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The rapidly evolving field of molecular imaging promises important advances in the diagnosis, characterization and pharmacological treatment of vascular disease. Magnetic resonance imaging (MRI) provides a modality that is well suited to vascular imaging as it can provide anatomical, structural and functional data on the arterial wall. Its capabilities are further enhanced by the use of a range of increasingly sophisticated contrast agents that target specific molecules, cells and biological processes. This article will discuss one such approach, using microparticles of iron oxide (MPIO).
MPIO have been shown to create highly conspicuous contrast effects on T2*-weighted MR images. We have developed a range of novel ligand-conjugated MPIO for molecular MRI of endothelial adhesion molecules, such as vascular cell adhesion molecule-1 (VCAM-1) and P-selectin expressed in vascular inflammation, as well as activated platelet thrombosis. This review discusses the application of ligand-targeted MPIO for in vivo molecular MRI in a diverse range of vascular disease models including acute vascular inflammation, atherosclerosis, thrombosis, ischemia-reperfusion injury and ischemic stroke. The exceptionally conspicuous contrast effects of ligand-conjugated MPIO provide a versatile and sensitive tool for quantitative vascular molecular imaging that could refine diagnosis and measure response to treatment. The potential for clinical translation of this new class of molecular contrast agent for clinical imaging of vascular syndromes is discussed.
In clinical practice, the early identification and characterization of atherosclerotic lesions at risk of progressing to cause myocardial infarction (MI) and ischemic stroke remains challenging. X-ray arteriography is the standard clinical imaging technique used to estimate the degree of luminal stenosis, but detects only the silhouette of the vessel wall against the lumen and does not provide information on plaque composition. More sophisticated non-invasive imaging techniques are required that can accelerate and refine diagnosis, guide intervention and monitor response to therapies that may stabilize lesions and prevent future atherothrombotic events .
Molecular imaging is a rapidly evolving field, which presents opportunities to shift emphasis from imaging plaque structure to reporting directly the biological processes of vascular disease at the molecular and cellular levels . Specific targeting of molecules is achieved through the development of purpose-built molecular imaging probes, usually consisting of a contrast agent conjugated to specific targeting ligands . Advances in nanotechnology have led to the development of an array of nano- and micrometer-sized particle contrast agents for application in molecular imaging. The most successful approaches have involved the development of molecular imaging agents that can deliver substantial payloads of paramagnetic gadolinium (Gd) chelates or superparamagnetic iron oxide to a specific molecular target (Fig. 1). Functionalization of the particle surface with reactive surface groups enables covalent conjugation of a variety of targeting ligands including antibodies, peptides, aptamers and small molecule peptidomimetics to the particle surface.
In atherosclerosis, a diverse range of molecular targets are expressed both at the endothelial surface and by cells within the vessel wall of the artery. Importantly, there is differential expression of some of these targets from early lesion formation to advanced vulnerable plaques and thrombotic complications [1,3,4]. For instance, early markers of atherogenesis include endothelial cell adhesion molecules, such as P- and E-selectin, vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1), which facilitate mononuclear leukocyte recruitment to activated endothelium and subsequent transmigration into the subendothelial space [5–7]. Molecular imaging of endothelial adhesion molecules has been at the forefront of this field, since the upregulation of these molecules is an early event in a broad range of vascular diseases including atherosclerosis, ischemia-reperfusion injury, ischemic stroke and cancer. Furthermore, their endothelial location makes them accessible to blood-borne contrast agents. However, one of the challenges for molecular imaging of endovascular targets is to deliver targeted contrast agents in sufficient density to detect molecular expression of relatively low-abundance targets confined to a two-dimensional endothelial monolayer and to achieve this under high physiological shear stresses.
Shapiro et al. showed that microparticles of iron oxide (MPIO) provide excellent contrast effects . In this paper, we will focus on the application of ligand-targeted MPIO for molecular MRI of endothelial adhesion molecules in experimental models of acute vascular inflammation , ischemia-reperfusion injury , atherosclerosis  and ischemic stroke . We also highlight a similar ligand-targeted MPIO strategy for MRI detection of activated platelet thrombosis. Finally, we discuss the scope for application of ligand-targeted MPIO in clinical imaging of vascular syndromes.
