Microcarrier perfusion culturing methods and uses thereof
Provided herein are methods of culturing an adherent mammalian cell in a shake tube using a plurality of microcarriers and batch re-feed perfusion, and various methods that utilize these culturing methods.
1. A method of culturing an adherent Chinese hamster ovary (CHO) cell, the method comprising:
providing a conical shake tube containing an adherent CHO cell disposed in a first liquid culture medium, wherein the first liquid culture medium occupies about 10% to about 30% of the volume of the conical shake tube and contains a plurality of microcarriers at a concentration of about 1.0 g/L to about 15.0 g/L, wherein the microcarriers have (1) an average diameter of about 200 Tm to about 300 Tm and (2) a plurality of pores, wherein the plurality of pores have an average diameter of about 25 μm to about 35 μm;
incubating the conical shake tube for a period of time at about 32° C. to about 39° C. with a rotary agitation of about 130 revolutions per minute (RPM) to about 150 RPM; and
after about the first 48 to 96 hours of the period of time, continuously or periodically removing a first volume of the first liquid culture medium and adding to the first liquid culture medium a second volume of a second liquid culture medium, wherein the first and second volumes are about equal, and the method achieves a viable cell density of greater than 2.0×10 6 cells/mL in the first liquid culture medium or a combination of the first and second liquid culture medium at some point during the period of time.
2. The method of claim 1 , wherein the adherent CHO cell contains a nucleic acid encoding a recombinant protein.
3. The method of claim 2 , further comprising:
recovering the recombinant protein from the adherent CHO cell or from the first and/or second liquid culture medium.
4. The method of claim 2 , further comprising:
detecting the recombinant protein in the adherent CHO cell or in the first and/or second culture medium; and
comparing the amount of recombinant protein present in the adherent CHO cell or in the first and/or second culture medium to a reference level of recombinant protein.
5. The method of claim 4 , wherein the reference level of recombinant protein is a level of recombinant protein produced using a different culturing method.
6. The method of claim 2 , further comprising:
detecting the recombinant protein in the adherent CHO cell or in the first and/or second culture medium;
comparing the amount of recombinant protein present in the adherent CHO cell or in the first and/or second culture medium to a reference level of recombinant protein produced by a different method that uses one or more of a different first or second liquid culture medium, a different raw ingredient or supplement present in the first or second liquid culture medium, or a different source of an adherent CHO cell; and
identifying the first or second liquid culture medium, the raw ingredient or supplement present in the first or second liquid culture medium, or the source of the adherent CHO cell that is associated with an increased amount of recombinant protein as compared to the reference level as being efficacious for use in a method of producing a recombinant protein.
7. The method of claim 2 , further comprising:
detecting the recombinant protein in the adherent CHO cell or in the first and/or second culture medium;
comparing the amount of recombinant protein present in the adherent CHO cell or in the first and/or second culture medium to a reference level of recombinant protein produced by a different method; and
identifying and removing or altering in a manufacturing process any culture components or parameters that are associated with a decrease in the amount of recombinant protein produced as compared to the reference level, or identifying and adding to a manufacturing process any culture components or parameters that are associated with an increase in the amount of recombinant protein produced as compared to the reference level.
8. The method of claim 1 , wherein the removing of the first volume of the first liquid culture medium and the adding of the second volume of the second liquid culture medium is performed periodically.
9. The method of claim 1 , wherein the first volume of the first liquid culture medium removed and the second volume of the second liquid culture medium added are increased over time.
10. The method of claim 1 , wherein:
the conical shake tube has a volume of between about 10 mL to about 100 mL; or
the adherent CHO cell is suspended in about 2 mL to about 20 mL of the first liquid culture medium.
11. The method of claim 1 , wherein after about the first 48 to 96 hours of the period of time, in each 24-hour period, the first volume of the first liquid culture medium removed and the second volume of the second liquid culture medium added is about 30% to about 95% of the volume of the first liquid culture medium.
12. The method of claim 1 , wherein the conical shake tube is incubated at a reactor angle of about 25 degrees to about 90 degrees from horizontal.
13. The method of claim 1 , wherein the plurality of microcarriers are at a final concentration of about 1.0 g/L to about 2.0 g/L in the conical shake tube.
