| Literature DB >> 31123149 |
Cuihua Wang1, Edmund Keliher1, Matthias W G Zeller1, Gregory R Wojtkiewicz1, Aaron D Aguirre1,2, Leonard Buckbinder3, Hye-Yeong Kim1, Jianqing Chen3, Kevin Maresca3, Maaz S Ahmed1, Negin Jalali Motlagh1, Matthias Nahrendorf1, John W Chen4,5.
Abstract
Myeloperoxidase (MPO) is a critical proinflammatory enzyme implicated in cardiovascular, neurological, and rheumatological diseases. Emerging therapies targeting inflammation have raised interest in tracking MPO activity in patients. We describe 18F-MAPP, an activatable MPO activity radioprobe for positron emission tomography (PET) imaging. The activated radioprobe binds to proteins and accumulates at sites of MPO activity. The radioprobe 18F-MAPP has a short blood half-life, remains stable in plasma, does not demonstrate cytotoxicity, and crosses the intact blood-brain barrier. The 18F-MAPP imaging detected sites of elevated MPO activity in living mice embedded with human MPO and in mice induced with chemical inflammation or myocardial infarction. The 18F-MAPP PET imaging noninvasively differentiated varying amounts of MPO activity, competitive inhibition, and MPO deficiency in living animals, confirming specificity and showing that the radioprobe can quantify changes in in vivo MPO activity. The radiosynthesis has been optimized and automated, an important step in translation. These data indicate that 18F-MAPP is a promising translational candidate to noninvasively monitor MPO activity and inflammation in patients.Entities:
Keywords: PET imaging; inflammation; myeloperoxidase
Year: 2019 PMID: 31123149 PMCID: PMC6575581 DOI: 10.1073/pnas.1818434116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205