A range of imaging techniques are currently used to image atherosclerosis including intravascular ultrasound (IVUS), multiple-row detector computed tomography (MDCT), positron emission tomography (PET), MRI and optimal coherence tomography (OCT) . Of these only nuclear techniques have proven record in clinical molecular imaging. PET can assess atherosclerotic inflammatory plaque activity using exogenously administered 18Fluorine preparations, such as 2-[18F]fluoro-2-deoxy-d-glucose (FDG). This glucose analogue accumulates in metabolically active tissue, yielding a signal that is proportional to glycolytic activity. It has been shown that inflamed, metabolically active, plaques may be detectable by 18FDG-PET. Rudd et al. demonstrated the ability of 18FDG-PET imaging to highlight inflammatory activity in unstable carotid plaques in patients undergoing carotid endarterectomy, relative to the contralateral asymptomatic artery . 18FDG was taken up by atherosclerotic plaque and selectively accumulated in macrophage-rich areas. Indeed, the first investigations of treatment effects of on plaque activity are beginning to emerge . The advantages of PET are related to its extreme sensitivity and quantitative outputs. Opportunities to apply PET in the evaluation of atherosclerosis and its treatment should extend beyond macrophage imaging through the development of novel ‘radio-ligands’. For example, the development of imaging probes that target matrix metalloproteinases , serine proteases  and apoptosis [18–20], could allow the visualization of response to treatment in ‘high risk’ plaques. While PET has much higher detection sensitivity (picomolar range) than MRI, and much better tissue penetration than ultrasound or OCT, the disadvantages of PET are its limited spatial resolution, logistics of isotope provision, substantial radiation exposure and expense.
MRI has emerged as a leading non-invasive imaging modality for assessing vascular pathologies, due to its excellent spatial resolution (sub-millimeter) and soft tissue contrast and high signal to noise ratio. Using multi-contrast sequences, MRI can differentiate atherosclerotic plaque composition, based on differences in biophysical and biochemical properties such as chemical composition and concentration, water content, physical state, molecular motion or diffusion . High resolution MRI can also accurately quantify plaque components such as fibrous cap thickness and size of the lipid core [21,22]. Since MRI does not involve ionizing radiation, serial imaging can be performed safely over time within the same patient. Furthermore, intravenous Gd-based or iron oxide-based MRI contrast agents can be used to improve image sensitivity to enhance differences between healthy and diseased vessels.
Gd chelates, such as gadolinium diethylene-triamine-penta-acetic acid (Gd-DTPA), provide positive signal enhancement on T1 weighted MR images due to their effects on shortening water proton T1 relaxation times. However, Gd chelates have inherently low sensitivity (micromolar range). For molecular imaging, a number of strategies have been employed to amplify the Gd contrast effects and to deliver sufficient quantities of Gd in vivo in order to detect biological activity of lesions. A range of nanoparticles carrying substantial payloads of amphipathic Gd chelates embedded in their outer membrane have been constructed, including liposomes , perfluorocarbon lipid emulsions  and micelles [25,26]. Lipoprotein micelles enriched with hydrophobic Gd chelates have also been developed for the detection of macrophages within atherosclerotic plaques [27–29]. However, the relaxivity effects achievable are relatively modest, compared to superparamagnetic particles of iron oxide (SPIO) [27,30]. A further potential disadvantage of hydrophobic Gd chelates is the recently observed severe long-term toxicity effects (including nephrogenic sclerosing fibrosis: NSF) in patients with impaired renal function . However, it may be the case that targeted contrast agents could be used at lower total Gd-dose, reducing the potential for this type of toxicity.
Superparamagnetic iron oxide-based agents consist of a core of iron oxides, surrounded by a dextran or polymer coat. Iron oxide agents, shorten T2 and T2* relaxation times, creating hypointense areas that appear black on the MR image on T2- and T2*-weighted MR images. Iron oxide agents include ultrasmall superparamagnetic particles of iron oxide (USPIO) (20–50 nm diameter), superparamagnetic particles of iron oxide (SPIO) (60 to approximately 250 nm) and micrometer-sized particles of iron oxide (MPIO) (0.9–8 μm). Iron oxide agents have superior sensitivity in MR contrast, compared to Gd [32,33]. In particular, MPIO convey a payload of iron oxide (typically 0.1–1.6 pg iron/MPIO particle), which is orders of magnitude greater than that contained in nanometer-sized particles . The effects of MPIO on local magnetic field homogeneity and detectable contrast extend a distance up to 50 times the physical diameter of the microparticle, known as a contrast “blooming effect” . MPIO have been shown to be useful for cellular MRI, enabling in vivo detection of single cells  and cell tracking  using only a small number of MPIO.
