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Ricin, produced from the castor beans of Ricinus communis, is a cytotoxin that exerts its action by inactivating ribosomes and causing cell death. Accidental (e.g., ingestion of castor beans) and/or intentional (e.g., suicide) exposure to ricin through the oral route is an area of concern from a public health perspective and no current licensed medical interventions exist to protect from the action of the toxin. Therefore, we examined the oral toxicity of ricin in Balb/C mice and developed a robust food deprivation model of ricin oral intoxication that has enabled the assessment of potential antitoxin treatments. A lethal oral dose was identified and mice were found to succumb to the toxin within 48 h of exposure. We then examined whether a despeciated ovine F(ab')2 antibody fragment, that had previously been demonstrated to protect mice from exposure to aerosolised ricin, could also protect against oral intoxication. Mice were challenged orally with an LD99 of ricin, and 89 and 44% of mice exposed to this otherwise lethal exposure survived after receiving either the parent anti-ricin IgG or F(ab')2, respectively. Combined with our previous work, these results further highlight the benefit of ovine-derived polyclonal antibody antitoxin in providing post-exposure protection against ricin intoxication.

Original publication

DOI

10.3390/toxins12120784

Type

Journal article

Journal

Toxins (Basel)

Publication Date

08/12/2020

Volume

12

Keywords

F(ab′)2, IgG, Ricinus communis, antibody, antitoxin, murine, oral, ovine, post-exposure therapy, ricin, Administration, Oral, Animals, Antitoxins, Ricinus communis, Chemical Warfare Agents, Disease Models, Animal, Dose-Response Relationship, Drug, Female, Gastrointestinal Tract, Mice, Mice, Inbred BALB C, Ricin, Sheep, Sheep, Domestic, Treatment Outcome