IP Library Granted Patent US 8,206,701
Granted Patent B2
US 8,206,701 · App. 10/665,111 · Granted Jun 26, 2012

Semi-allogenic anti-tumour vaccine with HLA haplo-identical antigen-presenting cells

Assignee: Helmholtz Zentrum München Deutsches Forschungszentrum für Gesundheit und Umwelt (GmbH)
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Quick Facts
Patent No.
US 8,206,701
App. No.
10/665,111
Granted
Jun 26, 2012
Kind
B2
Abstract

The present invention relates to semi-allogeneic antigen-presenting cells into which proteins and/or peptides or RNA or DNA or cDNA, respectively, encoding said proteins and/or peptides which are overexpressed in tumor cells or which are derived from autologous tumor cells or different tumor cells or different tumor cell lines have been introduced. Furthermore the invention relates to methods for the generation of these semi-allogeneic antigen-presenting cells as well as to the use thereof in the treatment of tumor diseases.

Claims (10)

1. A method for the generation of HLA-haploidentical antigen-presenting cells for the treatment of tumor diseases in a patient comprising the following steps:

providing a patient to be treated;

providing antigen-presenting cells from a semi-allogeneic donor which are HLA-haploidentical with respect to those of the patient, wherein HLA-haploidentical antigen-presenting cells have class I and class II molecules in common with the patient; and

introducing proteins and/or peptides or RNA or DNA or cDNA encoding said proteins and/or peptides into the HLA-haploidentical antigen-presenting cells, wherein said proteins and/or peptides are tumor-defined antigens or wherein said RNA or DNA or cDNA encodes tumor-defined antigens, wherein the tumor-defined antigens are antigens overexpressed in the tumor cells, wherein the tumor-defined antigens are selected from the group consisting of oncogenes, proteins providing a growth advantage to the tumor and/or ensuring its survival, cell cycle regulatory proteins, transcription factors, mucins, and proteins involved in the regulation of cell division.

2. A method for the generation of HLA-haploidentical antigen presenting cells for the treatment of tumor diseases in a patient comprising the following steps:

providing a patient to be treated;

providing antigen-presenting cells from a semi-allogeneic donor which are HLA-haploidentical with respect to those of the patient, wherein HLA-haploidentical antigen-presenting cells have class I and class II molecules in common with the patient, wherein antigen-presenting cells of two different HLA-haploidentical individuals are used; and

introducing proteins and/or peptides or RNA or DNA or cDNA encoding said proteins and/or peptides into the HLA-haploidentical antigen-presenting cells, wherein said proteins and/or peptides are tumor-defined antigens or wherein said RNA or DNA or cDNA encodes tumor-defined antigens, wherein the tumor-defined antigens are antigens overexpressed in the tumor cells, wherein the tumor-defined antigens are selected from the group consisting of oncogenes, proteins providing a growth advantage to the tumor and/or ensuring its survival, cell cycle regulatory proteins, transcription factors, mucins, and proteins involved in the regulation of cell division.

3. A method of treatment of tumor diseases in a patient comprising administering to said patient a therapeutically effective amount of semi-allogeneic HLA-haploidentical antigen presenting cells into which proteins and/or peptides or RNA or DNA or cDNA encoding said proteins and/or peptides have been introduced, wherein HLA-haploidentical antigen-presenting cells have class I and class II molecules in common with the patient, and wherein said proteins and/or peptides are overexpressed in tumor cells or derived from autologous tumor cells, and wherein said HLA-haploidentical antigen-presenting cells are administered by the intravenous, subcutaneous or intramuscular route.

4. A method of treatment of tumor diseases in a patient comprising administering to said patient a therapeutically effective amount of semi-allogeneic HLA-haploidentical antigen presenting cells into which proteins and/or peptides or RNA or DNA or cDNA encoding said proteins and/or peptides have been introduced, wherein HLA-haploidentical antigen-presenting cells have class I and class II molecules in common with the patient, wherein HLA-haploidentical antigen-presenting cells of two different HLA-haploidentical individuals are used; and wherein said proteins and/or peptides are overexpressed in tumor cells or derived from autologous tumor cells, and wherein said HLA-haploidentical antigen-presenting cells are administered by the intravenous, subcutaneous or intramuscular route.

Assignments (2)
CHANGE OF NAME Recorded Nov 19, 2010
From: GSF - FORSCHUNGSZENTRUM FUR UMWELT UND GESUNDHEIT, GMBH
To: HELMHOLTZ ZENTRUM MUNCHEN DEUTSCHES FORSCHUNGSZENTRUM FUR GESUNDHEIT UND UMWELT (GMBH)
Reel/Frame 025310/0964 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2004
From: SCHENDEL, DOLORES; WANK, RUDOLF
To: GSF-FORSCHUNGSZENTRUM FUR UMWELT UND GESUNDHEIT GMBH
Reel/Frame 014597/0082 →
Continuity (5)
Continuation 10663421 · Sep 15, 2003
Continuation PCTEP0202595 · Mar 8, 2002
Continuation 10665111
Continuation PCTEP0202595
Related Publication 20050175596A1 · Aug 11, 2005