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Non-Invasive
Macrophage Imaging for
Detection of Vulnerable Plaque
Applications and Limitations
Amersham
Morteza Naghavi, MD
A
B
Which one is
vulnerable, A or B?
The one with
inflammation
(macrophage infiltration)
Morphology vs. Activity Imaging
Inactive and
non-inflamed
plaque
Active and
inflamed
plaque
Similar in
IVUS OCT MRI
w/o CM
Morphology
Different
Activity
Thermography, Spectroscopy,
immunoscintigraphy, MRI with
targeted contrast media…
Plaque Morphology
vs.
Plaque Activity
We Need Both
Imaging Inflammation
- by MRI
- by CT
Both are available today!
Imaging Inflammation
- by MRI
Pioneered in 1980s
Rummeny E, Weissleder R, Stark DD, Elizondo G, Ferrucci JT.
Radiologe. 1988 Aug;28(8):380-6.
SuperparamagneticSuperparamagnetic
andand
Ultra-superparamagneticUltra-superparamagnetic
Iron OxideIron Oxide
lBlood pool Magnetic resonance (MR)
imaging contrast media with a central
core of iron oxide generally coated by a
polysaccharide layer
Shortening MR relaxation time
Engulfed by and accumulated in cells
with phagocytic activity
Particle Core Size Particle Size Blood
(nm) (nm) Half-life
Combidex 5-6 20-30 8h
Feridex 4-6 35-50 2.4±0.2h
DDM 43/34/102 6.4 20-30 6h
Clariscan
MION 4-6 17 varies
Feruglose
--- --- --- ---
Examples of commercially available SPIOs
USPIOs Enter the AtheroscleroticUSPIOs Enter the Atherosclerotic
Plaque ThroughPlaque Through
lMacrophages that engulfed
them
lFissured or thin cap
l Extensive angiogenesis
l vasa vasorum leakage
l Intra plaque hemorrhage
In-vitro Study of Macrophage
SPIO Uptake
 In a series of in-vitro studies we have tested
the rate of SPIO uptake by human activated
monocytes in different conditions regarding
incubation time and concentration of SPIO.
All SPIO were labeled by a fluorescent dye
(DCFA).
FL-labeled SPIO Incubated Macrophages 24hr
Double DAPI Staining with Fluorescence-labeled SPIO Macrophages
after 24hr Incubation
Hypothesis
vasa vasorum
Over magnification is a major advantage of SPIO
Darkening property of SPIO in the white background of fat
and water of plaque is another advantage
SPIO and T2 Effect
In-vitro study to show the effect of
macrophage SPIO uptake on their
T2 relaxation time
0
10
20
30
40
50
60
70
80
90
50 250 control
20 min
60 min
6 hours
24 hours
Macrophage Uptake of Feridex with Time
and Concentration Shown by T2 Reduction
Concentration µmol/ml
Histopathologic Studies of ApoE KO Mice
Injected with SPIO (Abdominal Aorta)
H&E staining
Iron Staining CD 68 staining
Iron particles
Histopathologic Study of Wild Type Mice
Injected With SPIO (Thoracic Aorta)
H&E staining
CD68 stainingIron staining
Comparison of the Number of the Iron Particles (per
HPF) in ApoE KO Mice Plaque vs. Normal Wall
0
5
10
15
Atherosclerotic
Aorta
Average
number of iron
particles per
sample
P <0.001
MR Image of Abdominal Aorta After SPIO
Injection in ApoE and Control Mice
ApoE
deficien
t mouse
C57B1
(control)
mouse
Before Injection After Injection (5 Days )
Dark (negatively enhanced) aortic wall, full of iron particles
Bright aortic lumen and wall without negative
enhancement and no significant number of iron particles
Injection of Cytokine Increases SPIO-Loaded Macrophage
Density in Aortic Plaques (Apo E Deficient Mice)
Naghavi et al Circulation 2003
Naghavi et al Circulation 2003
Injection of Cytokine Increases SPIO-Loaded Macrophage
Density in a Coronary Plaque (Apo E Deficient Mice)
Histopathologic studies of Thoracic aorta in Watanabe
Hereditary Hypercholesterolemic rabbit after SPIO injection
H&E staining
Iron staining
Iron staining
Histopathologic studies of Thoracic aorta in Watanabe
Hereditary Hypercholesterolemic rabbit after SPIO injection
H&E staining
Iron staining Iron staining
Iron particles
Plaque Cell Density vs SPIO
0
10
20
30
40
50
60
0 10 20 30 40 50 60 70
Cell Denity in H&E staining
SPIOpositivecell-Iron
staining
Series1
R=0.956
Correlation between Iron positive cells in Iron
staining and cell density in H&E staining in rabbit
atherosclerotic aorta.
