Therapeutic cancer vaccines derived from a novel dendritic cell line
The invention is in the field of medical sciences. It provides means and methods for the treatment of cancer. More in particular, it provides cells and cell lines that can be developed into fully functional dendritic cells. These cells endogenously express cancer-specific antigens, which makes them particularly suited for the treatment of different kinds of cancer. More in particular, the invention relates to a precursor cell line for dendritic cells called DC-One as deposited at the DSMZ under accession number DSMZ ACC3189 on Nov. 15, 2012.
1. A method for obtaining modified cells, the method comprising:
incubating a precursor cell line as deposited at the DSMZ under accession number DSMZ ACC3189 on Nov. 15, 2012, under conditions that allow differentiation of the precursor cells into immature cells; and
incubating the immature cells under conditions that allow maturation of the immature cells into modified cells, wherein the modified cells are CD34-positive, CD1a-positive, CD83-positive, and CD14-negative.
2. The method of claim 1 , further comprising altering the phenotype of the modified cells by introducing genetic material into the cells and/or by knocking out endogenous genes of the cells.
3. The method of claim 2 , wherein the genetic material is a gene encoding an immunotherapeutic agent.
4. The method of claim 3 , wherein the immunotherapeutic agent is selected from the group consisting of a tumor antigen, a viral antigen, and an antigen from a parasite, bacteria, or other microorganism.
5. The method of claim 1 , wherein conditions that allow differentiation of the precursor cells comprise contacting the precursor cells with a composition comprising at least one molecule selected from the group consisting of IL-4, IL-6, PGE-2, TNF-α, TGF-β, and GM-CSF.
6. The method of claim 5 , wherein differentiation of the precursor cells comprises contacting the precursor cells with a composition comprising GM-CSF, IL-4, and TNF-α.
7. The method of claim 1 , wherein conditions that allow maturation of the immature cells comprise contacting the immature cells with a composition comprising at least one molecule selected from the group consisting of IL-6, PGE-2, TNF-α, and IL1-β.
8. The method of claim 7 , wherein maturation of the immature cells comprises contacting the immature cells with a composition comprising TNF-α, PGE2, and IL1-β.
9. The method of claim 1 , further comprising combining the modified cell with a pharmaceutically acceptable carrier to form an immunogenic composition.
10. The method of claim 1 , further comprising loading the cell with at least one further antigen.
11. The method of claim 1 , further wherein the modified cells are CD40-positive, CD80-positive, and CD86-positive.
12. The method of claim 1 , wherein the precursor cell line is of leukemic origin.
13. A method for obtaining modified cells, the method comprising: differentiating a precursor cell line as deposited at the DSMZ under accession number DSMZ ACC3189 on Nov. 15, 2012, to produce modified cells, wherein the modified cells are CD34-positive, CD1a-positive, CD83-positive, and CD14-negative.
14. The method of claim 13 , further comprising combining the modified cell with a pharmaceutically acceptable carrier to form an immunogenic composition.
15. The method of claim 13 , further comprising loading the cell with at least one further antigen.
16. The method of claim 13 , further wherein the modified cells are CD40-positive, CD80-positive, and CD86-positive.
17. The method of claim 13 , wherein the precursor cell line is of leukemic origin.