Brainscape's Knowledge GenomeTM

Browse over 1 million classes created by top students, professors, publishers, and experts.


See full index

HH M2 CA1 Immunology > Immunology 07. Immune Tolerance > Flashcards

Immunology 07. Immune Tolerance Flashcards

1
Q
A
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q
A

C is wrong. Should be binding to self-peptide and self-antigen.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Autoimmune diseases are associated with what mutation?

A

Autoimmune diseases are associated with what mutation?

Mutations in AIRE/FOXp3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Best examples of Tregs? And what is their transcription factor?

A

Best examples of Tregs? And what is their transcription factor?

CD4+ CD25+ T cells. Transcription factor: Foxp3

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Costimulation signal comes from?

A

Costimulation signal comes from?

1) CD28 on T cells
2) B7 on APC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Define Immune tolerance?

A

Define Immune tolerance?

Mechanisms that prevent adaptive immune responses to self antigens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Effects of Costimulation? (IMPT!!!)

A

Effects of Costimulation? (IMPT!!!)

Proliferation and differentiation signal

Upregulation of IL-2 production by T Cells -> T cells proliferation, differentiation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Essentially linking Immune checkpoint and MMR

A

Essentially linking Immune checkpoint and MMR
Immune checkpoint-> natural process that prevents damage from chronic infection

We propose that we could block the effects of the checkpoint -> so that we can kill of cancer

But immune blockades have its side effects –> reverse peripheral tolerance –> autoimmunity

Notably useful in patients with MMR defects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How can we enhance T cell function with respect to CTLA4?

A

How can we enhance T cell function with respect to CTLA4?

We can have Anti-CTLA4 antibody

Depletes Tregs and block inhibitory effect of CTLA4 on effector t cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How do we enhance anti-tumour t cell responses with respect to ctla-4 and pd1?

A

How do we enhance anti-tumour t cell responses with respect to ctla-4 and pd1?

Antibodies that block these molecules!!

Diminish inhibitory signals for T cells-> Boost anti-tumour T cells responses-> tumour regression

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How does Autoimmune regulator (AIRE) work?

A

How does Autoimmune regulator (AIRE) work?

Allows us to transiently express extra-thymic tissue-specific antigens in the thymus.

Allows for negative selection of TCRs specific for self antigens that are normally not expressed in the thymus

Think about it. How does the thymus select for T cells which wont bind to and recognise self antigens outside of the thymus??? Thymus got the whole body’s repetoire of self antigens meh??? Have. AIRE :)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How does Central Tolerance of T cells work?

A

How does Central Tolerance of T cells work?

Essentially, after somatic recombination which results in a plethora of different antigen receptors, the body selects for useful receptors and discards useless and dangerous receptors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How does defective Mismatch Repair (MMR) cause high tumour mutational burden? What is it even

A

How does defective Mismatch Repair (MMR) cause high tumour mutational burden? What is it even

TLDR; DEFECTIVE -> NEOPLASTIC TRANSFORMATION

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

How does Regulation happen?

A

How does Regulation happen?

Via Regulatory T cells inhibiting immune response

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How does Treg act out its function?

A

How does Treg act out its function?

Possess **strong TCRs **that recognises SP-SMHC strongly, and act on self-reactive immune cells to suppress their activity

This is the balance that the immune system needs to control the other T cells after danger is gone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

In what type of cells do we see Programmed Death-1 (PD-1). What are the effects?

A

In what type of cells do we see Programmed Death-1 (PD-1). What are the effects?

In chronically activated T cells.

Inhibits activation signalling from TCR complex and CD28

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Mutation in foxp3 is associated with?

A

Mutation in foxp3 is associated with?

Multi-organ autoimmune disease

18
Q

positive and negative selection follows the principle of which childhood story?

A

positive and negative selection follows the principle of which childhood story?

Goldilock’s porridge.

Too cold not nice
Too hot will hurt you :)

19
Q

Revision: 3 signals needed for NAIVE t cell activation?

A

Revision: 3 signals needed for NAIVE t cell activation?

1) Specific antigen signal (TCR:antigen-MHC complex)
2) Co-stimulation signal (B7:CD28)
3) Cytokines signal (IL2, etc)

20
Q

Role of PD-1?

A

Role of PD-1?

1) Limits T cell mediated tissue damage during chronic/persistent infections
2) Inhibits autoreactive T cells

Blocks TCR & CD28 signalling

21
Q

Similarities and differences between CTLA-4 and CD28? (IMPT)

A

Similarities and differences between CTLA-4 and CD28? (IMPT)

Similarities:
- Both expressed on T cells
- Both binds to B7

Differences:
- CTLA4 not constitutive, comes up a few days after T cell activation
- CTLA4 binds more strongly to B7 than CD28
- Interaction between CTLA4:B7 delivers negative signal while that between CD28:B7 delivers positive signal

22
Q

Treg constitutively express which molecule?