MR Angiography 3D with Gadolinium-DTPA in
Watanabe Rabbit
Before SPIO injection After SPIO injection
MRI Identifies Plaque Inflammation by SPIO Nanoparticles
Watanabe rabbit
Post-SPIO
Watanabe rabbit
control
NZW rabbit
control
NZW rabbit
Post-SPIO
Watanabe Rabbit
Post-SPIO
Watanabe Rabbit
Control
NZW Rabbit
Post-SPIO
NZW Rabbit
Control
Ex-vivo MR study of the thoracic aorta in Watanabe and
Wild type rabbit after SPIO injection compared to control.
(Gradient echo)
Watanabe rabbit
Post-SPIO
Watanabe rabbit
control
NZW rabbit
Post-SPIO
NZW rabbit
control
Schmitz et al
Schmitz et al
Schmitz et al
Ruhem et al
Ruhem et al
Ruhem et al
Ruhem et al
Ruhem et al
Kooi et al
Kooi et al
Kooi et al
Kooi et al
Ho et al
Ho et al
MR signal changes after CsA treatment. A group with allotransplants was treated with CsA for either 7 days
(n=5) or 4 days (n=5) after initial MRI experiments showed decrease of MR signal intensity according to degree
of graft rejection. On POD 14, transplanted rats were reinjected with USPIO particles, and then MRI
experiments were performed. Animals treated 7 days showed minimal changes in MR signal intensity 24 hours
after reinjection (A and B), and animals treated 4 days showed MR signal intensity that was significantly
decreased after USPIO injection (C and D). MR images of short-axis view of graft are shown. MR images before
USPIO infusion are at A and C, and images taken 24 hours after infusion are at B and D.
Ho et al
Ho et al
• Imaging Macrophage
Activity in the Brain Using
Ultrasmall Particles of Iron
Oxide
Jeff W.M. Bultea and Joseph A. Franka Laboratory of Diagnostic
Radiology Research National Institutes of Health Bethesda, MD
• SPIO MR imagine of macrophage is
feasible for clinical applications.
• It will be of great interest to
investigate the cost-effectiveness of
this technique in comparison with
alternative diagnostic approaches.
Conclusion
• Poor spatial and temporal
resolution for coronary
applications
• Cost
• Cumbersome (injection and
delayed imaging)
Limitations

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Spio mri studies by dr naghavi-presented to ge-amersham

  • 1. Non-Invasive Macrophage Imaging for Detection of Vulnerable Plaque Applications and Limitations Amersham Morteza Naghavi, MD
  • 2.
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  • 4. A B
  • 5. Which one is vulnerable, A or B? The one with inflammation (macrophage infiltration)
  • 6. Morphology vs. Activity Imaging Inactive and non-inflamed plaque Active and inflamed plaque Similar in IVUS OCT MRI w/o CM Morphology Different Activity Thermography, Spectroscopy, immunoscintigraphy, MRI with targeted contrast media…
  • 8. Imaging Inflammation - by MRI - by CT Both are available today!
  • 9. Imaging Inflammation - by MRI Pioneered in 1980s Rummeny E, Weissleder R, Stark DD, Elizondo G, Ferrucci JT. Radiologe. 1988 Aug;28(8):380-6.
  • 10. SuperparamagneticSuperparamagnetic andand Ultra-superparamagneticUltra-superparamagnetic Iron OxideIron Oxide lBlood pool Magnetic resonance (MR) imaging contrast media with a central core of iron oxide generally coated by a polysaccharide layer Shortening MR relaxation time Engulfed by and accumulated in cells with phagocytic activity
  • 11. Particle Core Size Particle Size Blood (nm) (nm) Half-life Combidex 5-6 20-30 8h Feridex 4-6 35-50 2.4±0.2h DDM 43/34/102 6.4 20-30 6h Clariscan MION 4-6 17 varies Feruglose --- --- --- --- Examples of commercially available SPIOs
  • 12. USPIOs Enter the AtheroscleroticUSPIOs Enter the Atherosclerotic Plaque ThroughPlaque Through lMacrophages that engulfed them lFissured or thin cap l Extensive angiogenesis l vasa vasorum leakage l Intra plaque hemorrhage
  • 13. In-vitro Study of Macrophage SPIO Uptake  In a series of in-vitro studies we have tested the rate of SPIO uptake by human activated monocytes in different conditions regarding incubation time and concentration of SPIO. All SPIO were labeled by a fluorescent dye (DCFA).
