IP Library Granted Patent US 9,238,063
Granted Patent B2
US 9,238,063 · App. 13/027,827 · Granted Jan 19, 2016

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

Inventors: Dolores Schendel (Munich, DE); Rudolf Wank (Munich, DE)
Assignee: Helmholtz Zentrum München Deutsches Forschungszentrum für Gesundlheit und Umwelt (GmbH)
A61K39/0011A61K48/00A61K2039/5154A61K2039/5156
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,238,063
App. No.
13/027,827
Granted
Jan 19, 2016
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 (9)

1. A method of treating a tumor disease 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, DNA, or cDNA encoding said proteins and/or peptides have been introduced, wherein said semi-allogeneic HLA-haploidentical antigen-presenting cells have class I and class II molecules in common with the patient, wherein said proteins and/or peptides are selected from proteins providing a growth advantage to the tumor and/or ensuring its survival, cell cycle regulatory proteins, transcription factors, and proteins involved in the regulation of cell division.

2. The method of claim 1 , wherein said proteins and/or peptides are selected from HER2/neu, PSMA, WT-1, mucins, or a telomerase.

3. The method of claim 2 , wherein the mucin is MUC-1.

4. The method of claim 3 , wherein said semi-allogeneic HLA-haploidentical antigen presenting cells are administered intravenously, subcutaneously, or intramuscularly.

5. The method of claim 1 , wherein two different semi-allogeneic donors are used to provide the semi-allogeneic HLA-haploidentical antigen presenting cells.

6. The method of claim 1 , wherein the semi-allogeneic HLA-haploidentical antigen presenting cells are monocytes, macrophages, or dendritic cells.

7. The method of claim 1 , wherein the semi-allogeneic HLA-haploidentical antigen presenting cells have HLA-A, -B, or -C molecules in common with the patient.

8. The method of claim 1 , wherein the semi-allogeneic HLA-haploidentical antigen presenting cells have HLA-DR, -DQ, or -DP molecules in common with the patient.

9. A method of treating a tumor disease 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, DNA, or cDNA encoding said proteins and/or peptides have been introduced, wherein said semi-allogeneic HLA-haploidentical antigen-presenting cells have class I and class II molecules in common with the patient, wherein said proteins and/or peptides are selected from proteins providing a growth advantage to the tumor and/or ensuring its survival, cell cycle regulatory proteins, transcription factors, and proteins involved in the regulation of cell division, wherein said RNA has been reverse transcribed from tumor cells derived from the patient into cDNA, the cDNA has been amplified by means of PCR, and subsequently the cDNA has been transcribed into RNA.

Priority Claims (1)
DE 101 12 851 · Mar 16, 2001 · national
Continuity (5)
Continuation 10665111 · Sep 16, 2003
Continuation 10663421 · Sep 15, 2003
Continuation PCTEP0202595 · Mar 8, 2002
Continuation PCTEP0202595
Related Publication 20110182945A1 · Jul 28, 2011