For molecular imaging of endovascular targets, MPIO offer a number of important attributes. First, the relatively large size and incompressible nature of MPIO, makes them less susceptible to non-specific vascular egress or uptake by endothelial cells than nanometer-sized particles , thus they can retain specificity for endothelial molecular targets. Secondly, unbound MPIO have been shown to clear rapidly from the blood (blood half-life <2 min in rats), thus minimising background blood phase contrast . Conversely, USPIO have a long blood half-life (up to 24 h), which for MRI of endothelial molecular targets, may cause high background contrast for an extended period, making it difficult to distinguish specific contrast effects from normal tissue heterogeneity and other susceptibility artefacts. However, “positive” contrast MRI sequences are being developed to generate MR signal enhancement from regions containing iron oxide particles [38,39]. Thirdly, due to the contrast “blooming effect” of MPIO, a small number of MPIO can create potent hypointense contrast effects on T2*-weighted images, thereby greatly enhancing sensitivity, especially for low-abundance endothelial molecular targets. MPIO contrast effects may be readily distinguished on T2*-weighted images using in vivo gradient-echo MRI. MPIO have been demonstrated to provide a platform for quantitative molecular imaging of vascular endothelial targets, whereby the extent of contrast effects may directly report specific molecular endothelial expression [9–11].
Recently, SPIO with optimised high relaxation properties have been developed for quantitative in vivo MRI of lipoprotein metabolism  and ultra-sensitive detection of bacteria . Cormode et al. have demonstrated that iron oxide nanocrystals can be used instead of Gd to label high density lipoprotein (HDL) particles for molecular imaging of macrophage expression in atherosclerosis . Whilst effective for the applications reported, the small size of these particles is likely to be limiting to their application in molecular endothelial imaging, where the delivery of sufficient contrast volume is challenging, on the ‘planar’ target that is on the surface of the blood vessel wall.
The targeting of MPIO to specific molecules may be accomplished by the conjugation of ligands to functional groups on the surface of the microparticle. MPIO are commercially available with a variety of reactive surface groups including carboxylic acid, amine and p-toluene sulphydryl (tosyl) groups. These functionalized MPIO offer opportunities to covalently conjugate a range of targeting ligands including monoclonal antibodies or their immunospecific fragments F(ab), aptamers or small peptides generated by phage display or small molecule screens. Phage display provides a powerful method for the production of novel antibody or peptide ligands from libraries of bacteriophage (viruses that infect bacterial cells) using standard recombinant DNA technology. Functionalized MPIO therefore provide a versatile platform that can be readily adapted for molecular imaging of a variety of endovascular molecular targets in experimental, pre-clinical investigations of vascular inflammatory diseases. In Table 1, applications of targeted and non-targeted MPIO for molecular and cellular imaging of vascular syndromes are listed.
We have applied tosyl-activated MPIO for direct covalent conjugation of monoclonal antibodies directed against vascular endothelial adhesion molecules, including P-selectin and VCAM-1, which are involved in leukocyte recruitment during early vascular inflammation. Below, we review the application of tosyl-activated MPIO for in vivo molecular MRI detection of vascular endothelial adhesion molecule upregulation in diverse models of clinically important vascular pathologies including acute vascular inflammation , atherosclerosis , ischemia-reperfusion injury  and ischemic stroke . We also highlight the application of similar cobalt-functionalized MPIO for direct covalent conjugation to histidine (His) tagged single-chain antibodies, targeted towards activated platelets in mouse models of atherothrombosis [43,44]. Finally, we discuss the potential clinical translation of ligand-targeted MPIO as a versatile adjunct in the clinical imaging arena.
Acute inflammation of the central nervous system (CNS) is associated with enhanced expression of endothelial adhesion molecules. Endothelial VCAM-1 and its ligand, α4β1 integrin (also called very late antigen-4, VLA-4) are key mediators of leukocyte recruitment and lesion development . VCAM-1 is not constitutively expressed on the vascular endothelium but is up-regulated upon endothelial activation . Furthermore, selective VCAM-1 inhibitors such as natalizumab that bind to the α4 subunit of α4β1 integrin are effective anti-inflammatory agents, for instance in the treatment of multiple sclerosis . For these reasons, VCAM-1 is an attractive molecular imaging target of acute vascular inflammation.
