Characterization of pritumumab in murine models and primate safety study

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 <sup>89</sup>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.

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Publication Details

Journal
Scientific Reports
Published
2025-03-25
DOI
https://doi.org/10.1038/s41598-025-95360-9
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
0.00

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Characterization of pritumumab in murine models and primate safety study

Kishore Gangangari, Nagavarakishore Pillarsetty, Pengfei Jiang, Sneha L. Kesari et al.
Scientific Reports
Cancer Immunotherapy and Biomarkers
article

Characterization of pritumumab in murine models and primate safety study

Kishore Gangangari, Nagavarakishore Pillarsetty, Pengfei Jiang, Sneha L. Kesari, Rajesh Mukthavaram, Santosh Kesari, Vijay Padul, P. Kesari, Elnaz Rahbarlayegh, Mark C. Glassy, Avani A. Mody
article en

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 <sup>89</sup>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.

Scientific ReportsVol. 15(1)
Memorial Sloan Kettering Cancer Center (US), Neurosciences Institute (US), University of California San Diego (US), Saint John's Health Center (US)
Memorial Sloan-Kettering Cancer Center
Openalex Percentile: Top 92%
Cancer Immunotherapy and Biomarkers
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Characterization of pritumumab in murine models and primate safety study — Kishore Gangangari, Nagavarakishore Pillarsetty, et al. · Scientific Reports (2025) | TGRS Research Map | TGRS