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Preservation of Quaternary Structure in Thermostable, Lyophilized Filovirus Glycoprotein Vaccines: A Search for Stability-Indicating Assays.
Preston, Kendall B; Monticello, Connor R; Wong, Teri Ann S; To, Albert; Donini, Oreola; Lehrer, Axel T; Randolph, Theodore W.
Affiliation
  • Preston KB; Department of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, CO 80303, USA.
  • Monticello CR; Department of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, CO 80303, USA.
  • Wong TAS; Department of Tropical Medicine, Medical Microbiology & Pharmacology, John A. Burns School of Medicine, University of Hawai'i at Manoa, Honolulu, HI 96813, USA.
  • To A; Department of Tropical Medicine, Medical Microbiology & Pharmacology, John A. Burns School of Medicine, University of Hawai'i at Manoa, Honolulu, HI 96813, USA.
  • Donini O; Soligenix, Inc, Princeton, NJ 08540, USA.
  • Lehrer AT; Department of Tropical Medicine, Medical Microbiology & Pharmacology, John A. Burns School of Medicine, University of Hawai'i at Manoa, Honolulu, HI 96813, USA.
  • Randolph TW; Department of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, CO 80303, USA. Electronic address: theodore.randolph@colorado.edu.
J Pharm Sci ; 109(12): 3716-3727, 2020 12.
Article in En | MEDLINE | ID: mdl-32931778
ABSTRACT
The filoviruses Zaire ebolavirus (EBOV), Marburg marburgvirus (MARV), and Sudan ebolavirus (SUDV) are some of the most lethal infectious agents known. To date, the Zaire ebolavirus vaccine (ERVEBO®) is the only United States Food and Drug Administration (FDA) approved vaccine available for any species of filovirus. However, the ERVEBO® vaccine requires cold-chain storage not to exceed -60 °C. Such cold-chain requirements are difficult to maintain in low- and middle-income countries where filovirus outbreaks originate. To improve the thermostability of filovirus vaccines in order to potentially relax or eliminate these cold-chain requirements, monovalent subunit vaccines consisting of glycoproteins from EBOV, MARV, and SUDV were stabilized within amorphous disaccharide glasses through lyophilization. Lyophilized formulations and liquid controls were incubated for up to 12 weeks at 50 °C to accelerate degradation. To identify a stability-indicating assay appropriate for monitoring protein degradation and immunogenicity loss during these accelerated stability studies, filovirus glycoprotein secondary, tertiary, and quaternary structures and vaccine immunogenicity were measured. Size-exclusion chromatography was the most sensitive indicator of glycoprotein stability in the various formulations for all three filovirus immunogens. Degradation of the test vaccines during accelerated stability studies was reflected in changes in quaternary structure, which were discernible with size-exclusion chromatography. Filovirus glycoproteins in glassy lyophilized formulations retained secondary, tertiary, and quaternary protein structure over the incubation period, whereas the proteins within liquid controls both aggregated to form higher molecular weight species and dissociated from their native quaternary structure to form a variety of structurally-perturbed lower molecular weight species.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vaccines / Glycoproteins / Hemorrhagic Fever, Ebola / Ebolavirus / Marburgvirus Language: En Journal: J Pharm Sci Year: 2020 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vaccines / Glycoproteins / Hemorrhagic Fever, Ebola / Ebolavirus / Marburgvirus Language: En Journal: J Pharm Sci Year: 2020 Type: Article Affiliation country: United States