US2013216563A1PendingUtilityA1
Immunogenic Polypeptides Encoded by MAGE Minigenes and Uses Thereof
Est. expiryMay 10, 2020(expired)· nominal 20-yr term from priority
Inventors:Neil BerinsteinJames TartagliaJohn A. TinePhilippe MoingeonThierry Boon-FalleurPierre Vander Bruggen
A61P 35/00C07K 14/47A61K 2039/53C12N 2799/021C12N 2799/023C12N 15/62A61K 48/00C07K 14/4748A61P 37/04A61K 39/00
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Claims
Abstract
The invention discloses immunogenic polypeptides comprising several MAGE-specific antigen epitopes selected from different (i.e. discrete) members of the MAGE protein family, nucleic acids coding therefor, recombinant viruses and/or cells comprising said nucleic acids, and compositions thereof. Methods for eliciting or inducing MAGE-specific immune responses utilizing the aforementioned immunogenic agents are also disclosed.
Claims
exact text as granted — not AI-modified1 . An immunogenic polypeptide comprising a first MAGE-specific antigen epitope of a member selected from the group consisting of MAGE 1, MAGE 2 and MAGE 3, and a second MAGE-specific antigen epitope of a different member selected from said group.
2 . The polypeptide of claim 1 wherein the first MAGE-specific antigen epitope is from MAGE 1 and the second MAGE-specific antigen epitope is from MAGE 3.
3 . The polypeptide of claim 2 wherein the epitope from MAGE 1 has the sequence EADPTGHSY and the epitope of MAGE 3 has the sequence EVDPIGHLY.
4 . The polypeptide of claim 1 wherein the first MAGE-specific antigen epitope and the second MAGE-specific antigen epitope are adjoined together.
5 . The polypeptide of claim 1 wherein an amino acid linker sequence joins the first and second MAGE-specific antigen epitope.
6 . The polypeptide of claim 5 wherein the amino acid linker sequence further comprises a protease cleavage site.
7 . The polypeptide of claim 1 comprising the amino acid sequence of SEQ. ID NO: 1.
8 . The polypeptide of claim 1 having the amino acid sequence of SEQ. ID NO.: 1.
9 . A pharmaceutical composition comprising the polypeptide of claim 1 , and a pharmaceutically acceptable diluent or carrier.
10 . The composition of claim 9 further comprising an adjuvant.
11 . A nucleic acid encodes the polypeptide of claim 1 .
12 . (canceled)
13 . The nucleic acid of claim 11 having the sequence of SEQ. ID NO: 2.
14 . The nucleic acid of any one of claims 11 through 13 wherein the nucleic acid is selected from the group consisting of viral nucleic acid, plasmid, bacterial DNA, naked/free DNA, and RNA.
15 - 18 . (canceled)
19 . A pharmaceutical composition comprising the nucleic acid of claim 11 and a pharmaceutically acceptable diluent or carrier.
20 - 32 . (canceled)
33 . A method of inducing an immune response in an animal directed against a member selected from the group consisting of:
a polypeptide as claimed in any one of claim 1 through 8 ; a MAGE-specific antigen epitope of said polypeptide; a MAGE protein or fragment thereof comprising a MAGE-specific antigen epitope of said polypeptide; cells expressing said MAGE protein or fragment thereof, polypeptide, MAGE-specific antigen epitope of the polypeptide; and, cells binding said MAGE protein or fragment thereof, polypeptide, MAGE-specific antigen epitope of the polypeptide; comprising administering to said animal a recombinant virus according to any one of claims 27 through 30 in an amount sufficient to induce an immune response.
34 - 40 . (canceled)
41 . A method for preparing a polypeptide of claim 1 comprising expressing a nucleic acid encoding the polypeptide in a host cell and isolating the polypeptide.
42 . The method of claim 41 wherein the polypeptide is expressed using a vector selected from the group consisting of viral nucleic acid, plasmid, bacterial DNA, naked/free DNA, and RNA.Cited by (0)
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