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Development of a biodosimeter for radiation triage using novel blood protein biomarker panels in humans and non-human primates. International journal of radiation biology Balog, R. P., Bacher, R., Chang, P., Greenstein, M., Jammalamadaka, S., Javitz, H., Knox, S. J., Lee, S., Lin, H., Shaler, T., Shura, L., Stein, P., Todd, K., Cooper, D. E. 2019: 1–13

Abstract

PURPOSE: In a significant nuclear event, hundreds of thousands of individuals will require rapid triage for absorbed radiation to ensure effective medical treatment and efficient use of medical resources. We are developing a rapid screening method to assess whether an individual received an absorbed dose of =2Gy based on the analysis of a specific panel of blood proteins in a fingerstick blood sample.MATERIALS AND METHODS: We studied a data set of 1051 human blood samples obtained from radiotherapy patients, normal healthy individuals, and several special population groups. We compared the findings in humans with those from irradiation studies in non-human primates (NHPs).RESULTS: We identified a panel of three protein biomarkers, salivary alpha amylase (AMY1), Flt3 ligand (FLT3L), and monocyte chemotactic protein 1 (MCP1), which are upregulated in human patients receiving fractionated doses of total body irradiation (TBI) therapy as a treatment for cancer. These proteins exhibited a similar radiation response in NHPs after single acute or fractionated doses of ionizing radiation.CONCLUSION: Our work provides confidence in this biomarker panel for biodosimetry triage using fingerstick blood samples and in the use of NHPs as a model for irradiated humans.

View details for PubMedID 30605362