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Immune Checkpoint Inhibitor-Mediated Cancer Theranostics with Radiolabeled Anti-Granzyme B Peptide

Although immune checkpoint inhibitors (ICI) have revolutionized cancer management, patient response can be heterogeneous, and the development of ICI resistance is increasingly reported. Novel treatment strategies are necessary not only to expand the use of ICI to previously unresponsive tumor types...

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Detalles Bibliográficos
Autores principales: de Aguiar Ferreira, Carolina, Heidari, Pedram, Ataeinia, Bahar, Sinevici, Nicoleta, Granito, Alyssa, Kumar, Hritik Mahajan, Wehrenberg-Klee, Eric, Mahmood, Umar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9325142/
https://www.ncbi.nlm.nih.gov/pubmed/35890355
http://dx.doi.org/10.3390/pharmaceutics14071460
Descripción
Sumario:Although immune checkpoint inhibitors (ICI) have revolutionized cancer management, patient response can be heterogeneous, and the development of ICI resistance is increasingly reported. Novel treatment strategies are necessary not only to expand the use of ICI to previously unresponsive tumor types but also to overcome resistance. Targeted radionuclide therapy may synergize well with ICIs since it can promote a pro-inflammatory tumor microenvironment. We investigated the use of a granzyme B targeted peptide (GZP) as a cancer theranostic agent, radiolabeled with (68)Ga ((68)Ga-GZP) as a PET imaging agent and radiolabeled with (90)Y ((90)Y-GZP) as a targeted radionuclide therapy agent for combinational therapy with ICI in murine models of colon cancer. Our results demonstrate that GZP increasingly accumulates in tumor tissue after ICI and that the combination of ICI with (90)Y-GZP promotes a dose-dependent response, achieving curative response in some settings and increased overall survival.