Scaled-up Manufacturing of Recombinant Antibodies Produced by Plant Cells in a 200-L Orbitally-Shaken Disposable Bioreactor

被引:63
作者
Raven, Nicole [1 ]
Rasche, Stefan [1 ]
Kuehn, Christoph [1 ]
Anderlei, Tibor [2 ]
Kloeckner, Wolf [3 ]
Schuster, Flora [4 ]
Henquet, Maurice [5 ]
Bosch, Dirk [5 ,6 ]
Buechs, Jochen [7 ]
Fischer, Rainer [1 ,4 ]
Schillberg, Stefan [1 ,8 ]
机构
[1] Fraunhofer Inst Mol Biol & Appl Ecol IME, D-52074 Aachen, Germany
[2] Adolf Kuhner AG, CH-4127 Birsfelden, Switzerland
[3] Bayer Technol Serv, D-51368 Leverkusen, Germany
[4] Rhein Westfal TH Aachen, Inst Mol Biotechnol, D-52074 Aachen, Germany
[5] Plant Res Int, PRI Biosci, NL-6700 AP Wageningen, Netherlands
[6] Univ Utrecht, Dept Membrane Biochem & Biophys, NL-3584 CH Utrecht, Netherlands
[7] Rhein Westfal TH Aachen, AVT Biochem Engn, D-52074 Aachen, Germany
[8] Univ Giessen, Inst Phytopathol & Appl Zool, Dept Phytopathol, D-35392 Giessen, Germany
关键词
antibody purification; expanded bed chromatography; Nicotiana tabacum Bright Yellow 2 (BY-2); plant cell suspension culture; scaled-up manufacture; single-use technology; EXPANDED-BED ADSORPTION; ENZYME REPLACEMENT THERAPY; HIGH-YIELD PRODUCTION; PHARMACEUTICAL PROTEINS; MONOCLONAL-ANTIBODY; FOREIGN PROTEINS; CHO-CELLS; PURIFICATION; CULTURE; TECHNOLOGY;
D O I
10.1002/bit.25352
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Tobacco BY-2 cells have emerged as a promising platform for the manufacture of biopharmaceutical proteins, offering efficient protein secretion, favourable growth characteristics and cultivation in containment under a controlled environment. The cultivation of BY-2 cells in disposable bioreactors is a useful alternative to conventional stainless steel stirred-tank reactors, and orbitally-shaken bioreactors could provide further advantages such as simple bag geometry, scalability and predictable process settings. We carried out a scale-up study, using a 200-L orbitally-shaken bioreactor holding disposable bags, and BY-2 cells producing the human monoclonal antibody M12. We found that cell growth and recombinant protein accumulation were comparable to standard shake flask cultivation, despite a 200-fold difference in cultivation volume. Final cell fresh weights of 300-387 g/L and M12 yields of similar to 20 mg/L were achieved with both cultivation methods. Furthermore, we established an efficient downstream process for the recovery of M12 from the culture broth. The viscous spent medium prevented clarification using filtration devices, but we used expanded bed adsorption (EBA) chromatography with SP Sepharose as an alternative for the efficient capture of the M12 antibody. EBA was introduced as an initial purification step prior to protein A affinity chromatography, resulting in an overall M12 recovery of 75-85% and a purity of >95%. Our results demonstrate the suitability of orbitally-shaken bioreactors for the scaled-up cultivation of plant cell suspension cultures and provide a strategy for the efficient purification of antibodies from the BY-2 culture medium. (C) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:308 / 321
页数:14
相关论文
共 84 条
[1]   HIGH-EFFICIENCY TRANSFORMATION OF CULTURED TOBACCO CELLS [J].
AN, GH .
PLANT PHYSIOLOGY, 1985, 79 (02) :568-570
[2]  
[Anonymous], BIOPROCESS INT
[3]   Expanded-bed chromatography in primary protein purification [J].
Anspach, FB ;
Curbelo, D ;
Hartmann, R ;
Garke, G ;
Deckwer, WD .
JOURNAL OF CHROMATOGRAPHY A, 1999, 865 (1-2) :129-144
[4]  
Batt Brian C., 1995, Bioseparation, V5, P41
[5]   Direct coupling of expanded bed adsorption with a downstream purification step [J].
Beck, JT ;
Williamson, B ;
Tipton, B .
BIOSEPARATION, 1999, 8 (1-5) :201-207
[6]   Rapid, high-yield production in plants of individualized idiotype vaccines for non-Hodgkin's lymphoma [J].
Bendandi, M. ;
Marillonnet, S. ;
Kandzia, R. ;
Thieme, F. ;
Nickstadt, A. ;
Herz, S. ;
Froede, R. ;
Inoges, S. ;
Lopez-Diaz de Cerio, A. ;
Soria, E. ;
Villanueva, H. ;
Vancanneyt, G. ;
McCormick, A. ;
Tuse, D. ;
Lenz, J. ;
Butler-Ransohoff, J. -E. ;
Klimyuk, V. ;
Gleba, Y. .
ANNALS OF ONCOLOGY, 2010, 21 (12) :2420-2427
[7]   A CHIMAERIC ANTIBIOTIC-RESISTANCE GENE AS A SELECTABLE MARKER FOR PLANT-CELL TRANSFORMATION [J].
BEVAN, MW ;
FLAVELL, RB ;
CHILTON, MD .
NATURE, 1983, 304 (5922) :184-187
[8]   Expanded bed adsorption in the purification of monoclonal antibodies: a comparison of process alternatives [J].
Blank, GS ;
Zapata, G ;
Fahrner, R ;
Milton, M ;
Yedinak, C ;
Knudsen, H ;
Schmelzer, C .
BIOSEPARATION, 2001, 10 (1-3) :65-71
[9]   Activated vitronectin as a target for anticancer therapy with human antibodies [J].
Bloemendal, HJ ;
de Boer, HC ;
Koop, EA ;
van Dongen, AJ ;
Goldschmeding, R ;
Landman, WJM ;
Logtenberg, T ;
Gebbink, MFBG ;
Voest, EE .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2004, 53 (09) :799-808
[10]   N-Glycosylation of Plant-produced Recombinant Proteins [J].
Bosch, Dirk ;
Castilho, Alexandra ;
Loos, Andreas ;
Schots, Arjen ;
Steinkellner, Herta .
CURRENT PHARMACEUTICAL DESIGN, 2013, 19 (31) :5503-5512