Radioactive Antibody Fragment May Help Scientists Identify Artery Deposits

Chicago, Illinois, UNITED STATES

Study Highlights:

  • Creating a tiny, radioactive antibody fragment may help scientists identify artery deposits most likely to burst and cause a heart attack.
  • A non-invasive system uses miniature antibodies to detect a molecule that identifies the vulnerable deposits.
  • Researchers plan clinical trials to determine the safety and efficacy of the new imaging technique.

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DALLAS, March 29, 2012 (GLOBE NEWSWIRE) -- Creating a radioactive antibody fragment may allow scientists to identify fat and debris deposits in artery walls that are most likely to rupture and cause heart attacks, according to a new study in Circulation: Research, an American Heart Association journal.

Of the more than 17 million annual cardiovascular deaths worldwide, most result from ruptured plaque.

"The detection of vulnerable coronary plaques is a major clinical challenge because it would allow preventive patient management prior to a heart attack," said Alexis Broisat, Ph.D., the study's lead author and a post-doctoral fellow at the University of Grenoble in France. "In clinical practice, there is currently no early, reliable and noninvasive tool allowing such detection."

The researchers created radioactive antibody fragments called nanobodies that attached to particles in artery plaque called vascular cell adhesion molecule-1 (VCAM1).

"Nanobodies constitute a promising new class of radiotracers for cardiovascular imaging," Broisat said.

Ongoing inflammation in a plaque deposit is a crucial sign that the plaque may rupture, and VCAM1 plays a major role in the inflammation process.

In laboratory tests, the radioactive nanobodies were attracted to VCAM-1.

In animal tests, researchers injected a solution containing the radioactive particles into the blood stream of mice with artery plaques. They then used a single-proton emission computed tomography (SPECT/CT) imaging scan to detect the radioactive particles.

The nanobodies attached to VCAM-1 expressing tissues. Following radiolabeling, some of the nanobodies remained stable in the laboratory and in mouse blood for six hours. This allowed imaging of the mice up to three hours after nanobody injection. These scans revealed plaques in the animals' aortic arches.

If approved for human use, physicians can inject nanobodies into patients to determine if they are at risk of plaque rupture.

"The early detection of trouble looming ahead could trigger steps for intervention, possibly involving the aggressive modulation of risk factors," according to an editorial accompanying the report by Matthias Nahrendorf, M.D., Ph.D., Jason R. McCarthy, Ph.D., and Peter Libby, M.D., of Harvard Medical School in Boston, Mass.

Before the imaging concept can be used regularly, researchers must conduct toxicology studies, produce clinical-quality material and determine whether the radiotracer technique is safe, beneficial and cost effective.

Broisat and his colleagues are planning clinical studies of the radiotracer technique to address these issues, including whether the anti-VCAM1 nanobodies can trigger adverse immune system reactions in people.

Broisat's co-authors are: Sophie Hernot, Ph.D.; Jakub Toczek, M.Sc.; Jens De Vos, M.Sc.; Laurent M. Riou, Ph.D.; Sandrine Martin, Ph.D.; Mitra Ahmadi, Ph.D.; Nicole Thielens, Ph.D.; Ulrich Wernery, Ph.D.; Vicky Caveliers, Ph.D.; Serge Muyldermans, Ph.D.; Tony Lahoutte, M.D., Ph.D.; Daniel Fagret, M.D., Ph.D.; Catherine Ghezzi, Ph.D.; and Nick Devoogdt, Ph.D.

Author disclosures and funding sources are on the manuscript.

Statements and conclusions of study authors published in American Heart Association scientific journals are solely those of the study authors and do not necessarily reflect the association's policy or position. The association makes no representation or guarantee as to their accuracy or reliability. The association receives funding primarily from individuals; foundations and corporations (including pharmaceutical, device manufacturers and other companies) also make donations and fund specific association programs and events. The association has strict policies to prevent these relationships from influencing the science content. Revenues from pharmaceutical and device corporations are available at

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NR12 – 1053 (Circ Res/Broisat) 

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