14. A method of culturing an adherent CHO cell, the method comprising:
(a) providing a conical shake tube containing an adherent CHO cell disposed in a first liquid culture medium that occupies about 10% to about 30% of the volume of the conical shake tube and contains a plurality of microcarriers in a concentration of about 1.0 g/L to about 15.0 g/L, wherein the microcarriers have (1) an average diameter of about 200 Tm to about 300 Tm and (2) a plurality of pores, wherein the plurality of pores have an average diameter of about 25 μm to about 35 μm;
(b) incubating the conical shake tube for a first time period at about 35° C. to about 39° C. with a rotary agitation of about 130 revolutions per minute (RPM) to about 150 RPM, and after about the first 48 to 96 hours of the first period of time, in each subsequent 24-hour period,
(i) continuously or periodically removing a first volume of the first liquid culture medium that is substantially free of microcarriers from the conical shake tube, wherein the first volume is about 10% to about 95% of the volume of the first liquid culture medium; and
(ii) adding to the conical shake tube a second volume of a second liquid culture medium, wherein the first and second volumes are about equal;
(c) incubating the conical shake tube after the cell concentration reaches about target cell density for a second time period of about 2 days to about 7 days, at about 32° C. to about 39° C. with the rotary agitation, and in each 24-hour period, performing steps (b)(i) and (b)(ii), wherein the first and second liquid culture media used in step (b) are of a substantially different type from those used in step (c); and
(d) incubating the conical shake tube for a third time period greater than 2 days, at about 35° C. to about 39° C. with the rotary agitation, and in each 24-hour period, performing steps (b)(i) and (b)(ii), wherein the first and second liquid culture media used in step (c) are of the same type as those used in step (d).
15. The method of claim 14 , wherein the adherent CHO cell contains a nucleic acid encoding a recombinant protein.
16. The method of claim 15 , further comprising:
(e) recovering the recombinant protein from the adherent CHO cell or the first and/or second liquid culture medium used during the first, second, and/or third period of time.
17. The method of claim 14 , wherein the removing of the first volume of the first liquid culture medium, and the adding of the second volume of the second liquid culture medium in one of more of the first time period, the second time period, and the third time period is performed periodically.
18. The method of claim 14 , wherein:
the shake tube has a volume of between about 10 mL to about 100 mL; or
the volume of the first culture medium is about 2 mL to about 20 mL.
19. The method of claim 14 , wherein the first volume of the first liquid culture medium removed and the second volume of the second liquid culture medium added in one or more of the first time period, the second time period, and the third time period is about 70% of the volume of the first liquid culture medium.
20. The method of claim 14 , wherein the conical shake tube is incubated in (b), (c), and (d) at a reactor angle of about 25 degrees to about 90 degrees from horizontal.
21. A method of testing for the presence of a contaminant in a first or second liquid culture medium, a raw material used to generate a first or second liquid culture medium, or a source of an adherent CHO cell, the method comprising:
providing a conical shake tube containing an adherent CHO cell disposed in a first liquid culture medium, wherein the first liquid culture medium occupies about 10% to about 30% of the volume of the conical shake tube and contains a plurality of microcarriers at a concentration of about 1.0 g/L to about 15.0 g/L, wherein the microcarriers have (1) an average diameter of about 200 Tm to about 300 Tm and (2) a plurality of pores, wherein the plurality of pores have an average diameter of about 25 μm to about 35 μm;
incubating the conical shake tube for a period of time at about 32° C. to about 39° C. and with a rotary agitation of about 130 revolutions per minute (RPM) to about 150 RPM; and
after about the first 48 to 96 hours of the period of time, continuously or periodically removing a first volume of the first liquid culture medium and adding to the first liquid culture medium a second volume of a second liquid culture medium, wherein the first and second volumes are about equal;
detecting the recombinant protein in the adherent CHO cell or in the first and/or second culture medium;
comparing the amount of recombinant protein present in the adherent CHO cell or in the first and/or second culture medium to a reference level of recombinant protein produced by a different method that uses one or more of a different first or second liquid culture medium, a different raw material to generate the first or second liquid culture medium, or a different source of the adherent CHO cell; and
identifying the first or second liquid culture medium, the raw material used to generate the first or second liquid culture medium, or the source of an adherent CHO cell as containing a contaminant when the level of recombinant protein produced is less than the reference level.