US2021171611A1PendingUtilityA1
Antibody that binds to envelope glycoprotein of sever fever with thrombocytopenia syndrome virus and use for same
Assignee: SEOUL NAT UNIV R&DB FOUNDATIONPriority: Mar 23, 2016Filed: Feb 9, 2021Published: Jun 10, 2021
Est. expiryMar 23, 2036(~9.6 yrs left)· nominal 20-yr term from priority
Inventors:Junho ChungKi Hyun KimHyori KimMyoung-Don OhWan Beom ParkSeungtaek KimJinhee KimJi Young MinMeehyun Ko
C07K 16/104A61P 31/14A61K 39/395C12N 2760/12211G01N 35/0098G01N 33/56983G01N 33/54326C07K 14/005C07K 16/10A61K 39/42C07K 2317/76C12N 15/62C07K 2317/622C07K 14/175G01N 35/00029C07K 2317/565
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Claims
Abstract
The present invention relates to an antibody which specifically binds to the envelope glycoprotein of severe fever with thrombocytopenia syndrome virus (SFTSV), the pathogen of severe fever with thrombocytopenia syndrome (SFTS), and is used in order to effectively detect or diagnosis SFTSV and treat SFTS.
Claims
exact text as granted — not AI-modified1 .- 19 . (canceled)
20 . An antibody which specifically binds to Gc that is an envelope glycoprotein of severe fever with thrombocytopenia syndrome virus, wherein the antibody comprises
a) a light chain complementarity determining region 1 (LCDR1) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 21, 22, 23, 24 and 25, b) a light chain complementarity determining region 2 (LCDR2) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 41, 42, 43, 44 and 45, c) a light chain complementarity determining region 3 (LCDR3) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 61, 62, 63, 64 and 65, d) a heavy chain complementarity determining region 1 (HCDR1) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 26, 27, 28, 29 and 30, e) a heavy chain complementarity determining region 2 (HCDR2) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 46, 47, 48, 49 and 50, and f) a heavy chain complementarity determining region 3 (HCDR3) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 66, 67, 68, 69 and 70.
21 . The antibody according to claim 20 , wherein the antibody comprises
a light chain comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 1, 2, 3, 4 and 5, and a heavy chain comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 6, 7, 8, 9 and 10.
22 . The antibody according to claim 20 , wherein the antibody comprises
a light chain comprising a sequence having 95% or more of sequence identity to any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 1, 2, 3, 4 and 5, and a heavy chain comprising a sequence having 95% or more of sequence identity to any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 6, 7, 8, 9 and 10.
23 . An antibody which specifically binds to Gn that is an envelope glycoprotein of severe fever with thrombocytopenia syndrome virus, wherein the antibody comprises
a) a light chain complementarity determining region 1 (LCDR1) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 101, 102, 103, 104 and 105, b) a light chain complementarity determining region 2 (LCDR2) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 121, 122, 123, 124 and 125, c) a light chain complementarity determining region 3 (LCDR3) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 141, 142, 143, 144 and 145, d) a heavy chain complementarity determining region 1 (HCDR1) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 106, 107, 108, 109 and 110, e) a heavy chain complementarity determining region 2 (HCDR2) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 126, 127, 128, 129 and 130, and f) a heavy chain complementarity determining region 3 (HCDR3) comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 146, 147, 148, 149 and 150.
24 . The antibody according to claim 23 , wherein the antibody comprises
a light chain comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 81, 82, 83, 84 and 85, and a heavy chain comprising any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 86, 87, 88, 89 and 90.
25 . The antibody according to claim 23 , wherein the antibody comprises
a light chain comprising a sequence having 95% or more of sequence identity to any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 81, 82, 83, 84 and 85, and a heavy chain comprising a sequence having 95% or more of sequence identity to any one of amino acids sequence selected from the group consisting of SEQ ID NOs: 86, 87, 88, 89 and 90.
26 . A nucleic acid comprising at least one of
a) a nucleotide sequence encoding a polypeptide comprising a sequence having 95% or more of sequence identity to any one of amino acids selected from the group consisting of SEQ ID NOs: 1, 2, 3, 4 and 5, and a nucleotide sequence encoding a polypeptide comprising a sequence having 95% or more of sequence identity to any one of amino acids selected from the group consisting of SEQ ID NOs: 6, 7, 8, 9 and 10; and b) a nucleotide sequence encoding a polypeptide comprising a sequence having 95% or more of sequence identity to any one of amino acids selected from the group consisting of SEQ ID NOs: 81, 82, 83, 84 and 85, and a nucleotide sequence encoding a polypeptide comprising a sequence having 95% or more of sequence identity to any one of amino acids selected from the group consisting of SEQ ID NOs: 86, 87, 88, 89 and 90.
27 . A vector comprising the nucleic acid of claim 26 .
28 . A host cell comprising the vector of claim 27 .
29 . A composition for diagnosing or detecting SFTSV comprising the antibody of claim 20 .
30 . A kit for diagnosing or detecting SFTSV comprising the antibody of claim 20 .
31 . A method for diagnosing or detecting SFTSV using the antibody of claim 20 .
32 . The method according to claim 31 , wherein the method uses a complex in which the antibody and a magnetic bead are bound.
33 . A pharmaceutical composition comprising the antibody of claim 20 .
34 . A method for preventing or treating SFTS using the antibody of claim claim 20 .Join the waitlist — get patent alerts
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