VCAM-1 targeted MPIO can conspicuously show upregulation of VCAM-1 in a mouse model of early cerebral inflammation by molecular in vivo MRI, at a time when pathology is otherwise undetectable by conventional imaging techniques . MPIO (1 μm diameter), with reactive tosyl groups, were covalently conjugated to mouse monoclonal antibodies against VCAM-1 (VCAM-MPIO) or IgG isotype negative control. The capacity of VCAM-MPIO constructs for specific and quantitative binding was tested in vitro using a mouse endothelial cell line (sEND-1), stimulated with graded doses of tumor necrosis factor-α (TNF-α). Differential interference confocal microscopy showed a TNF-α dose-dependent increase in VCAM-MPIO binding, which co-localized with VCAM-1 immunofluorescence on the endothelial cell surface. Furthermore, VCAM-MPIO binding to stimulated cells was inhibited when the VCAM-MPIO were pre-incubated with soluble decoy VCAM-1 (mouse recombinant Fc-VCAM-1) (Fig. 2A).
For in vivo experiments, pro-inflammatory interleukin 1β (IL-1β) was stereotactically injected into the left corpus striatum of NMRI mice to induce acute vascular inflammation. The contralateral hemisphere received no injection and served as an internal control. VCAM-MPIO or negative control IgG-MPIO (~4.5 mg/kg body weight) were intravenously injected 3 h after IL-1β injection and allowed to circulate for 1.5–2 h prior to MRI. To block VCAM-1 binding sites, a further group of mice were pre-treated with VCAM-1 antibody 3 h after IL-1β injection and VCAM-MPIO administered 15 min later. In vivo MRI was performed at 7 T using a T2*-weighted 3D gradient-echo sequence (acquisition ~1 h; isotropic resolution 88 μm3). VCAM-MPIO produced highly specific hypointense signal areas in the IL-1β activated hemisphere, which delineated the architecture of activated cerebral blood vessels, with minimal contrast effects in the contralateral, unstimulated hemisphere (Fig. 2B and C). Mice that received negative control IgG-MPIO and mice pre-treated with VCAM-1 antibody prior to VCAM-MPIO injection also showed minimal contrast effects. The specificity and potency of VCAM-MPIO contrast effects were derived from a combination of targeted delivery of MPIO containing a large amount of iron oxide to sites of early inflammation and rapid clearance of MPIO from the blood which minimizes background signal. Previously, Gd-based nanoparticles conjugated to Sialyl Lewisx (sLeX) mimetic moiety (Gd-DTPA-sLexA) have been reported to detect early endothelial activation of E-selectin in a rat model of brain inflammation . Detection of ICAM-1 upregulation has also been reported by ex vivo MRI (9.4 T) using antibody-conjugated paramagnetic liposomes .
In the application described above, MPIO accumulate in cerebral venules, where shear stresses and flow rates are relatively low. Atherosclerosis, however, is characterized by the accumulation of lipid-rich, fibrous and cellular elements within the wall of large and medium-sized arteries, including the coronary and carotid arteries, as well as the aorta and peripheral vessels [50–52]. Molecular imaging of the vascular endothelium of large arteries presents challenges since the contrast agent has to bind in sufficient density to a two-dimensional monolayer exposed to high physiological shear stress conditions. The dynamics of leukocyte binding to activated endothelium are complex and rely on multiple receptor-ligand interactions. Initial leukocyte rolling is mediated by E- and P-selectin whereas firm adhesion to the vascular wall is mediated via integrin binding with intercellular adhesion molecule-1 (ICAM-1) and VCAM-1, with the latter more important in initiation of atherosclerosis [6,53]. VCAM-1 is not constitutively expressed but is upregulated at atherosclerosis-prone sites even before macroscopic disease is apparent, with persistent expression in more advanced atherosclerotic lesions [54,55]. Computed models of adhesion molecule dynamics predict synergistic roles for selectins and integrins with transition between rolling and firm adhesion dependent on the binding affinities and relative concentrations of receptor-ligand interactions [56,57].
