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New pathogen-specific immunoPET/MR tracer for molecular imaging of a systemic bacterial infection

The specific and rapid detection of Enterobacteriaceae, the most frequent cause of gram-negative bacterial infections in humans, remains a major challenge. We developed a non-invasive method to rapidly detect systemic Yersinia enterocolitica infections using immunoPET (antibody-targeted positron emi...

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Detalles Bibliográficos
Autores principales: Wiehr, Stefan, Warnke, Philipp, Rolle, Anna-Maria, Schütz, Monika, Oberhettinger, Philipp, Kohlhofer, Ursula, Quintanilla-Martinez, Leticia, Maurer, Andreas, Thornton, Christopher, Boschetti, Frederic, Reischl, Gerald, Autenrieth, Ingo B., Pichler, Bernd J., Autenrieth, Stella E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905453/
https://www.ncbi.nlm.nih.gov/pubmed/26934329
http://dx.doi.org/10.18632/oncotarget.7770
Descripción
Sumario:The specific and rapid detection of Enterobacteriaceae, the most frequent cause of gram-negative bacterial infections in humans, remains a major challenge. We developed a non-invasive method to rapidly detect systemic Yersinia enterocolitica infections using immunoPET (antibody-targeted positron emission tomography) with [(64)Cu]NODAGA-labeled Yersinia-specific polyclonal antibodies targeting the outer membrane protein YadA. In contrast to the tracer [(18)F]FDG, [(64)Cu]NODAGA-YadA uptake co-localized in a dose dependent manner with bacterial lesions of Yersinia-infected mice, as detected by magnetic resonance (MR) imaging. This was accompanied by elevated uptake of [(64)Cu]NODAGA-YadA in infected tissues, in ex vivo biodistribution studies, whereas reduced uptake was observed following blocking with unlabeled anti-YadA antibody. We show, for the first time, a bacteria-specific, antibody-based, in vivo imaging method for the diagnosis of a Gram-negative enterobacterial infection as a proof of concept, which may provide new insights into pathogen-host interactions.