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Immunomodulation to treat
atherosclerotic disease
G. Pasterkamp, UMCU, Utrecht,
the Netherlands
Atherosclerosis and inflammation
Hansson GK
N Engl J Med
2005;352:1685-95
Immunomodulation and
atherosclerosis
• Immunosuppression
– Cyclosporin (Emeson et al. Am J path 1993)
– Transfer of CD4+ cells in Apo E mice
Zhou X et al.
Circulation 2000
Immunomodulation and
atherosclerosis
• Immunosuppression
– Cyclosporin (Emeson et al. Am J path 1993)
– Transfer of CD4+ cells in Apo E mice
– Transfer of B2GP-I lymphocytes in LDL-R
mice (George J et al. Circulation 2000)
– Antibodies against CD40 and CD40 L
Anti CD40L in LDL-R
mouse.
Mach F et al,
Nature 1998
CD154 -/-/ ApoE -/-
Lutgens et al
Nature Med 1999
Immunomodulation and
atherosclerosis
• Active immunization
– LDL modified epitopes
Palinski et al. PNAS 1995, LDL-R rabbit
MDA =malondialdehyde-LDL
Hypercholesterolemic
rabbit,
Ameli S et al.
ATVB 1996
Immunomodulation and
atherosclerosis
• Active immunization
– LDL modified epitopes
• Passive immunisation
– IgG
– Antibodies Against Aldehyde-Modified
Apolipoprotein B-100 Peptide Sequences
ivIg reduces fatty streak formation in apo E KO mice
Nicoletti A et al
J Clin Invest 1998
Antibodies Against Aldehyde-Modified Apolipoprotein B-100
Schiopu et al.
Circulation 2004
Mice were treated with different doses of IEI-E3 (red) or FITC-8 (blue)
antibodies. Values on y axis represent oil red O–stained areas as percentage
of total descending aorta area..
Immunomodulation and
atherosclerosis
• Active immunization
– LDL modified epitopes
• Passive immunisation
– IgG
– Antibodies Against Aldehyde-Modified Apolipoprotein B-100
Peptide Sequences
• Interleukin-12 (IL-12) has been identified as a key
inducer of a type 1 T-helper cell cytokine pattern.
Blockade of interleukin-12 function by protein vaccination
attenuates atherosclerosis. (Hauer et al. Circulation 2005)
• Cytokine network manipulation
Immunomodulation and
atherosclerosis
• Induction of tolerance
– Influencing Toll Like Receptor Responsiveness.
Toll-like receptors
• Innate immune system
• First line of defense
• Receptors for pathogen-associated
patterns
• Family of 10 receptors in human
• Toll-like receptor 2 and 4 most attention in
the cardiovascular field
Toll-like receptor pathway
NODs: intracellular proteins involved in inflammation
Inflammatory cytokines
TLR2
TLR1
or
TLR6
MyD88
TIRAP/Mal
IRAK
TRAF6
NEMO/IKKκ
IKKα
IKKβ
NF- κB
NF- κB
Immunomodulation and
atherosclerosis
• Induction of tolerance
– Influencing Toll Like Receptor Responsiveness.
• Cross-tolerance TLR2 and TLR4
• Surgery influences endotoxin responsiveness (Lemaire et al J Clin
Imunology 1998)
Pretreatment with LPS results in impaired infarct
size in animal experimental model
Eising et al
Cardiovasc Res 1996
cTnT release in a model of myocardial ischemia of the LAD
in the anesthetized rat
Zacharowski et al
ATVB 1999
1a- patients with a history of UA and persisting complaints
1b- patients with a history of UA who were free of symptoms
2- patients with chronic angina
3- healthy volunteers
Liuzzo et al
Circulation 2001
Methods
• Patients scheduled for percutaneous coronary
intervention (PCI) in the morning included after
informed consent was signed
• Bloodsamples drawn immediately after sheath
insertion and 2 hours after procedure
• Clinical questionnaires, data from patient file and
angiographic data
Results
• 100 patients included
• 20 patients excluded:
– 5 patients without 2nd bloodsample
– 2 patients with intravenous corticosteroids excluded
– In 13 patients no balloon dilatation was performed
due to negative FFR, unpassable lesion or
impossibility to visualize coronary lesion
• Flowcytometry of TLR2 and TLR4
TLR2 response after 5000 ng/ml Pam3Cys
0
200
400
600
TNF-αconcentration(pg/ml)
p < 0.01
before
PTCA
2h after
PTCA
TLR4 response after 100 ng/ml LPS
0
1000
2000
3000
4000
5000
TNF-αconcentration(pg/ml)
p < 0.01
before
n=80
after
n=80
TLR2 response (Pam3Cys)
mean TNF-α (±SEM)
n=80
stimulatory
ligand before after p
Pam3Cys
5000 ng/ml
159
(±20)
68
(±10)
<0,01
Pam3Cys
500 ng/ml
68
(±9)
32
(±5)
<0,01
Pam3Cys
50 ng/ml
41
(±5)
20
(±4)
<0,01
TLR4 response (LPS)
mean TNF-α (±SEM)
n=80
stimulatory
ligand before after p
LPS 1000
ng/ml
2338
(±161)
1957
(±147)
<0,01
LPS 100
ng/ml
1723
(±128)
1271
(±112)
<0,01
LPS 10
ng/ml
893
(±83)
519
(±51)
<0,01
TLR2 expression
before after p
TLR2 on
granulocytes
0,73
(±0,02)
0,70
(±0,02)
0,01
TLR2 on
monocytes
3,30
(±0,19)
2,90
(±0,12)
<0,01
TLR4 expression
before after p
TLR4 on
granulocytes
0,61
(±0,02)
0,59
(±0,01)
0,65
TLR4 on
monocytes
3,31
(±0,19)
2,87
(±0,19)
0,05
TLR4 response without dilatation
0
1000
2000
3000
4000
5000
TNF-αconcentration(pg/ml)
before,
n=13
after,
n=13
TLR2 response without dilatation
0
200
400
600
TNF-αconcentration(pg/ml)
*
before,
n=13
after,
n=13
TLR2 response without dilatation
before after p
TLR2 on
granulocytes
0,82
(±0,08)
0,79
(±0,08)
0,26
TLR2 on
monocytes
4,16
(±0,57)
3,82
(±0,52)
0,08
Summary
• Coronary balloon dilatation decreases
responsiveness of TLR2 and 4
• Coronary balloon dilatation decreases
expression of TLR2 and TLR4 on individual
granulocytes and monocytes
• These effects were also evident but less
pronounced in patients with less traumatic
intervention
TNF-αconcentrationafter10ng/mlLPS
percentage diameter stenosis
percentage diameter stenosis in relation to TLR4 response
51-70% 71-90% 91-99% 100%
0
1000
2000
3000
4000
5000
6000





Inhibition of TLR receptor and cytokine signaling-
A unifying theme in ischemic tolerance
(Kariko et al J Cerebral Blood flow &Metabolism, 2004)
• Protection against effects (inflammatory responses) of
acute ischemia by TLR tolerance induction.
Conclusion
Baseline responsiveness or tolerance of the
innate immune system upon ligand
stimulation differs among patients.
