Parovirus having a CpG-enriched genome useful for cancer therapy

US10098917B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10098917-B2
Application numberUS-201313887029-A
CountryUS
Kind codeB2
Filing dateMay 3, 2013
Priority dateDec 28, 2007
Publication dateOct 16, 2018
Grant dateOct 16, 2018

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

A parvovirus characterized by a CpG-enriched genome, wherein the genome contains at least 2 additional CpG inserts that are not present in the wild type genome is described as well as the use of said parvovirus, e.g., a parvovirus based on parvovirus H1, LuIII, Mouse minute virus (MMV), Mouse parvovirus (MPV), Rat minute virus (RMV), Rat parvovirus (RPV), Rat virus (RV), vectors based on the foregoing viral species, and/or cells capable of actively producing the foregoing viral species for the preparation of a pharmaceutical composition, e.g., for the treatment of cancer, preferably pancreas carcinoma, hepatoma or lymphoma.

First claim

Opening claim text (preview).

The invention claimed is: 1. A replication-competent parvovirus comprising a CpG motif-enriched genome, wherein the parvovirus genome contains three AACGTT motifs and three GTCGTT motifs within the untranslated region at the 3′ end of the VP transcription unit that are not present in the wild type genome, and wherein said parvovirus is parvovirus H1 (H-1 PV) and wherein the virus is stable through multiple passages. 2. A pharmaceutical composition containing the replication-competent parvovirus of claim 1 . 3. A method of stimulating an immune response to treat a tumor in a patient in need thereof, said method comprising, (a) infecting autologous tumor cells with an effective amount of a replication-competent parvovirus comprising a CpG motif-enriched genome, wherein the genome contains the nucleotide sequence as set forth in SEQ ID NO: 1 within the untranslated region at the 3′ end of the VP transcription unit, wherein said autologous tumor cells is pancreatic tumor cells or hepatoma cells; (b) irradiating said infected autologous tumor cells; (b) preparing a vaccine composition comprising the irradiated infected autologous tumor cells; and (c) subcutaneously administering to the patient in need thereof an effective amount of said vaccine comprising the irradiated infected autologous tumor cells that enhance innate and adaptive immune response, thereby treating tumor in said patient.

Assignees

Inventors

Classifications

  • specific for leukemia · CPC title

  • Antineoplastic agents · CPC title

  • Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof (preparing medicinal viral antigen or antibody compositions, e.g. virus vaccines, A61K39/00) · CPC title

  • Viruses as such, e.g. new isolates, mutants or their genomic sequences · CPC title

  • CpG containing adjuvants; Oligonucleotide containing adjuvants · CPC title

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What does patent US10098917B2 cover?
A parvovirus characterized by a CpG-enriched genome, wherein the genome contains at least 2 additional CpG inserts that are not present in the wild type genome is described as well as the use of said parvovirus, e.g., a parvovirus based on parvovirus H1, LuIII, Mouse minute virus (MMV), Mouse parvovirus (MPV), Rat minute virus (RMV), Rat parvovirus (RPV), Rat virus (RV), vectors based on the fo…
Who is the assignee on this patent?
Deutsches Krebsforschungszentrum Stiftung Des Oeffentlichen Rechts, Univ Heidelberg Ruprecht Karls, Univ Heidelberg Ruprecht Karls
What technology area does this patent fall under?
Primary CPC classification A61K35/768. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Oct 16 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).