Lecture 32 - NK Cells II Flashcards

1
Q

Outcome of alloreactive donor-derived NK cells (bone marrow transplant)
1)
2)
3)

A

1) Better engraftment
2) Better leukaemia control
3) No graft versus host disease

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

CD158 receptors that inhibit NK cell killing

A

Only CD158 with long (L) tails have ITIMs, which are what inhibit NK cell killing

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

What controls NK cell activity?

A

A combination of stimulatory and inhibitory signals

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

NK cell activating receptors
1)
2)
3)

A

1) CD158(s)
2) CD16
3) NKG2D

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

NK cell inhibitory receptors
1)
2)
3)

A

1) CD158(l)
2) Ly49
3) MHCI

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

Why do patients receiving a bone-marrow transplant with alloreactive NK cells have no graft-versus-host disease?
1)
2)

A

1) NK cell mismatch leads to killing of DCs in periphery

2) Non-donor bone marrow-derived DCs can no longer activate T cells against self MHCII

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q
Cause of graft-versus-host disease
1)
2)
3)
4)
5)
A

1) Dendritic cells are bone-marrow derived, therefore are derived from donor bone marrow
2) DCs are responsible for negative selection of T cells
3) Cortical epithelial cells aren’t bone-marrow derived
4) There will be no negative selection of T cells that react to MHCII from host
5) DCs from periphery (that display host MHCII) activate T cells, which then go and kill self cells inperiphery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q
NK cell receptors that activate NK cells
1)
2)
3)
4)
A

1) Adhesion molecules CD2, 2B4
2) Natural cytotoxicity receptors NKp30, NKp44, NKp46
3) Activating forms of CD158, Ly49
4) NKG2D

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

CD2 and 2B4 ligands

A

On haematopoietic cells.

This might be why NK mismatch is so effective against leukaemias

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

Activating forms of Ly49, CD158 ligands

A

Unknown.

Might be MHCI

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

which cells express NKG2D?

A

All NK cells, some T cells

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

NKG2D effects
1)
2)
3)

A

1) Potent activator of NK cells
2) T cell costimulation (gamma/delta and CD8+)
3) Enhanced TNFa and NO activity in macrophages

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

Human NKG2D ligands
1)
2)

A

1) MIC A/B

2) ULBP

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

Murine NKG2D ligands
1)
2)

A

1) Retinoid acid early inducible transcripts (RAE-1)

2) H60

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

Common features of NKG2D ligands
1)
2)
3)

A

1) All MHCI-like (two alpha helices over a beta sheet)
2) Don’t bind peptides
3) Don’t bind beta2-microglobulin

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

Why can’t NKG2D ligands bind peptide?

A

The binding groove is too narrow

17
Q

NKG2D ligand expression
1)
2)
3)

A

1) Inducible (not constitutive)
2) Low or absent expression in most adult tissues
3) Induced by cellular stress

18
Q
What can induce NKG2D expression?
1)
2)
3)
4)
5)
6)
A

1) Cellular stress, in response to metabolic perturbations
2) Heat shock
3) Viral infection (EG: CMV)
4) Mycobacterial infection
5) Pathogenic E coli
6) Tumour cells

19
Q

Which intracellular factors initiate NKG2D-ligand expression?

A

Protein kinases ATM and ATR

20
Q

What causes protein kinases ATM and ATR to induce NKG2D-ligand expression?
1)
2)
3)

A

1) DNA damage
2) dsDNA breaks
3) Stalled replication forks

21
Q

What can override NK cell inhibitory signals?

A

NKG2D signals

Allows NK cells to kill target cell, even if target cell expresses MHCI

22
Q

CMV infection natural history
1)
2)

A

1) Replicates in the liver and spleen between days 1 and 8-10
2) Establishes a chronic infection in the salivary glands

23
Q

Host genes that can regulate CMV infection
1)
2)

A

1) Ly49H in mice

2) CD94- NKG2C+ in humans (maybe)

24
Q

Mouse strain that has high CMV titres in spleen and liver, but ultimately clears virus

25
Mouse strain that has low CMV titres in spleen and liver, but has a chronic
C57B6
26
Ly49H ligand
Recognises m157, and MHCI-like molecule expressed by murine CMV
27
What does Ly49H signal through?
DAP12, a CD3-like receptor adaptor molecule that contains ITAMs
28
Mice that Ly49H is present in
C57B6
29
Evidence for NK cell oligoclonal expansion
In mice with mCMV, Ly49H+ NK cells are preferentially expanded
30
Evidence for NK cell memory 1) 2)
1) After an infection with mCMV, C57B6 mice have greater levels of Ly49H+ NK cells than before infection 2) Greater proportion of 'memory' NK cells secrete IFNg than non-memory
31
Do NK cells undergo contraction after expansion?
Yes. | Similar to a CD8+ response
32
Why does CMV express m157 if it is recognised by NK cells?
Allows virus to establish a chronic infection in salivary glands
33
``` Effects of mCMV in mice without Ly49H 1) 2) 3) 4) ```
1) Elevated viral load 2) More antigen 3) Robust T cell response 4) More effective viral clearance
34
``` Effects of mCMV in mice with Ly49H 1) 2) 3) 4) 5) ```
1) Better acute control of virus 2) Less pathology 3) Increased killing of infected DCs 4) Impaired T cell responses (from killed DCs) 5) Viral persistence
35
Interleukin that allows NK cell expansion
IL-12
36
``` Ways to activate NK cells 1) 2) 3) 4) ```
1) Missing self 2) Induced self 3) Direct recognition of viral glycoproteins 4) Cytokine-dependent activation
37
``` Cytokines that activate NK cells 1) 2) 3) 4) ```
1) IFNa 2) IL-12 3) IL-15 4) IL-18