Characterization of pritumumab in murine models and primate safety study.
1/5 보강
Pritumumab is a human IgG1 kappa antibody that targets ecto-domain vimentin (EDV) which is overexpressed in several malignant tumors including glioblastomas.
APA
Mody AA, Mukthavaram R, et al. (2025). Characterization of pritumumab in murine models and primate safety study.. Scientific reports, 15(1), 10178. https://doi.org/10.1038/s41598-025-95360-9
MLA
Mody AA, et al.. "Characterization of pritumumab in murine models and primate safety study.." Scientific reports, vol. 15, no. 1, 2025, pp. 10178.
PMID
40128557
Abstract
Pritumumab is a human IgG1 kappa antibody that targets ecto-domain vimentin (EDV) which is overexpressed in several malignant tumors including glioblastomas. To understand preclinical biological activity and safety of pritumumab derived from Chinese hamster ovary (CHO) cells, we evaluated tumor targeting ability, brain-tumor barrier permeability, growth inhibition, and primate safety studies. In-vivo and ex-vivo imaging studies demonstrate pritumumab to cross the blood brain/blood tumor barrier and an Zr-labeled pritumumab immunoconjugate showed the antibody specifically targeted tumor cells. In mouse xenograft models, pritumumab inhibited the growth of U251 glioblastoma and PANC-1 pancreatic cancer cells. A 29-day intravenous toxicology study in cynomolgus monkeys was carried out to analyze the safety and toxicity of pritumumab, and no toxic effects were observed. Overall, these data together suggest pritumumab is biologically active and animal models can be used to further understand the various functions of the antibody. Clinical trials in brain cancer patients assessing safety and efficacy of pritumumab as a therapeutic for brain cancer are in process.
MeSH Terms
Animals; Mice; Humans; Macaca fascicularis; Antibodies, Monoclonal; CHO Cells; Cell Line, Tumor; Xenograft Model Antitumor Assays; Cricetulus; Female; Blood-Brain Barrier; Brain Neoplasms; Vimentin; Antibodies, Monoclonal, Humanized; Glioblastoma; Pancreatic Neoplasms; Cricetinae; Disease Models, Animal