Process for the culturing of cells
The invention relates to a process for the culturing of cells, preferably E1-immortalized HER cells, more preferably PER.C6 cells in a reactor in suspension in a cell culture medium, wherein the cells produce a biological substance, preferably an antibody, wherein at least one cell culture medium component is fed to the cell culture and wherein the cell culture comprising the cells, the biological substance and cell culture medium is circulated over a separation system and wherein the separation system separates the biological substance from substances having a lower molecular weight than the biological substance and wherein the biological substance is retained in or fed back into the reactor. Preferably part of the substances of lower molecular weight is continuously removed from the cell culture.
1. Process for the culturing of cells in a reactor in suspension in a cell culture medium, comprising:
circulating a cell culture through a separation system,
wherein the cell culture comprises eukaryotic cells, a biological substance produced by the cells, and a cell culture medium;
wherein the biological substance is an IgG;
wherein at least one cell culture medium component is fed to the cell culture;
wherein the cell culture is circulated through the separation system in a flow substantially parallel to a surface of said separation system resulting in a liquid outflow and a flow wherein cell culture contents are retained or fed back into the reactor;
wherein the separation system comprises a filter having a pore size characterized by a molecular weight cut-off smaller than the molecular weight of the biological substance to separate the biological substance from substances having a lower molecular weight than the biological substance;
wherein the liquid outflow consists essentially of components having molecular weight lower than that of the biological substance and the flow wherein cell culture contents are retained or fed back into the reactor consists essentially of components having molecular weight equal to or higher than that of the biological substance;
wherein the cell culture is removed at least once from the reactor, and
wherein the biological substance is harvested from the cells and/or from the cell culture.
2. Process according to claim 1 , wherein the filter comprises a membrane filter.
3. Process according to 2 , wherein the membrane filter comprises a hollow fiber filter.
4. Process according to claim 2 or 3 wherein the filter has a pore size with a molecular weight cut-off of at most 100 kDa.
5. Process according to claim 4 , wherein the filter has a pore size with a molecular weight cut-off of at most 50 kDa.
6. Process according to claim 5 , wherein the filter has a pore size with a molecular weight cut-off of at most 30 kDa.
7. Process according to claim 1 , wherein the molecular weight cut-off is smaller by at least a factor of 2 than the molecular weight of the IgG.
8. Process according to claim 1 , wherein the molecular weight cut-off is smaller by at least a factor of 3 than the molecular weight of the IgG.
9. Process according to claim 1 wherein the cell culture is circulated through the filter in an alternating tangential flow.
10. Process according to claim 1 wherein the cell culture is circulated through the filter in a unidirectional tangential flow.
11. Process according to claim 1 , wherein part of the substances of lower molecular weight is continuously removed from the cell culture.
12. Process according to claim 1 , wherein the cells are mammalian cells.
13. Process according to claim 12 , wherein the mammalian cells are selected from the group consisting of Chinese hamster ovary (CHO) cells, hybridomas, baby hamster kidney (BHK) cells, myeloma cells, human cells, or mouse cells.
14. Process according to claim 13 , wherein the mammalian cells are Chinese hamster ovary (CHO) cells.
15. Process according to claim 1 , wherein the harvesting comprises subjecting the cell culture to affinity chromatography and/or ion exchange chromatography.