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DNA origami presenting the receptor binding domain of SARS-CoV-2 elicit robust protective immune response.
Oktay, Esra; Alem, Farhang; Hernandez, Keziah; Girgis, Michael; Green, Christopher; Mathur, Divita; Medintz, Igor L; Narayanan, Aarthi; Veneziano, Remi.
  • Oktay E; Department of Bioengineering, George Mason University, Fairfax, VA, 22030, USA.
  • Alem F; National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, VA, 20110, USA.
  • Hernandez K; National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, VA, 20110, USA.
  • Girgis M; Department of Bioengineering, George Mason University, Fairfax, VA, 22030, USA.
  • Green C; Center for Bio/Molecular Science and Engineering Code 6900, U.S. Naval Research Laboratory, Washington, DC, USA.
  • Mathur D; Department of Chemistry, Case Western Reserve University, Cleveland, OH, USA.
  • Medintz IL; Center for Bio/Molecular Science and Engineering Code 6900, U.S. Naval Research Laboratory, Washington, DC, USA.
  • Narayanan A; National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, VA, 20110, USA. anaraya1@gmu.edu.
  • Veneziano R; Department of Bioengineering, George Mason University, Fairfax, VA, 22030, USA. rvenezia@gmu.edu.
Commun Biol ; 6(1): 308, 2023 03 23.
Article in English | MEDLINE | ID: covidwho-2274811
ABSTRACT
Effective and safe vaccines are invaluable tools in the arsenal to fight infectious diseases. The rapid spreading of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) responsible for the coronavirus disease 2019 pandemic has highlighted the need to develop methods for rapid and efficient vaccine development. DNA origami nanoparticles (DNA-NPs) presenting multiple antigens in prescribed nanoscale patterns have recently emerged as a safe, efficient, and easily scalable alternative for rational design of vaccines. Here, we are leveraging the unique properties of these DNA-NPs and demonstrate that precisely patterning ten copies of a reconstituted trimer of the receptor binding domain (RBD) of SARS-CoV-2 along with CpG adjuvants on the DNA-NPs is able to elicit a robust protective immunity against SARS-CoV-2 in a mouse model. Our results demonstrate the potential of our DNA-NP-based approach for developing safe and effective nanovaccines against infectious diseases with prolonged antibody response and effective protection in the context of a viral challenge.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Vaccines / COVID-19 Topics: Vaccines Limits: Animals Language: English Journal: Commun Biol Year: 2023 Document Type: Article Affiliation country: S42003-023-04689-2

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Vaccines / COVID-19 Topics: Vaccines Limits: Animals Language: English Journal: Commun Biol Year: 2023 Document Type: Article Affiliation country: S42003-023-04689-2