  • 14. FL-labeled SPIO Incubated Macrophages 24hr
  • 15. Double DAPI Staining with Fluorescence-labeled SPIO Macrophages after 24hr Incubation
  • 17. vasa vasorum Over magnification is a major advantage of SPIO Darkening property of SPIO in the white background of fat and water of plaque is another advantage
  • 18. SPIO and T2 Effect In-vitro study to show the effect of macrophage SPIO uptake on their T2 relaxation time
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  • 20. 0 10 20 30 40 50 60 70 80 90 50 250 control 20 min 60 min 6 hours 24 hours Macrophage Uptake of Feridex with Time and Concentration Shown by T2 Reduction Concentration µmol/ml
  • 21. Histopathologic Studies of ApoE KO Mice Injected with SPIO (Abdominal Aorta) H&E staining Iron Staining CD 68 staining Iron particles
  • 22. Histopathologic Study of Wild Type Mice Injected With SPIO (Thoracic Aorta) H&E staining CD68 stainingIron staining
  • 23. Comparison of the Number of the Iron Particles (per HPF) in ApoE KO Mice Plaque vs. Normal Wall 0 5 10 15 Atherosclerotic Aorta Average number of iron particles per sample P <0.001
  • 24. MR Image of Abdominal Aorta After SPIO Injection in ApoE and Control Mice ApoE deficien t mouse C57B1 (control) mouse Before Injection After Injection (5 Days ) Dark (negatively enhanced) aortic wall, full of iron particles Bright aortic lumen and wall without negative enhancement and no significant number of iron particles
  • 25. Injection of Cytokine Increases SPIO-Loaded Macrophage Density in Aortic Plaques (Apo E Deficient Mice) Naghavi et al Circulation 2003
  • 26. Naghavi et al Circulation 2003 Injection of Cytokine Increases SPIO-Loaded Macrophage Density in a Coronary Plaque (Apo E Deficient Mice)
  • 27. Histopathologic studies of Thoracic aorta in Watanabe Hereditary Hypercholesterolemic rabbit after SPIO injection H&E staining Iron staining Iron staining
  • 28. Histopathologic studies of Thoracic aorta in Watanabe Hereditary Hypercholesterolemic rabbit after SPIO injection H&E staining Iron staining Iron staining Iron particles
  • 29. Plaque Cell Density vs SPIO 0 10 20 30 40 50 60 0 10 20 30 40 50 60 70 Cell Denity in H&E staining SPIOpositivecell-Iron staining Series1 R=0.956 Correlation between Iron positive cells in Iron staining and cell density in H&E staining in rabbit atherosclerotic aorta.
  • 30. MR Angiography 3D with Gadolinium-DTPA in Watanabe Rabbit Before SPIO injection After SPIO injection
  • 31. MRI Identifies Plaque Inflammation by SPIO Nanoparticles Watanabe rabbit Post-SPIO Watanabe rabbit control NZW rabbit control NZW rabbit Post-SPIO Watanabe Rabbit Post-SPIO Watanabe Rabbit Control NZW Rabbit Post-SPIO NZW Rabbit Control
  • 32. Ex-vivo MR study of the thoracic aorta in Watanabe and Wild type rabbit after SPIO injection compared to control. (Gradient echo) Watanabe rabbit Post-SPIO Watanabe rabbit control NZW rabbit Post-SPIO NZW rabbit control
  • 47. MR signal changes after CsA treatment. A group with allotransplants was treated with CsA for either 7 days (n=5) or 4 days (n=5) after initial MRI experiments showed decrease of MR signal intensity according to degree of graft rejection. On POD 14, transplanted rats were reinjected with USPIO particles, and then MRI experiments were performed. Animals treated 7 days showed minimal changes in MR signal intensity 24 hours after reinjection (A and B), and animals treated 4 days showed MR signal intensity that was significantly decreased after USPIO injection (C and D). MR images of short-axis view of graft are shown. MR images before USPIO infusion are at A and C, and images taken 24 hours after infusion are at B and D. Ho et al
  • 49. • Imaging Macrophage Activity in the Brain Using Ultrasmall Particles of Iron Oxide Jeff W.M. Bultea and Joseph A. Franka Laboratory of Diagnostic Radiology Research National Institutes of Health Bethesda, MD
  • 50.
  • 51. • SPIO MR imagine of macrophage is feasible for clinical applications. • It will be of great interest to investigate the cost-effectiveness of this technique in comparison with alternative diagnostic approaches. Conclusion
  • 52. • Poor spatial and temporal resolution for coronary applications • Cost • Cumbersome (injection and delayed imaging) Limitations