Abstract

Bone marrow failure and hematopoietic damage is one of the major consequences of irradiation-induced lethality. There is an immediate need to develop medical countermeasures (MCMs) to combat irradiation-induced lethality. We tested the efficacy of CDX-301, developed by Celldex Therapeutics Inc., in mice exposed to Co-60 gamma total body irradiation (TBI). The drug demonstrated its efficacy both as a prophylactic countermeasure and a mitigator in CD2F1 mice exposed to TBI. A single dose of CDX-301 administered 24 h prior to 24 h post–exposure conferred significant survival. Accelerated recovery from irradiation-induced peripheral blood cytopenia, bone marrow damage as well as apoptosis in sternum was observed in mice pre-treated with CDX-301. Analysis of splenocytes revealed alterations in T cell profiles that were dependent on the time of drug administration. Prophylactic treatment of CDX-301 resulted in increased splenic CD3+ T cells, specifically CD4+T helper cells, compared to splenocytes from non-irradiated mice. These results indicate that CDX-301 is a promising radiation countermeasure and demonstrate its capability to protect cells within hematopoietic organs. These data support potential use of CDX-301, both pre- and post-radiation, against hematopoietic acute radiation syndrome with a broad window for medical management in a radiological or nuclear event.

Details

Title
CDX-301: a novel medical countermeasure for hematopoietic acute radiation syndrome in mice
Author
Satyamitra Merriline 1 ; Cary, Lynnette 2 ; Dunn, Dylan 2 ; Holmes-Hampton, Gregory P 2 ; Thomas, Lawrence J 3 ; Ghosh, Sanchita P 2 

 Radiation and Nuclear Countermeasure Program, DAIT, NIAID, Rockville, USA (GRID:grid.419681.3) (ISNI:0000 0001 2164 9667) 
 Uniformed Services University of the Health Sciences Bethesda, Armed Forces Radiobiology Research Institute, Bethesda, USA (GRID:grid.265436.0) (ISNI:0000 0001 0421 5525) 
 Celldex Therapeutics, Inc., Needham, USA (GRID:grid.417695.8) 
Publication year
2020
Publication date
2020
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2350893758
Copyright
This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.