Anti-human influenza virus antibody
AssigneeTakara Shuzo Co., Ltd.
InventorsYoshinobu Okuno, Yuji Isegawa, Fuyoko Sasao, Shigeharu Ueda
Life of this patent
Estimating the term…
Loading patent…
AssigneeTakara Shuzo Co., Ltd.
InventorsYoshinobu Okuno, Yuji Isegawa, Fuyoko Sasao, Shigeharu Ueda
Estimating the term…
[Object] To provide an anti-human influenza virus antibody and an immunogenic artificial polypeptide. [Constitution] An anti-human influenza virus antibody which recognizes the stem regions of haemagglutinin molecules of the H1N1 and H2N2 subtypes and has a neutralization activity but does not recognize the stem region of the H3N2 subtype and has no neutralization activity. An immunogenic artificial polypeptide having an antigenicity substantially same as the stem regions of haemagglutinin molecules. An immunogenic artificial polypeptide having an antigenicity substantially same as the stem regions of haemagglutinin molecule and lacking the globular head region of haemagglutinin molecules. [Effect] This antibody is useful in the diagnosis and treatment of influenza A virus, while these polypeptides are useful as a vaccine.
1] an anti-human influenza virus antibody having the following characteristics (a) and (b);
2] An anti-human influenza virus antibody as claimed in claim 1 having the following characteristics (a) and (b):
3] An immunogenic artificial polypeptide having an antigenicity which is substantially same as that of the stem region of haemagglutinin molecule of human influenza A virus.
4] An immunogenic artificial polypeptide as claimed in claim 3, which has an antigenicity which is substantially same as that of the stem region of haemagglutinin molecule of the H1N1 and H2N2 subtypes of human influenza A virus.
5] An immunogenic artificial polypeptide as claimed in claim 4, which contains at least a TGLRN polypeptide sequence represented by the SEQ ID No. 1 in the sequence listing and a GITNKVNSVIEK polypeptide sequence represented by the SEQ ID No. 2 in the sequence listing and has an antigenicity wherein the configuration of these sequences is substantially same as that in the stem region of haemagglutinin molecule of the H1N1 and H2N2 subtypes of human influenza A virus.
6] An immunogenic artificial polypeptide as claimed in claim 3, which has an antigenicity which is substantially same as that of the stem region of haemagglutinin molecule of H3N2 subtype of human influenza A virus.
7] An immunogenic artificial polypeptide as claimed in claim 6, which contains at least a TGMRN polypeptide sequence represented by the SEQ ID No. 3 in the sequence listing and a QINGKLNR(L/V)IEK polypeptide sequence represented by the SEQ ID No. 4 in the sequence listing and has an antigenicity wherein the configuration of these sequences is substantially same as that in the stem region of haemagglutinin molecule of the H3N2 subtype of human influenza A virus.
8] An immunogenic artificial polypeptide having an antigenicity which is substantially same as that of the stem region of haemagglutinin molecule of human influenza A virus and lacking a globular head region of haemagglutinin molecule of human influenza A virus.
9] An immunogenic artificial polypeptide as claimed in claim 8, which has an antigenicity which is substantially same as that of the stem region of haemagglutinin molecule of the H1N1 and H2N2 subtypes of human influenza A virus and lacks a globular head region of haemagglutinin molecule of human influenza A virus.
10] An immunogenic artificial polypeptide as claimed in claim 9, which contains at least a TGLRN polypeptide sequence represented by the SEQ ID No. 1 in the sequence listing and a GITNKVNSVIEK polypeptide sequence represented by the SEQ ID No. 2 in the sequence listing and has an antigenicity wherein the configuration of these sequences is substantially same as that in the stem region of haemagglutinin molecule of the H1N1 and H2N2 subtypes of human influenza A virus, and lacks a globular head region of haemagglutinin molecule of human influenza A virus.
11] An immunogenic artificial polypeptide as claimed in claim 8, which has an antigenicity which is substantially same as that of the stem region of haemagglutinin molecule of H3N2 subtype of human influenza A virus and lacks a globular head region of haemagglutinin molecule of human influenza A virus.
12] An immunogenic artificial polypeptide as claimed in claim 11, which contains at least a TGMRN polypeptide sequence represented by the SEQ ID No. 3 in the sequence listing and a QINGKLNR(L/V)IEK polypeptide sequence represented by the SEQ ID No. 4 in the sequence listing and has an antigenicity wherein the configuration of these sequences is substantially same as that in the stem region of haemagglutinin molecules of the H3N2 subtype of human influenza A virus, and lacks a globular head region of haemagglutinin molecule of human influenza A virus.
13] An immunogenic artificial polypeptide as claimed in claim 8 characterized by being obtained by separating from haemagglutinin molecules of human influenza A virus which have been treated with a protease.
14] An immunogenic artificial polypeptide as claimed in claim 8 characterized by being obtained by separating from haemagglutinin molecules of human influenza A virus which have been treated with a proteinase.
15] An immunogenic artificial polypeptide as claimed in claim 8 characterized by being obtained by separating from haemagglutinin molecules of human influenza A virus which have been treated with a proteinase K.
16] An isolated gene which codes for the polypeptide of claim 3.
17] An isolated gene as claimed in claim 16, wherein said gene has a DNA sequene represented by the SEQ ID No. 46.
18] An isolated gene which codes for the polypeptide of claim 8.
19] An isolated gene as claimed in claim 18, wherein said gene is selected from a gene having a DNA sequene represented by the SEQ ID No. 49 and a gene having a DNA sequence represented by the SEQ ID No. 57.