Understanding the mechanisms of tolerance
development of the innate immune system
may provide new targets for intervention
Tracey KJ, Nature. 2002 Dec 19-26;420(6917):853-9
The Immune reflex
Cholinergic
anti-inflammatory pathway
• ACh prevents release of pro-inflammatory
cytokines like TNF in macrophages
• Direct electrical vagal stimulations inhibits
TNF synthesis in RES
• Vagotomy exacerbates TNF response to
inflammatoy stimuli

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Immunomodulation to Treat Atherosclerotic Disease by Inducing Tolerance in Toll-Like Receptors

  • 1. Immunomodulation to treat atherosclerotic disease G. Pasterkamp, UMCU, Utrecht, the Netherlands
  • 2. Atherosclerosis and inflammation Hansson GK N Engl J Med 2005;352:1685-95
  • 3. Immunomodulation and atherosclerosis • Immunosuppression – Cyclosporin (Emeson et al. Am J path 1993) – Transfer of CD4+ cells in Apo E mice
  • 4. Zhou X et al. Circulation 2000
  • 5. Immunomodulation and atherosclerosis • Immunosuppression – Cyclosporin (Emeson et al. Am J path 1993) – Transfer of CD4+ cells in Apo E mice – Transfer of B2GP-I lymphocytes in LDL-R mice (George J et al. Circulation 2000) – Antibodies against CD40 and CD40 L
  • 6. Anti CD40L in LDL-R mouse. Mach F et al, Nature 1998 CD154 -/-/ ApoE -/- Lutgens et al Nature Med 1999
  • 7. Immunomodulation and atherosclerosis • Active immunization – LDL modified epitopes
  • 8. Palinski et al. PNAS 1995, LDL-R rabbit MDA =malondialdehyde-LDL
  • 10. Immunomodulation and atherosclerosis • Active immunization – LDL modified epitopes • Passive immunisation – IgG – Antibodies Against Aldehyde-Modified Apolipoprotein B-100 Peptide Sequences
  • 11. ivIg reduces fatty streak formation in apo E KO mice Nicoletti A et al J Clin Invest 1998
  • 12. Antibodies Against Aldehyde-Modified Apolipoprotein B-100 Schiopu et al. Circulation 2004 Mice were treated with different doses of IEI-E3 (red) or FITC-8 (blue) antibodies. Values on y axis represent oil red O–stained areas as percentage of total descending aorta area..
  • 13. Immunomodulation and atherosclerosis • Active immunization – LDL modified epitopes • Passive immunisation – IgG – Antibodies Against Aldehyde-Modified Apolipoprotein B-100 Peptide Sequences • Interleukin-12 (IL-12) has been identified as a key inducer of a type 1 T-helper cell cytokine pattern. Blockade of interleukin-12 function by protein vaccination attenuates atherosclerosis. (Hauer et al. Circulation 2005) • Cytokine network manipulation
  • 14. Immunomodulation and atherosclerosis • Induction of tolerance – Influencing Toll Like Receptor Responsiveness.
  • 15. Toll-like receptors • Innate immune system • First line of defense • Receptors for pathogen-associated patterns • Family of 10 receptors in human • Toll-like receptor 2 and 4 most attention in the cardiovascular field
  • 16. Toll-like receptor pathway NODs: intracellular proteins involved in inflammation Inflammatory cytokines TLR2 TLR1 or TLR6 MyD88 TIRAP/Mal IRAK TRAF6 NEMO/IKKκ IKKα IKKβ NF- κB NF- κB
  • 17. Immunomodulation and atherosclerosis • Induction of tolerance – Influencing Toll Like Receptor Responsiveness. • Cross-tolerance TLR2 and TLR4 • Surgery influences endotoxin responsiveness (Lemaire et al J Clin Imunology 1998)
  • 18. Pretreatment with LPS results in impaired infarct size in animal experimental model Eising et al Cardiovasc Res 1996
  • 19. cTnT release in a model of myocardial ischemia of the LAD in the anesthetized rat Zacharowski et al ATVB 1999
