US2006074038A1PendingUtilityA1
Her-2 neu dna vaccine having anti-cancer activity
Est. expiryJul 16, 2022(expired)· nominal 20-yr term from priority
C12N 2840/203A61K 2039/53C07K 2319/02A61K 2039/55522A61K 39/001106C12N 15/85A61P 35/00
49
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Claims
Abstract
The present invention relates to human Her-2/neu expressing plasmid constructs having anti-cancer activity and a DNA vaccine comprising same for preventing and/or treating cancer. The Her-2/neu DNA vaccines of the present invention can be effectively used as a therapeutic vaccine in reducing metastasis after tumor surgery or as a prophylactic vaccine for people with genetic high risk.
Claims
exact text as granted — not AI-modified1 . An Her-2/neu plasmid construct having anti-cancer activity which is prepared by inserting a truncated human Her-2/neu gene lacking the intracellular domain into plasmid pTV2 or pCK.
2 . The plasmid construct of claim 1 , wherein the human Her-2/neu gene has the nucleotide sequence of SEQ ID NO: 2.
3 . The plasmid construct of claim 2 , which is pNeu TM (KCCM-10393) or pCK TM (KCCM-10396)
4 . The plasmid construct of claim 1 , wherein the truncated human Her-2/neu gene further lacks the transmembrane domain.
5 . The plasmid construct of claim 4 , wherein the human Her-2/neu gene has the nucleotide of SEQ ID NO: 3.
6 . The plasmid construct of claim 5 , which is pNeu ECD (KCCM-10394) or pCK ECD (KCCM-10395).
7 . The plasmid construct of claim 1 , wherein the signal peptide of the human Her-2/neu gene is replaced by the signal peptide of herpes simplex type I glycoprotein D (gD).
8 . The plasmid construct of claim 7 , which is pNeu TM-gDs .
9 . The plasmid construct of claim 4 , wherein the signal peptide of the human Her-2/neu gene is replaced by the signal peptide of herpes simplex type I glycoprotein D (gD).
10 . The plasmid construct of claim 7 , which is pNeu ECD-gDs .
11 . The plasmid construct of claim 1 , which further translates a cytokine gene besides the human Her-2/neu gene.
12 . The plasmid construct of claim 11 , wherein the cytokine gene is selected from the group consisting of granulocyte-macrophage colony-stimulating factor (GM-CSF), FMS-like tyrosine kinase 3 ligand (Flt3L), early T lymphocyte activation-1 (Eta-1), interleukin-12 (IL-12), IL-15 and IL-18.
13 . A DNA vaccine for preventing and/or treating cancer, which comprises the plasmid construct of claim 1 as an effective ingredient and a pharmaceutically acceptable carrier.
14 . The DNA vaccine of claim 13 , which further comprises a cytokine gene expressing plasmid.
15 . The DNA vaccine of claim 14 , wherein the cytokine gene is selected from the group consisting of GM-CSF, Flt3L, Eta-1, IL-12, IL-15 and IL-18.
16 . A method for preventing and/or treating cancer, which comprises the step of administering an effective amount of the DNA vaccine of claim 13.Join the waitlist — get patent alerts
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