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US 12,673,095 B2Granted
Polynucleotides encoding SARS-COV-2 antigens and use thereof in the medical field as vaccines
AssigneeTakis S.R.L.
InventorsLuigi Aurisicchio, Emanuele Marra, Giuseppe Roscilli, Fabio Palombo, Mariano Maffei, Alessia Muzi
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Abstract
The present invention relates to polynucleotides encoding antigens of the SARS-CoV-2 coronavirus spike protein and use thereof in the medical field as vaccines for the prevention and treatment of COVID-19 infection.
Claims12
A polynucleotide encoding an amino acid sequence, an expression vector comprising said polynucleotide, or a pharmaceutical composition comprising said polynucleotide or expression vector in combination with one or more excipients and/or adjuvants, wherein the polynucleotide comprises or consists of a sequence selected from:
- SEQ ID NO:1 fused to the C-terminal of the tissue plasminogen activator (TPA) secretion leader sequence, said sequence SEQ ID NO:1 encoding an amino acid sequence consisting of the receptor binding domain (RBD) domain of the S1 subunit of the spike protein of the SARS-CoV-2 virus or of variants thereof;
- a sequence having a percent identity greater than or equal to 80% compared to sequence SEQ ID NO:1, selected from SEQ ID NO:14, SEQ ID NO:15, and SEQ ID NO:21, alone or fused to the C-terminal of the tissue plasminogen activator (TPA) secretion leader sequence;
- SEQ ID NO:2, which encodes an amino acid sequence consisting of the N-terminal domain (NTD) and RBD domains of the S1 subunit of the spike protein of the SARS-CoV-2 virus;
- SEQ ID NO:3, which encodes an amino acid sequence consisting of the NTD, RBD, C-terminal domain 2 (CTD2) and C-terminal domain 3 (CTD3) domains of the S1 subunit of the spike protein of the SARS-CoV-2 virus;
- SEQ ID NO:5, which encodes an amino acid sequence consisting of the spike protein of the SARS-CoV-2 virus;
- and
- SEQ ID NO:4, which encodes an amino acid sequence consisting of the RBD domain of the S1 subunit of the spike protein of the SARS-CoV-2 virus, said domain being fused at the N-terminal end to the IgK leader sequence and at the C-terminal end to the Fc immunomodulating sequence.
4 more elements
Dependencies are inferred from the claim text.