MDCK suspension cell lines in serum-free, chemically-defined media for vaccine production
Disclosed is an adapted Madin-Darby canine kidney cell line capable of suspension culture in the absence of serum, and a chemically-defined medium for culture of the adapted MDCK cell line. Further disclosed are culture methods for growing the adapted MDCK cell line and methods for producing a vaccine from the adapted MDCK cell line grown in the chemically-defined medium.
1. A composition comprising adapted Madin-Darby canine kidney (MDCK) cells and a growth medium, the growth medium comprising a chemically-defined and animal component free medium, wherein the adapted MDCK cells are in suspension culture without microcarriers, wherein the chemically defined medium sustains cell growth and expansion without medium exchange or subculture, further wherein the adapted MDCK cells are deposited as DSM ACC3309 with Leibniz-Institut DSMZ-Deutsche Sammlung von Mikro-organismen and Zellkulturen GmbH.
2. The composition of claim 1 , wherein the adapted MDCK cells have an average doubling time of between about 30 hours and about 35 hours.
3. The composition of claim 1 , wherein the adapted MDCK cells are suitable for producing a virus for a vaccine, further wherein the virus maintains antigenicity.
4. A method for producing a virus for vaccine production in adapted Madin-Darby canine kidney (MDCK) cells, said adapted MDCK cells being capable of being cultured in suspension without microcarriers, said method comprising contacting the adapted MDCK cells with a chemically-defined and animal component free growth medium, infecting the cells with a virus, and harvesting the virus, wherein the chemically defined medium sustains cell growth and expansion without medium exchange or subculture, and further wherein the adapted MDCK cells are deposited as DSM ACC3309 with Leibniz-Institut DSMZ-Deutsche Sammlung von Mikro-organismen and Zellkulturen GmbH.
5. A method for producing Madin-Darby canine kidney (MDCK) cells that are capable of being cultured in suspension without microcarriers in a chemically-defined medium without serum, said method comprising:
a) providing adherent MDCK cells;
b) culturing the adherent MDCK cells in a growth medium comprising serum in a stirred bioreactor and in the absence of microcarriers for a period of time sufficient for the MDCK cells to adapt to suspension culture; and
c) culturing the suspension-adapted MDCK cells in suspension culture in a chemically-defined medium and without serum, thereby providing MDCK cells that are capable of being cultured in suspension without microcarriers in a chemically-defined medium without serum,
wherein the chemically defined medium sustains cell growth and expansion without medium exchange or subculture, further wherein the adapted MDCK cells are deposited as DSM ACC3309 with Leibniz-Institut DSMZ-Deutsche Sammlung von Mikro-organismen and Zellkulturen GmbH.
6. The method of claim 5 , wherein the growth medium comprises between about 1% and about 10% serum.
7. The method of claim 6 , wherein the growth medium comprises about 5% serum.
8. The method of claim 5 , wherein the MDCK cells are cultured in the presence of 5% CO 2 in steps b) and c).
9. The method of claim 5 , wherein the adapted MDCK cells have an average doubling time of between about 30 hours and about 35 hours.
10. The method of claim 5 , wherein the adapted MDCK cells are suitable for producing virus for a human vaccine, further wherein a virus is produced and the virus maintains antigenicity.
11. A composition comprising adapted MDCK cells produced by the method of claim 5 .
12. The composition of claim 11 , wherein the adapted MDCK cells have an average doubling time of between about 30 hours and about 35 hours.
13. The composition of claim 11 , wherein the adapted MDCK cells are suitable for producing virus for a human vaccine, further wherein the virus maintains antigenicity.