome
acidic environment breaks down bacterial peptide (antigens)

20
Q

how is MHC II produced? where?

A

within the RER, ribosomes synthesising MHC II, chaperoned out of RER (by li), through golgi, form new endosome (slightly acidic)
(CLIP prevents antigens binding to peptide binding cleft - variable region)

21
Q

what happens after the lysosome has broken down the phagolysosome via acidic environment?

A

phagolysosome containing bacterial antigen fuse with MHC II - bind to peptide binding cleft (specific)

22
Q

what happens if the MHC II binds to phagolysosome?

A

the macrophage (APC) now presents the MHC II + antigen (complex) on it’s cell surface, awaiting interaction with CD4+ T cells (APC to be activated)

23
Q

what happens when a complimentary CD4+ cell interacts with MHC II?

A

the CD4+ T cell becomes T helper cell

promotes immunity by activating B cells

24
Q

what do CD4+ T cells and CD8+ T cells go onto become?

A

CD4+: T helper (activate B cells - immunity) - MHC II (extracellular)
CD8+: T killer (release cytokines, kill infected cells) - MHC I (intracellular)