  • 20. 1a- patients with a history of UA and persisting complaints 1b- patients with a history of UA who were free of symptoms 2- patients with chronic angina 3- healthy volunteers Liuzzo et al Circulation 2001
  • 21. Methods • Patients scheduled for percutaneous coronary intervention (PCI) in the morning included after informed consent was signed • Bloodsamples drawn immediately after sheath insertion and 2 hours after procedure • Clinical questionnaires, data from patient file and angiographic data
  • 22. Results • 100 patients included • 20 patients excluded: – 5 patients without 2nd bloodsample – 2 patients with intravenous corticosteroids excluded – In 13 patients no balloon dilatation was performed due to negative FFR, unpassable lesion or impossibility to visualize coronary lesion • Flowcytometry of TLR2 and TLR4
  • 23. TLR2 response after 5000 ng/ml Pam3Cys 0 200 400 600 TNF-αconcentration(pg/ml) p < 0.01 before PTCA 2h after PTCA
  • 24. TLR4 response after 100 ng/ml LPS 0 1000 2000 3000 4000 5000 TNF-αconcentration(pg/ml) p < 0.01 before n=80 after n=80
  • 25. TLR2 response (Pam3Cys) mean TNF-α (±SEM) n=80 stimulatory ligand before after p Pam3Cys 5000 ng/ml 159 (±20) 68 (±10) <0,01 Pam3Cys 500 ng/ml 68 (±9) 32 (±5) <0,01 Pam3Cys 50 ng/ml 41 (±5) 20 (±4) <0,01
  • 26. TLR4 response (LPS) mean TNF-α (±SEM) n=80 stimulatory ligand before after p LPS 1000 ng/ml 2338 (±161) 1957 (±147) <0,01 LPS 100 ng/ml 1723 (±128) 1271 (±112) <0,01 LPS 10 ng/ml 893 (±83) 519 (±51) <0,01
  • 27. TLR2 expression before after p TLR2 on granulocytes 0,73 (±0,02) 0,70 (±0,02) 0,01 TLR2 on monocytes 3,30 (±0,19) 2,90 (±0,12) <0,01
  • 28. TLR4 expression before after p TLR4 on granulocytes 0,61 (±0,02) 0,59 (±0,01) 0,65 TLR4 on monocytes 3,31 (±0,19) 2,87 (±0,19) 0,05
  • 29. TLR4 response without dilatation 0 1000 2000 3000 4000 5000 TNF-αconcentration(pg/ml) before, n=13 after, n=13
  • 30. TLR2 response without dilatation 0 200 400 600 TNF-αconcentration(pg/ml) * before, n=13 after, n=13
  • 31. TLR2 response without dilatation before after p TLR2 on granulocytes 0,82 (±0,08) 0,79 (±0,08) 0,26 TLR2 on monocytes 4,16 (±0,57) 3,82 (±0,52) 0,08
  • 32. Summary • Coronary balloon dilatation decreases responsiveness of TLR2 and 4 • Coronary balloon dilatation decreases expression of TLR2 and TLR4 on individual granulocytes and monocytes • These effects were also evident but less pronounced in patients with less traumatic intervention
  • 33. TNF-αconcentrationafter10ng/mlLPS percentage diameter stenosis percentage diameter stenosis in relation to TLR4 response 51-70% 71-90% 91-99% 100% 0 1000 2000 3000 4000 5000 6000     
  • 34. Inhibition of TLR receptor and cytokine signaling- A unifying theme in ischemic tolerance (Kariko et al J Cerebral Blood flow &Metabolism, 2004) • Protection against effects (inflammatory responses) of acute ischemia by TLR tolerance induction.
  • 35. Conclusion Baseline responsiveness or tolerance of the innate immune system upon ligand stimulation differs among patients. Understanding the mechanisms of tolerance development of the innate immune system may provide new targets for intervention
  • 36. Tracey KJ, Nature. 2002 Dec 19-26;420(6917):853-9 The Immune reflex
  • 37. Cholinergic anti-inflammatory pathway • ACh prevents release of pro-inflammatory cytokines like TNF in macrophages • Direct electrical vagal stimulations inhibits TNF synthesis in RES • Vagotomy exacerbates TNF response to inflammatoy stimuli