In order to mimic the in vivo multi-step dynamics of leukocyte adhesion, we have constructed dual antibody-conjugated MPIO (4.5 μm diameter) using monoclonal antibodies to P-selectin and VCAM-1, in a 50:50 combination (PV-MPIO) . As predicted by computed models, we have demonstrated using in vivo bioassays that dual-targeted MPIO markedly enhance binding to atherosclerotic plaque endothelium compared to single-ligand MPIO (7-fold increase in binding compared with P-selectin-MPIO and 6-fold increase compared with VCAM-MPIO) (Fig. 3A) . The ability of dual-ligand PV-MPIO to bind to aortic root plaque endothelium in vivo was then investigated using apo E−/− mice, fed a high fat diet for 26 weeks. Apo E−/− mice were intravenously injected with dual-targeted PV-MPIO or negative control IgG-MPIO (30 mg iron per kg body weight) and allowed to circulate for 30 min. Mice were terminally anesthetized and the arterial tree perfusion fixed and embedded in an MR tube for high resolution ex vivo MRI (9.4 T). MPIO binding was readily distinguished on the arterial endothelium of plaque, providing excellent visualization by MRI (Fig. 3C). 3D reconstruction of segmented images demonstrated specific PV-MPIO binding localized to atherosclerotic plaque endothelium throughout the aortic root, with minimal retention of IgG-MPIO (Fig. 3D). No MPIO binding was observed in atherosclerosis-free areas of the ascending aorta.
We had purposely used relatively large MPIO (4.5 μm diameter) to target endothelial adhesion molecule expression in aortic atherosclerotic plaques because of their presumed superior contrast effects . However, the dual-ligand conjugation protocol could be applied to smaller 1 μm diameter MPIO, which we now appreciate may be less buoyant in the circulation that these larger MPIO and therefore may exhibit effective contrast binding at lower doses. Similar dual-targeted microbubbles conjugated with Sialyl Lewisx and ICAM-1 antibody have also been developed for molecular ultrasound imaging, although in that case, binding efficiency was increased only marginally by the combination. We speculate that this was due to stearic limitations resulting from the size mismatch of the glycoprotein and antibody ligands . Several iron oxide nanoparticle agents conjugated to novel VCAM-1 internalising peptides, identified by phage display have also been reported. These peptides bind specifically to activated endothelium and are internalized by cells expressing VCAM-1, allowing progressive concentration by endothelial cells [59,60].
Vascular inflammation is a key feature following ischemia-reperfusion injury (IRI)  in acute vascular syndromes such as myocardial infarction [62–64], stroke [65,66], cardiac surgery  and organ transplantation . The upregulation of endothelial adhesion molecule expression persists after the ischemic event itself has resolved and therefore may provide a functional imprint of a prior ischemic insult . We have recently shown that VCAM-MPIO (1 μm diameter) can detect VCAM-1 expression in a mouse model of unilateral renal IRI [10,70]. We also identified in vitro using TNF-α stimulated cells that VCAM-MPIO binding correlates with both VCAM-1 protein and mRNA levels, as determined by western blotting and RT-PCR respectively . For in vivo studies, IRI was induced in male C57BL/6 mice by clamping the left renal pedicle for 30 min, while the contralateral pedicle was exposed but not instrumented . After 16–18 h reperfusion, mice were intravenously injected with VCAM-MPIO or irrelevant control IgG-MPIO (4.5 mg iron per kg). A further group of mice were pre-treated with VCAM-1 antibody 15 min prior to VCAM-MPIO injection to block VCAM-1 binding sites. In vivo MRI (9.4 T) was performed for 90 min post-contrast injection using a double-gated 3D gradient-echo sequence, optimized to provide both bright blood and T2*-weighted contrast (resolution 100 μm3). Significant VCAM-MPIO binding was observed in both the medulla and cortex of IRI kidneys compared with irrelevant control IgG-MPIO. Pre-treatment of mice with VCAM-1 antibody prior to VCAM-MPIO administration abolished retention of VCAM-MPIO.
Recently, Hoyte et al. have demonstrated that VCAM-MPIO can detect unilateral cerebral ischemia in a mouse model of experimental stroke . Barber et al. have also reported molecular MRI of transient middle cerebral artery brain ischemia using Gd-DTPA-sLexA, targeting both P- and E-selectin, but identified limitations in contrast sensitivity . Targeted ultrasound microbubbles, targeting P-selectin and ICAM-1 have been developed and applied to image mouse renal [73,74] and myocardial IRI [75,76]. Current clinical imaging techniques are hampered by an inability to define the extent and distribution of ischemia in acute vascular syndromes. The ability of our ligand-targeted MPIO approach to depict the volume of endothelial inflammation following IRI, in relation to the vasculature, may aid accelerated diagnosis of parenchymal ischemia and potentially, guide targeted interventions.
