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Radiation Biological Toximetry Using Circulating Cell-Free DNA (cfDNA) for Rapid Radiation/Nuclear Triage.
Okunieff, Paul; Swarts, Steven G; Fenton, Bruce; Zhang, Steven B; Zhang, Zhenhuan; Rice, Lori; Zhou, Daohong; Carrier, France; Zhang, Lurong.
Afiliação
  • Okunieff P; Department of Radiation Oncology, University of Florida, Gainesville, Florida.
  • Swarts SG; Department of Radiation Oncology, University of Florida, Gainesville, Florida.
  • Fenton B; School of Medicine and Dentistry, University of Rochester Medical Center, Rochester, New York.
  • Zhang SB; Department of Radiation Oncology, University of Florida, Gainesville, Florida.
  • Zhang Z; Department of Radiation Oncology, University of Florida, Gainesville, Florida.
  • Rice L; Department of Radiation Oncology, University of Florida, Gainesville, Florida.
  • Zhou D; Department of Biochemistry and Structural Biology, Center for Innovative Drug Discovery (CIDD), University of Texas Health San Antonio, Texas.
  • Carrier F; Department of Radiation Oncology, School of Medicine, University of Maryland, Baltimore, Maryland.
  • Zhang L; Department of Radiation Oncology, University of Florida, Gainesville, Florida.
Radiat Res ; 202(1): 70-79, 2024 07 01.
Article em En | MEDLINE | ID: mdl-38661544
ABSTRACT
Optimal triage biodosimetry would include risk stratification within minutes, and it would provide useful triage despite heterogeneous dosimetry, cytokine therapy, mixed radiation quality, race, and age. For regulatory approval, the U.S. Food and Drug Administration (FDA) Biodosimetry Guidance requires suitability for purpose and a validated species-independent mechanism. Circulating cell-free DNA (cfDNA) concentration assays may provide such triage information. To test this hypothesis, cfDNA concentrations were measured in unprocessed monkey plasma using a branched DNA (bDNA) technique with a laboratory developed test. The cfDNA levels, along with hematopoietic parameters, were measured over a 7-day period in Rhesus macaques receiving total body radiation doses ranging from 1 to 6.5 Gy. Low-dose irradiation (0-2 Gy) was easily distinguished from high-dose whole-body exposures (5.5 and 6.5 Gy). Fold changes in cfDNA in the monkey model were comparable to those measured in a bone marrow transplant patient receiving a supralethal radiation dose, suggesting that the lethal threshold of cfDNA concentrations may be similar across species. Average cfDNA levels were 50 ± 40 ng/mL [±1 standard deviation (SD)] pre-irradiation, 120 ± 13 ng/mL at 1 Gy; 242 ± 71 ng/mL at 2 Gy; 607 ± 54 at 5.5 Gy; and 1585 ± 351 at 6.5 Gy (±1 SD). There was an exponential increase in cfDNA concentration with radiation dose. Comparison of the monkey model with the mouse model and the Guskova model, developed using Chernobyl responder data, further demonstrated correlation across species, supporting a similar mechanism of action. The test is available commercially in a Clinical Laboratory Improvement Amendments (CLIA) ready form in the U.S. and the European Union. The remaining challenges include developing methods for further simplification of specimen processing and assay evaluation, as well as more accurate calibration of the triage category with cfDNA concentration cutoffs.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triagem / Ácidos Nucleicos Livres / Macaca mulatta Limite: Animals / Humans / Male Idioma: En Revista: Radiat Res Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triagem / Ácidos Nucleicos Livres / Macaca mulatta Limite: Animals / Humans / Male Idioma: En Revista: Radiat Res Ano de publicação: 2024 Tipo de documento: Article