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Development of an IgG-Fc fusion COVID-19 subunit vaccine, AKS-452.
Alleva, David G; Delpero, Andrea R; Scully, Melanie M; Murikipudi, Sylaja; Ragupathy, Ramya; Greaves, Emma K; Sathiyaseelan, Thillainaygam; Haworth, Jeffrey R; Shah, Nishit J; Rao, Vidhya; Nagre, Shashikant; Lancaster, Thomas M; Webb, Sarah S; Jasa, Allison I; Ronca, Shannon E; Green, Freedom M; Elyard, Hanne Andersen; Yee, JoAnn; Klein, Jeffrey; Karnes, Larry; Sollie, Frans; Zion, Todd C.
Afiliación
  • Alleva DG; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Delpero AR; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Scully MM; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Murikipudi S; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Ragupathy R; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Greaves EK; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Sathiyaseelan T; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Haworth JR; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Shah NJ; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Rao V; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Nagre S; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Lancaster TM; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States.
  • Webb SS; Biomere Biomedical Research Models, 57 Union St., Worcester, MA 01608, United States.
  • Jasa AI; Biomere Biomedical Research Models, 57 Union St., Worcester, MA 01608, United States.
  • Ronca SE; Feigin ABSL-3 Facility, Baylor, College of Medicine, 1102 Bates Ave, 300.15, Houston, TX 77030, United States.
  • Green FM; Feigin ABSL-3 Facility, Baylor, College of Medicine, 1102 Bates Ave, 300.15, Houston, TX 77030, United States.
  • Elyard HA; BIOQUAL, Inc., 9600 Medical Center Drive, Suite 101, Rockville, MD 20850-3336, United States.
  • Yee J; Primate Assay Laboratory, CA National Primate Research Center, University of California, Davis, CA 95616, United States.
  • Klein J; Sinclair Research Center, 562 State Road DD, Auxvasse, MO 65231, United States.
  • Karnes L; Sinclair Research Center, 562 State Road DD, Auxvasse, MO 65231, United States.
  • Sollie F; Pharmaceutical Research Associates Group B.V., Amerikaweg 18, 9407 TK Assen, Netherlands.
  • Zion TC; Akston Biosciences Corporation., 100 Cummings Center, Suite 454C, Beverly, MA 01915, United States. Electronic address: todd.zion@akstonbio.com.
Vaccine ; 39(45): 6601-6613, 2021 10 29.
Article en En | MEDLINE | ID: mdl-34642088
AKS-452 is a biologically-engineered vaccine comprising an Fc fusion protein of the SARS-CoV-2 viral spike protein receptor binding domain antigen (Ag) and human IgG1 Fc (SP/RBD-Fc) in clinical development for the induction and augmentation of neutralizing IgG titers against SARS-CoV-2 viral infection to address the COVID-19 pandemic. The Fc moiety is designed to enhance immunogenicity by increasing uptake via Fc-receptors (FcγR) on Ag-presenting cells (APCs) and prolonging exposure due to neonatal Fc receptor (FcRn) recycling. AKS-452 induced approximately 20-fold greater neutralizing IgG titers in mice relative to those induced by SP/RBD without the Fc moiety and induced comparable long-term neutralizing titers with a single dose vs. two doses. To further enhance immunogenicity, AKS-452 was evaluated in formulations containing a panel of adjuvants in which the water-in-oil adjuvant, Montanide™ ISA 720, enhanced neutralizing IgG titers by approximately 7-fold after one and two doses in mice, including the neutralization of live SARS-CoV-2 virus infection of VERO-E6 cells. Furthermore, ISA 720-adjuvanted AKS-452 was immunogenic in rabbits and non-human primates (NHPs) and protected from infection and clinical symptoms with live SARS-CoV-2 virus in NHPs (USA-WA1/2020 viral strain) and the K18 human ACE2-trangenic (K18-huACE2-Tg) mouse (South African B.1.351 viral variant). These preclinical studies support the initiation of Phase I clinical studies with adjuvanted AKS-452 with the expectation that this room-temperature stable, Fc-fusion subunit vaccine can be rapidly and inexpensively manufactured to provide billions of doses per year especially in regions where the cold-chain is difficult to maintain.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Glicoproteína de la Espiga del Coronavirus / Vacunas contra la COVID-19 / COVID-19 Límite: Animals Idioma: En Revista: Vaccine Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Glicoproteína de la Espiga del Coronavirus / Vacunas contra la COVID-19 / COVID-19 Límite: Animals Idioma: En Revista: Vaccine Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos