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Selective depletion of radiolabeled HER2-specific antibody for contrast improvement during PET

The prolonged in vivo persistence of antibodies results in high background and poor contrast during their use as molecular imaging agents for positron emission tomography (PET). We have recently described a class of engineered Fc fusion proteins that selectively deplete antigen-specific antibodies w...

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Detalles Bibliográficos
Autores principales: Khare, Priyanka, Sun, Wei, Ramakrishnan, Sreevidhya, Swiercz, Rafal, Hao, Guiyang, Lo, Su-Tang, Nham, Kien, Sun, Xiankai, Ober, Raimund J., Ward, E. Sally
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489906/
https://www.ncbi.nlm.nih.gov/pubmed/34592895
http://dx.doi.org/10.1080/19420862.2021.1976705
Descripción
Sumario:The prolonged in vivo persistence of antibodies results in high background and poor contrast during their use as molecular imaging agents for positron emission tomography (PET). We have recently described a class of engineered Fc fusion proteins that selectively deplete antigen-specific antibodies without affecting the levels of antibodies of other specificities. Here, we demonstrate that these Fc fusions (called Seldegs, for selective degradation) can be used to clear circulating, radiolabeled HER2-specific antibody during diagnostic imaging of HER2-positive tumors in mice. The analyses show that Seldegs have considerable promise for the reduction of whole-body exposure to radiolabel and improvement of contrast during PET.