Activated platelets are known to be involved both in the initiation of atherosclerosis and in advanced atherosclerotic events, such as plaque rupture and thrombus formation [77,78,79]. The platelet-specific glycoprotein GP IIb/IIIa receptor (CD41/CD61, also known as αIIbβ3 integrin) mediates the final common pathway of platelet aggregation via fibrinogen and is key to thrombus formation . Recently, a single-chain antibody that specifically recognizes ligand-induced binding sites (LIBS) on GP IIb/IIIa receptors, which become exposed only upon activation by receptor-ligand binding, has been developed [81–83] The LIBS antibody has been shown to bind only to activated platelets, e.g. when adherent to damaged endothelium, and does not to bind to non-activated circulating platelets. von zur Muhlen et al. recently applied cobalt-functionalized MPIO (1 μm diameter) conjugated to the histidine tag of LIBS single-chain antibodies (LIBS-MPIO) for the detection of activated platelets in a mouse model of endovascular platelet aggregation using ex vivo MRI (11.7 T) (Fig. 4A) . LIBS-MPIO agent have also been applied in a mouse model of wall-adherent, carotid thrombosis for the detection of platelet-rich thrombi by in vivo MRI (Fig. 4C) . LIBS-MPIO reliably tracked a reduction in thrombus size in response to pharmacological thrombolysis treatment with urokinase (Fig. 4D). LIBS-MPIO have also been used to detect human platelet aggregates in explanted symptomatic carotid artery plaque specimens by ex vivo MRI (9.4 T)  and human platelet-rich clots in vitro using clinically relevant magnetic field strengths (3 T) .
For clinical purposes, the commercial MPIO that we have used are non-biodegradable, due to their polyurethane coat, and are not suitable for human applications. However, for clinical translation, it should be feasible to synthesize biodegradable MPIO with suitable modification of the surface coat, similar to the iron oxide containing contrast media that are already in clinical use . In fact, the development of biodegradable MPIO suitable for clinical use is already underway [86–89]. Our ligand-targeted MPIO approach has focused on the use of monoclonal antibodies. Potential immunogenicity can be attenuated by the use of modified or “humanized” antibodies  and single-chain antibodies [43,82]. However, antibody production on a scale required for clinical application is also relatively complex and expensive. Sugar-based ligands, such as sLeX, have recently been applied to develop novel glyconanoparticles , and may prove useful ligands for clinical application.
For our in vivo imaging studies, the dose of iron that we have used (4.5 mg iron/kg body weight) has been well tolerated, with no animals showing any short-term ill effects. This iron dose closely reflects the dose of USPIO (2.6 mg iron/kg body weight) used extensively for human oncological MRI . Further dose-ranging studies will determine whether the iron dose can be reduced further. Importantly, MPIO, which are considerably smaller than red blood cells (Fig. 5A), do not induce any evidence of hemorrhage or tissue infarction due to small vessel ‘plugging’  and are rapidly sequestered by the liver and spleen (Fig. 5B) . Another important advantage of the MPIO approach is the ability to relate specific MPIO binding to the blood vessel architecture . The anatomical distribution together with the degree and timing of contrast binding may add further functional specificity for vascular pathological processes under evaluation.
In summary, we have developed a new approach to molecular imaging of endovascular targets using ligand-conjugated MPIO, which we have applied in a diverse range of vascular syndromes including acute brain inflammation, atherosclerosis, renal ischemia-reperfusion injury, ischemic stroke and thrombus formation. The versatility of functionalized MPIO and the potency of the contrast effects in detecting relatively low-abundance endothelial molecular targets, offers a potentially valuable platform for accelerating diagnosis and guiding specific treatment of vascular inflammatory diseases.
This work was funded by The Wellcome Trust and the British Heart Foundation. Dr. Choudhury's laboratory is also supported by the Oxford Comprehensive Biomedical Research Centre, NIHR funding scheme.
Based on the John French Lecture given by Dr. Robin Choudhury at the British Atherosclerosis Society and British Society for Cardiovascular Research joint spring meeting, Oxford, UK, April 2–3, 2009.