US2018371411A1PendingUtilityA1
Kidney-specific tumor vaccine directed against kidney tumor antigen g-250
Est. expiryFeb 14, 2020(expired)· nominal 20-yr term from priority
A61K 2039/868A61P 35/04A61K 38/00A61K 2039/55516A61K 2039/55522C07K 14/535A61P 35/00A61K 2039/54A61K 2039/6031C07K 14/4748A61K 9/0019C12N 2501/22A61K 2039/53C07K 14/47C12N 15/85A61K 39/0011A61K 2039/5154A61K 2039/5158C12N 5/0636A61K 40/42A61K 40/24A61K 40/19A61K 40/11A61K 2239/56
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Claims
Abstract
This invention provides an anti-cancer immunogenic agent(s) (e.g. vaccines) that elicit an immune response specifically directed against renal cell cancers expressing a G250 antigenic marker. Preferred immunogenic agents comprise a chimeric molecule comprising a kidney cancer specific antigen (G250) attached to a granulocyte-macrophage colony stimulating factor (GM-CSF). The agents are useful in a wide variety of treatment modalities including, but not limited to protein vaccination, DNA vaccination, and adoptive immunotherapy.
Claims
exact text as granted — not AI-modified1 - 85 . (canceled)
86 . A vector gene delivery system, comprising a vector that comprises a nucleic acid encoding a fusion protein comprising a human G250 kidney cancer specific antigen attached to a human granulocyte macrophage colony stimulating factor (GM-CSF), wherein the G250 antigen is encoded by the nucleotide sequence of SEQ ID NO:23 and the GM-CSF is encoded by the nucleotide sequence of SEQ ID NO:24.
87 . The vector gene delivery system of claim 86 , wherein the G250 antigen and the GM-CSF are joined by a peptide linker ranging in length from 2 to about 20 amino acids.
88 . The vector gene delivery system of claim 87 , wherein the peptide linker is -Arg-Arg-.
89 . The vector gene delivery system of claim 86 , wherein the fusion protein comprises the amino acid sequence of SEQ ID NO:1.
90 . The vector gene delivery system of claim 86 , wherein the nucleic acid is operably linked to one or more regulatory elements for gene expression.
91 . The vector gene delivery system of claim 90 , wherein the nucleic acid is operably linked to a promoter.
92 . The vector gene delivery system of claim 86 , wherein the vector is a viral vector.
93 . The vector gene delivery system of claim 92 , wherein the viral vector is an adeno-associated virus (AAV), adenoviral, retroviral, lentiviral, simian virus 40, or baculoviral vector.
94 . A method of inducing an immune response against a G250 antigen in a subject, the method comprising administering to the subject the vector gene delivery system of claim 86 .
95 . The method of claim 94 , wherein the subject is a human.
96 . A method of activating an immune cell, the method comprising transfecting or transducing the immune cell in vitro or ex vivo with the vector gene delivery system of claim 86 .
97 . The method of claim 96 , wherein the immune cell is a dendritic cell, an antigen presenting cell, a B-cell, a T-cell, a monocyte, a peripheral blood lymphocyte, or a tumor infiltrating lymphocyte.
98 . The method of claim 96 , further comprising expanding the activated immune cell in culture.
99 . The method of claim 96 , wherein the immune cell is from a human subject.
100 . The method of claim 96 , further comprising administering the activated immune cell to a subject.
101 . The method of claim 100 , wherein the immune cell is autologous to the subject.
102 . The method of claim 100 , wherein the subject is a human.
103 . An immune cell comprising the vector gene delivery system of claim 86 .
104 . A dendritic cell comprising the vector gene delivery system of claim 86 .Cited by (0)
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