A

Treg constitutively express which molecule?

CTLA-4.

Sequestration of B7 + Downreg B7 expression on APCs

23
Q

What are some other possible mechanisms of Treg carrying out its function other than via TCR?

A

What are some other possible mechanisms of Treg carrying out its function other than via TCR?
Cell-cell contact: Constitutive expression of CTLA4 on Tregs blocks and removes B7 from APCs

Soluble factors: Secrete inhibitory cytokines: TGF-B

These are the things that tumour cells try to mimic!!

24
Q

What are some PRR (pattern recognition receptors) that innate immune system has?

A

What are some PRR (pattern recognition receptors) that innate immune system has?

1) TLR
2) Lectin
3) NOD-like receptor
4) RIG-like receptor

PRR = Pattern Recognition Receptors

25
Q

What are the 3 mechanisms of peripheral tolerance? (IMPT!!!)

A

What are the 3 mechanisms of peripheral tolerance? (IMPT!!!)

1) Ignorance: no signal 1
2) Anergy: signal 1 delivered, but no signal 2 (yes TCR signal but no Costimulatory signal)
3) Regulation: Treg

26
Q

What are the adverse effects of immune checkpoint blockade?

A

What are the adverse effects of immune checkpoint blockade?

1) Not antigen specific
2) Leads to reversal of peripheral tolerance of t cells to self antigens-> increased autoimmune damage to organs

Essentially, Immune checkpoint blockade is a proposed therapy for some patients with immunological disease/cancers

Patients with MMR deficiency seems to respond well to immune checkpoint blockade

27
Q

What are the detriments and benefits of defective MMR?

A

What are the detriments and benefits of defective MMR?

Detriment: Enhances mutagenesis

Benefit: Enhanced mutagenesis could generate specific tumour neoantigens that can be recognised by adaptive immune system as foreign antigens

28
Q

What are the two different subsets of immune tolerance?

A

What are the two different subsets of immune tolerance?

1) Central tolerance: when immature lymphocytes undergo selection process in primary lymphoid organ

2) Peripheral tolerance: mechanisms operating on mature lymphocytes in the periphery

29
Q

What does negative selection select for?

A

What does negative selection select for?

Basically selects for T cells with receptors that bind to self-peptide-self MHC complexes with high affinity to DIE by apoptosis

30
Q

What does positive selection in T cells select against?

A

What does positive selection in T cells select against?

T cells that do not have any form of binding to any self peptide-self MHC complexes in the thymus

31
Q

What does Positive selection select for?

A

What does Positive selection select for?

Lymphocytes which that express TCRs with SOME reactivity for Self-MHC, and thus exhibit MHC restriction

32
Q

What happens in Ignorance (PT)

A

What happens in Ignorance (PT)

Interaction between TCR and peptide-self MHC too weak to cause activation of mature T cells in periphery

33
Q

What happens to T cells when TCR binds to MHC-peptide complex?

A

What happens to T cells when TCR binds to MHC-peptide complex?

Survival signal

34
Q

What is anergy (PT)

A

What is anergy (PT)
Presence of specific antigen signal but not enough co-stimulatory signal.

Anergised cells remain unresponsive even if it subsequently receives signal 2 and signal 3. Makes sense if u look at the examples. if these types of T cells can be activated, means they are auto-reactive!!! Peripheral tolerance’s job is to weed out these type of self-reactive T cells!!!

Examples:
- T cells that binds to immature DCs
- T cells that binds to non-APC normal cells

35
Q

What is MHC restriction?

A

What is MHC restriction?

It means that TCRs without some ability to bind to self MHC would not be useful

36
Q

What is Pathogen associated molecular patterns?

A

What is Pathogen associated molecular patterns?

Essentially conserved molecular patterns shared by broad classes of pathogens

usually absent in sterile environment

37
Q

What kind of patients appear to respond well to immune checkpoint blockade?

A

What kind of patients appear to respond well to immune checkpoint blockade?

MMR deficiency

38
Q

What triggers DC maturation?

A

What triggers DC maturation?

Recognition of PAMPs (pathogen-associated molecular patterns)

39
Q

Which 2 types of contacts do we need to stabilise specific antigen interaction between t cell and APC?

A

Which 2 types of contacts do we need to stabilise specific antigen interaction between t cell and APC?

TCR-peptide
TCR-MHC

40
Q

With respect to CTLA4 and PD1, how can cancer evade immunity?

A

With respect to CTLA4 and PD1, how can cancer evade immunity?

Upreg CTLA4 or PD1 on tumour specific T cells
Expression of PDL1 on tumour cells
Inhibitory effect of Tregs

HH M2 CA1 Immunology (14 decks)

Brainscape helps you reach your goals faster, through stronger study habits.
© 2024 Bold Learning Solutions. Terms and Conditions