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Toxicity and Immunogenicity of a Tardigrade Cytosolic Abundant Heat Soluble Protein in Mice.
Esterly, Harrison J; Crilly, Candice J; Piszkiewicz, Samantha; Shovlin, Dane J; Pielak, Gary J; Christian, Brooke E.
Affiliation
  • Esterly HJ; Department of Chemistry and Fermentation Sciences, Appalachian State University, Boone, NC, United States.
  • Crilly CJ; Department of Chemistry, University of North Carolina, Chapel Hill, NC, United States.
  • Piszkiewicz S; Department of Chemistry, University of North Carolina, Chapel Hill, NC, United States.
  • Shovlin DJ; Department of Chemistry, University of North Carolina, Chapel Hill, NC, United States.
  • Pielak GJ; Department of Chemistry and Fermentation Sciences, Appalachian State University, Boone, NC, United States.
  • Christian BE; Department of Chemistry, University of North Carolina, Chapel Hill, NC, United States.
Front Pharmacol ; 11: 565969, 2020.
Article in En | MEDLINE | ID: mdl-33117164
ABSTRACT
Tardigrades are microscopic animals well-known for their stress tolerance, including the ability to survive desiccation. This survival requires cytosolic abundant heat soluble (CAHS) proteins. CAHS D protects enzymes from desiccation- and lyophilization-induced inactivation in vitro and has the potential to stabilize protein-based therapeutics, including vaccines. Here, we investigate whether purified recombinant CAHS D causes hemolysis or a toxic or immunogenic response following intraperitoneal injection in mice. CAHS D did not cause hemolysis, and all mice survived the 28-day monitoring period. The mice gained weight normally and developed anti-CAHS D antibodies but did not show upregulation of the inflammatory cytokines interleukin-6 and tumor necrosis factor alpha. In summary, CAHS D is not toxic and does not promote an inflammatory immune response in mice under the conditions used here, suggesting the reasonability of further study for use as stabilizers of protein-based therapeutics.
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Full text: 1 Database: MEDLINE Language: En Journal: Front Pharmacol Year: 2020 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Language: En Journal: Front Pharmacol Year: 2020 Type: Article Affiliation country: United States