Lec 11: MHCII and DCs Flashcards

1
Q

Read page 261 for the quiz

A

do it

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2
Q

If there are 10^15 different possible T cell receptors, how can 6 invariant molecules (MHCI = HLA-A, HLA-B, HLA-C and MHCII= HLA-DR, HLA-DQ, HLA-DP) have the capacit to present 10^15 peptides

A

Due to the extreme polymorphism at the species and individual level

Thousands of alleles that are co-dominantly expressed

Each cell can express 10^5 different MHC molecules

MHC binds anchor domains whcih ancohor peptides wiht different comformations

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3
Q

What is teh MHC complex also known as

A

the HLA (human leukocyte antigen) complex

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4
Q

What are the three major classes of molecules found encoded within the MHC locus

A

Class 1/2/3 MHC genes

as well as complents and inflammation proteins (MHC 3??)

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5
Q

MHC II structure

A

member of the ig superfamily

MHC II recombinaiton leads to heterodimeric proteins, with both a and b chains passing though the plasma membrane

a peptide bindng cleft is formed by the pairing//bridging of the a1 and b1 domains

accommodates peptides of 13-18 aa in length (these ones stick out of the cleft)

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6
Q

MHCII molecules exhibit polymorphism in the poptide binding region

MOTIFS and ANCHOR residues

A

MOTIF : common sequence in a peptide antigen that binds an MHC molecule less evident in MHC II peptides

ANCHOR RESIDUES: some aa anchor the peptide into the groove - not just localized to N and C termini for MHC II binding peptides

Extends other aa residues from groove to interact with TcRs - can be trimmed

peptide groove on both ends allows for 13-18 aa peptides

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7
Q

Promiscuous

A

a given MHC moleucle can bind numerous different peptides, and some pepties can bind to several different MHC molecules as long as they have a similar motif

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8
Q

what are the predominant MHC II types

A

DRB1

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9
Q

MHC II allelic variation in humans

A

again, transmitted in a haplotype.
-> allelic forms of MHC are inherited in linked groups known as haplotypes

one haplotype from the mother, and one from the father, moreover, each individual igg domain can undergo reassortment which increases flexibility with diffrent pairings

codominant expression of alleles

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10
Q

purpose of MHC diversity

A

provides flexibility in responding to unexpected environmental changes, now and in the future

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11
Q

MHC polymorphisms

A

pg 258-263

co-dominant expressionof both haplotypes
-> express foth a and b chains

HAPLOTYPES NAD RECOMBINAITON

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12
Q

Why are MHC polymorphisms important

A

survival of th species (not the individual)

lack of diversity in alleles can lead to population collapse because they are unable to protect themselves agaisnt pathogens

-> if only few MHC alleles are present the pathogen could mutate to gain a fitness advantage and we would die

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13
Q

Pathogen reproductiona nd MHC allele polymorphism

A

pathogens reproduce faster than humans and their mutation rate is higher.

  • > pathogens will always outpace teh counter evasion measures that involve MHC mutations
  • > the ultimate number of MHC types are limited

To counteract teh superior adaptability of pathogens humans must possess variants of each type of MHC molecules,

  • > moreover, not all MHC moleucles may protect an individual from infection -> may require a specific compliments/ pair
  • > a large number of MHC variants ensures that as a whole the population is protected from extinction
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14
Q

HLA DRB1 alleles affect the clinical course of chronic lymphocyte leukemia

A

see slides

antigens associated with the cancer are better presented on DRB1+

-> survival is haplotype dependent

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15
Q

Contrast the diversity of TCR/ BCR and MHC polymorphisms

A

Tcr and Bcr change in the individuals of a population (they are in constant fluc)

whereas the type and varient of MHC molecules does not vary in the lifetime of an individual

diveristy of MHC variants is at the population lelve

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16
Q

MHC II antigen processing

figure 7-17 on exam

A

MHC II presents extracellular antigen peptides

MHC II is primarily restricted to APCs

present peptides to CD4+ T cells

Different capability to present antigens may dicate overall strength of response from individual to individual

17
Q

HLA-DM

A

regulates peptide loading og MHC II molecules

their enzymatic fcn is to catalyze peptide cleavage

18
Q

HLA-DO

A

acts as a substrate mimic to competitively inhibit HLA-DM-mediated catalysis of MHC II peptide exchange

blocks peptide grove

  • > removed leaving CLP after digestion
  • > conformational change induces CLP to leave
  • > prevents any ol’ peptide from binding
19
Q

What are the roles of HLA-DM and HLA-DO

A

???

20
Q

Which receptors discriminate self and non-self peptides

A

TCR

Remember, MHC moleucles do not discriminate self and non-self peptides, this discrimination is the function of TCR

Loads Loads what ever is their in there microenvirome.
They then determine what if self or non self peptides have been loaded

21
Q

Recall, just beacuse it is presented, does not mean that it wil be recognized

A

T cells only recognize their cognate receptor/ antigen pair

DC’s however will express all sorts on antigen

22
Q

Stages of DC maturation

A

differentiation

antigen uptake and innate immune sensing

antigen processing and presentation

phenotype maturation (Cell surface markers)

Functional maturation (Cytokines and co-stimulaiton)

23
Q

DC phenotype maturation

A

change in cellular morphology

up-regulation of co-stimulatory molecules

CD86 (constitutive expression)

increase of CD80, a co-stimulatory molecule)

increase of ICOSL, a co-stimulatory molecule

increase of CD83, a marker of a mature DC

24
Q

DC functional maturation

A

ability of DC to activate T cells

presence and type of antigen presented

presences and type of co-stimulatory molecules

secretion and type of cytokines

25
Q

Give an example of a DC-T cell stimulatory activating or inhibiting signal

A

???

26
Q

Why does the DC maturation state matter

A

immature DCs express low levels of CD80/86 and strong ICOSL signals
-> stabalizes IL-10R on the surface of Naive T cells

IL-10 secretionby immature DCs promotes differentiation of anergic T cells or T regs

Mature DCs provide strong CD28 stimulation and promote effector T cell differentiation

see slides, but it basically determines if a T cell will be directed towards immunity or tolerance

27
Q

Dc migration to lymph node

A

need to stop picking up antigen before migration => want to present a ‘snap-shot’ of the microenviroment they came from

many DC types reside at the barrier sites such as the skin and mucosa surfaces

DC maturation dramatically enchances theri migratory capacity

  • > upregualtion of CCR7
  • > Traffic to T cell areas of secondary lymphoid organs

activated DCs cease any further antigen uptake
-> reflect the current state

28
Q

Distinct DC subsets are found in the blood, secondary lymphoid tissues as periphery

A

conventrional DC: antigen processing and presentation

langerhans cells: resident DCs in the skin

Plasmacytoid Dc: Major IFN producers in viral infection

Monocyte-derived DC: drive inflammation-> late to the party

29
Q

conventional DC

A

antigen processing and presentation

30
Q

langerhans cells

A

a type of DC

resident DCs in the skin

31
Q

Plasmacytoid DC

A

Major IFN producers in viral infection

32
Q

Monocyte-derived DC

A

drive inflamation and late to the party