June 8, 2015
Molecular imaging tracks an immune response tied to neurodegenerative disease
Baltimore, Md. (Embargoed until 12:30 pm EDT on Monday, June 8) – Neuroinflammation caused by a reactive immune system could be tripping off the neurodegeneration seen in certain dementias, multiple sclerosis, and other deadly diseases of the nervous system. A novel molecular imaging technique could be the key to understanding how best to treat these and other devastating diseases, according to a recent study presented at the 2015 Annual Meeting of the Society of Nuclear Medicine and Molecular Imaging (SNMMI).
At the heart of this maladaptive immune response are microglia, immune cells in the central nervous system that can be activated to trigger neuroinflammation. For this study, researchers used positron emission tomography (PET) to measure activation of microglia by employing a molecule from E. coli bacteria called lipopolysaccharide (LPS), or endotoxin. LPS stimulates the immune system and is accompanied by a radiotracer called carbon-11 PBR28 (C-11 PBR28). This form of molecular imaging allows the minimally invasive visualization of neuroinflammation. C-11 PBR28, is injected and binds to translocator proteins expressed on activated microglia. A PET scanner can then detect the radioactive particles emitted from inside the brain, representing areas of increased microglial activation before and after immune stimulation with LPS.
“The imaging technique could shed light on the immune dysfunction that underpins a broad range of neuroinflammatory diseases, such as Alzheimer’s disease, depression, post-traumatic stress disorder and addiction,” said Christine Sandiego, PhD, lead author of the study and a researcher from the department of psychiatry at the Yale School of Medicine in New Haven, Conn. “This is the first human study that accurately measures this immune response in the brain. The discoveries made with this technique could contribute to promising new drug treatments.”
The PET radiotracer C-11 PBR28 was administered to eight healthy men around the age of 25, give or take six years, followed by two separate PET scans on the same day for each subject before and after injection with LPS. Adverse symptoms were self-reported and blood samples were taken to assess levels of peripheral inflammation. Results of the study showed that administering LPS led to a substantial spike in the systemic inflammatory response and levels of reported sickness, and activated microglia in the central nervous system.
With further research, eventual drug therapies could potentially cut the activation of neurodegenerative microglia and encourage neuroprotective processes in the brain.
Scientific Paper 468:“Systemic endotoxin induces a robust increase in microglial activation measured with [11C]PBR28 and PET in humans,” C.M. Sandiego, K. Cosgrove, Psychiatry, Yale University, New Haven, Connecticut; J. Gallezot, K. Lim, S. Lin, Y. Huang, R.E. Carson, Diagnostic Radiology, Yale University, New Haven, Conn.; L. Devine, Laboratory Medicine, Yale University, New Haven, Conn.; K. O'Connor, Neurology, Yale University, New Haven, Conn.; J. Hannestad, Neurosciences, UCB Pharma SA, Braine-l’Alleud, Belgium; SNMMI’s 62nd Annual Meeting, June 6–10, 2015, Baltimore, Md.
About the Society of Nuclear Medicine and Molecular Imaging
The Society of Nuclear Medicine and Molecular Imaging (SNMMI) is an international scientific and medical organization dedicated to raising public awareness about nuclear medicine and molecular imaging, a vital element of today’s medical practice that adds an additional dimension to diagnosis, changing the way common and devastating diseases are understood and treated and helping provide patients with the best health care possible.
SNMMI’s 18,000 members set the standard for molecular imaging and nuclear medicine practice by creating guidelines, sharing information through journals and meetings and leading advocacy on key issues that affect molecular imaging and therapy research and practice. For more information, visit www.snmmi.org.