Methods of adenovirus production
View Patent ↗A simple yet effective method of increasing production of a thermo-stable virus, such as adenovirus and picornavirus, is presented. The method entails a temperature shift strategy whereby the culture of host cells are shifted to a sub-optimal temperature for a period of time prior to virus infection or cells are grown at a sub-optimal level for the entire cell expansion process including one or more than one passages of cell growth from cryopreserved cells, followed by a shift back to a more optimal temperature at or near the time of virus infection of the respective host cells. Adaptation of such a temperature shift strategy present a simple yet effective method to substantially increase recoverable virus within a respective host cell/virus production scheme without the need to further manipulate other culture and/or media conditions within an established host cell/virus production scheme.
1. A method of producing adenovirus, comprising:
a) culturing host cells at a temperature from 31° C. to 34° C.;
b) infecting the host cells with an adenovirus, resulting in adenovirus-infected host cells;
c) culturing the adenovirus-infected host cells at a temperature from 35° C. to 38° C.;
d) harvesting adenovirus and/or cells containing adenovirus from the culture; and,
e) purifying adenovirus away from host cell and culture contaminants, resulting in a purified adenovirus product.
2. A method of producing adenovirus, comprising:
a) inoculating and culturing host cells in an appropriate medium at a temperature from 35° C. to 38° C.;
b) shifting the temperature of the host cell culture of step a) to a temperature from 31° C. to 34° C.;
c) infecting the host cells of step b) with a adenovirus, resulting in adenovirus-infected host cells;
d) culturing the adenovirus-infected host cells at a temperature from 35° C. to 38° C.;
e) harvesting adenovirus and/or cells containing adenovirus from the culture; and,
f) purifying adenovirus away from host cell and culture contaminants, resulting in a purified adenovirus product.
3. A method according to claim 2 wherein the culture temperature in step b) is lowered to a temperature from 31° C. to 34° C. for up to the entire cell passages prior to infecting the host cells with the adenovirus.
4. A method according to claim 2 wherein the culture temperature in step b) is lowered to a temperature from 31° C. to 34° C. for at least 24 hours prior to infecting the host cells with the adenovirus.
5. A method according to claim 3 wherein the temperature for cell growth in step a) is from 36° C. to 38° C.
6. A method according to claim 4 wherein the temperature for cell growth in step a) is from 36° C. to 38° C.
7. A method according to claim 3 wherein the temperature for cell growth in step a) is from 36° C. to 38° C. and the temperature for growth of infected host cells of step c) is from 36° C. to 38° C.
8. A method according to claim 4 wherein the temperature for cell growth in step a) is from 36° C. to 38° C. and the temperature for growth of infected host cells of step c) is from 36° C. to 38° C.