Inflammatory Cell Trafficking After Myocardial Infarction

University of Edinburgh

Status: Withdrawn

Conditions: Inflammation; Myocardial Infarction

Treatments: Other: Cardiac magnetic resonance imaging; Other: Infusion of investigational product

Study type: Interventional

Funder types: Other

Identifiers

NCT01127113

EDO001

Details and patient eligibility

About

Myocardial infarction (heart attack) is usually the consequence of rupture of a fatty 'plaque' in a heart artery. The presence of this fat and debris causes the propagation of a blood clot and blockage of the artery. The heart muscle normally supplied by the artery becomes deprived of oxygen and, if starved for long enough, this area of muscle dies. Much of the heart muscle damage is caused by overactivation of inflammatory cells. Whilst inflammation can be beneficial in healing processes, there is accumulating evidence that overactivation of inflammatory processes contributes to further muscle damage and cell death during myocardial infarction. We have recently developed a means of labelling human blood cells with 'nanoparticles' of iron oxide which can then safely be reinjected into the blood to allow the cells to be tracked and seen in the body using a conventional magnetic resonance scanner.

In the proposed study we aim to recruit patients with recent heart attacks to perform similar cell labelling and reinjection of labelled cells into the same volunteer's blood stream via the arm to track the fate of the blood cells over the course of days to months. We think that the labelled inflammatory cells will 'home' to the site of the heart attack and will be visible using magnetic resonance imaging (MRI) of the heart. We aim not only to highlight the role of inflammatory cells in myocardial infarction, but also propose that, if successful, this technique could be used in the future to assess the effects of antiinflammatory treatments currently being developed for the treatment of patients with heart attacks. The technique could also be extended to allow labelling of other cell types, including stem cells, to let us further understand how these cells may contribute to repair of damaged organs including the heart.

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Presentation with acute ST segment elevation myocardial infarction:

  • 1 mm ST elevation in at least two contiguous limb leads, or
  • 2 mm ST elevation in at least two contiguous praecordial leads, or new onset bundle branch block

• Successful treatment with primary percutaneous coronary intervention Restoration of TIMI grade 3 flow in infarct-related artery

• Troponin I ≥10 IU/mL at 12 hours after the onset of chest pain

• Age 18 - 80 years

Exclusion criteria

• Left main stem or severe multi-vessel coronary artery disease
• Continued symptoms of angina at rest or minimal exertion
• Atrial fibrillation
• Symptomatic heart failure; Killip Class ≥2.
• Hepatic or renal failure (estimated glomerular filtration rate <25 mL/min)
• Terminal illness or malignancy
• Anaemia
• Contraindication to magnetic resonance imaging
• Hepatitis B, hepatitis C, HTLV, HIV or syphilis infection
• Patients at risk of allergy to protamine (fish allergy, infertile men, previous vasectomy)

Trial design

Primary purpose: Basic Science

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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0 participants in 3 patient groups, including a placebo group

SPIO-labelled mononuclear cells

Active Comparator group

Treatment:

Other: Infusion of investigational product

Other: Cardiac magnetic resonance imaging

Unlabelled mononuclear cells

Placebo Comparator group

Treatment:

Other: Infusion of investigational product

Other: Cardiac magnetic resonance imaging

SPIO alone

Active Comparator group

Treatment:

Other: Infusion of investigational product

Other: Cardiac magnetic resonance imaging