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Mitigation of total body irradiation-induced mortality and hematopoietic injury of mice by a thrombopoietin mimetic (JNJ-26366821).
Kumar, Vidya P; Holmes-Hampton, Gregory P; Biswas, Shukla; Stone, Sasha; Sharma, Neel Kamal; Hritzo, Bernadette; Guilfoyle, Mary; Eichenbaum, Gary; Guha, Chandan; Ghosh, Sanchita P.
Afiliação
  • Kumar VP; Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, Bethesda, MD, 20889, USA.
  • Holmes-Hampton GP; Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, Bethesda, MD, 20889, USA.
  • Biswas S; Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, Bethesda, MD, 20889, USA.
  • Stone S; Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, Bethesda, MD, 20889, USA.
  • Sharma NK; Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, Bethesda, MD, 20889, USA.
  • Hritzo B; Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, Bethesda, MD, 20889, USA.
  • Guilfoyle M; Office of the Chief Medical Officer, Johnson & Johnson, 410 George Street, New Brunswick, NJ, 08901, USA.
  • Eichenbaum G; Office of the Chief Medical Officer, Johnson & Johnson, 410 George Street, New Brunswick, NJ, 08901, USA.
  • Guha C; Department of Radiation Oncology, Albert Einstein College of Medicine, Bronx, NY, 10467, USA.
  • Ghosh SP; Armed Forces Radiobiology Research Institute, Uniformed Services University of the Health Sciences, Bethesda, MD, 20889, USA. Sanchita.ghosh@usuhs.edu.
Sci Rep ; 12(1): 3485, 2022 03 03.
Article em En | MEDLINE | ID: mdl-35241733
ABSTRACT
The threat of a nuclear attack has increased in recent years highlighting the benefit of developing additional therapies for the treatment of victims suffering from Acute Radiation Syndrome (ARS). In this work, we evaluated the impact of a PEGylated thrombopoietin mimetic peptide, JNJ-26366821, on the mortality and hematopoietic effects associated with ARS in mice exposed to lethal doses of total body irradiation (TBI). JNJ-26366821 was efficacious as a mitigator of mortality and thrombocytopenia associated with ARS in both CD2F1 and C57BL/6 mice exposed to TBI from a cobalt-60 gamma-ray source. Single administration of doses ranging from 0.3 to 1 mg/kg, given 4, 8, 12 or 24 h post-TBI (LD70 dose) increased survival by 30-90% as compared to saline control treatment. At the conclusion of the 30-day study, significant increases in bone marrow colony forming units and megakaryocytes were observed in animals administered JNJ-26366821 compared to those administered saline. In addition, enhanced recovery of FLT3-L levels was observed in JNJ-26366821-treated animals. Probit analysis of survival in the JNJ-26366821- and saline-treated cohorts revealed a dose reduction factor of 1.113 and significant increases in survival for up to 6 months following irradiation. These results support the potential use of JNJ-26366821 as a medical countermeasure for treatment of acute TBI exposure in case of a radiological/nuclear event when administered from 4 to 24 h post-TBI.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trombopoetina / Materiais Biomiméticos / Síndrome Aguda da Radiação / Sistema Hematopoético Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trombopoetina / Materiais Biomiméticos / Síndrome Aguda da Radiação / Sistema Hematopoético Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article