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公开(公告)号:US20230381296A1
公开(公告)日:2023-11-30
申请号:US18031570
申请日:2021-10-13
Inventor: Shinya OKAMURA , Akiho KASHIWABARA , Hirotaka EBINA
IPC: A61K39/215 , C12N7/00 , C12N9/10 , C12N9/16 , A61P31/14
CPC classification number: A61K39/215 , C12N7/00 , C12N9/1007 , C12Y201/01056 , C12Y201/01057 , C12N9/16 , C12Y301/03084 , A61P31/14 , C12N2770/20022 , C12N2770/20034 , C12N2770/20071 , A61K2039/5254
Abstract: Provided is a strain that is effective as an active ingredient of a vaccine against betacoronavirus. This SARS-CoV-2 includes non-structural protein(s) that has the following responsible mutation(s): a mutation in the amino acid residue corresponding to the L of position 445 of SEQ ID NO: 1 in NSP3; a mutation in the amino acid residues corresponding to the G of position 248 and the G of position 416 of SEQ ID NO: 2 in NSP14; and/or a mutation in the amino acid residue corresponding to the V of position 67 of SEQ ID NO: 3 in NSP16.
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公开(公告)号:US20250002871A1
公开(公告)日:2025-01-02
申请号:US18708189
申请日:2022-11-07
Inventor: Shiro TAKEKAWA , Hirotaka EBINA , Shinya OKAMURA , Akiho YOSHIDA
Abstract: The purpose of the present invention is to provide a strain that is useful as a novel betacoronavirus vaccine. It is revealed that novel betacoronavirus, according to the present invention, having a prescribed substitution mutation relating to temperature sensitivity in combination with a prescribed deletion mutation relating to attenuation, is useful as a betacoronavirus vaccine strain having excellent attenuated characteristics.
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公开(公告)号:US20230374469A1
公开(公告)日:2023-11-23
申请号:US18031599
申请日:2021-10-13
Inventor: Shinya OKAMURA , Akiho KASHIWABARA , Hirotaka EBINA
IPC: C12N7/00 , C07K14/165 , A61P31/14
CPC classification number: C12N7/00 , C07K14/165 , A61P31/14 , A61K2039/5254
Abstract: Strains that is effective as the active component of a vaccine against the betacoronavirus is provided. A SARS-CoV-2 containing structural protein(s) and/or non-structural protein(s) having the following mutation(s): the amino acid residue mutations in NSP3, corresponding to V at position 404, L at position 445, K at position 1792 and/or D at position 1832 in SEQ ID No. 1; the amino acid residue mutations in NSP14, corresponding to G at position 248, G at position 416, and/or A at position 504 in SEQ ID No. 2; the amino acid residue mutation in NSP16, corresponding to V at position 67 in SEQ ID No. 3; the amino acid residue mutations in the spike, corresponding to L at position 54, T at position 739 and/or A at position 879 in SEQ ID No. 4; the amino acid residue mutation in the envelope, corresponding to L at position 28 in SEQ ID No. 5; and/or, the amino acid residue mutation in the nucleocapsid, corresponding to S at position 2 in SEQ ID No. 6;
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