Three-Dimensional Culture for Monoclonal Antibody Production by Hybridoma Cells Immobilized in Macroporous Gel Particles

被引:21
|
作者
Nilsang, Suthasinee [2 ,3 ,4 ]
Nehru, Vishal [1 ,2 ]
Plieva, Fatima M. [2 ,5 ]
Nandakumar, Kutty Selva [6 ]
Rakshit, Sudip Kumar [3 ]
Holmdahl, Rikard [6 ]
Mattiasson, Bo [2 ]
Kumar, Ashok [1 ]
机构
[1] Indian Inst Technol, Dept Biol Sci & Bioengn, Kanpur 208016, Uttar Pradesh, India
[2] Lund Univ, Ctr Chem & Chem Engn, Dept Biotechnol, SE-22100 Lund, Sweden
[3] Asian Inst Technol, Sch Environm Resources & Dev, Dept Food Engn & Bioproc Technol, Pathum Thani 12120, Thailand
[4] Valaya Alongkorn Rajabhat Univ, Fac Sci & Technol, Dept Biotechnol, Pathum Thani 12120, Thailand
[5] IDEON, Protista Biotechnol AB, SE-22370 Lund, Sweden
[6] Lund Univ, Sect Med Inflammat Research, Biomed Ctr, SE-22184 Lund, Sweden
基金
瑞典研究理事会;
关键词
antibody production; macroporous gel particles; M2139 hybridoma cells; 3D cultivation; cell immobilization; medium optimization;
D O I
10.1002/btpr.28
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
Cell proliferation and long-term production of monoclonal antibody IgG(2b) by M2139 hybridoma cells immobilized in macroporous gel particles (MGPs) in packed-bed reactor were studied for a period of 60 days. The MGPs were made of supermacroporous gels produced in frozen conditions from crosslinked polyacrylamide and modified with gelatin which were housed in special plastic carriers (7 x 9 mm(2)). Cells were trapped in the interior part of MGPs by attaching to the void space of the gel matrix as three-dimensional (3D) cultivation using gelatin as a substrate layer. Optimizing productivity by hybridoma cell relies on understanding regulation of antibody production. In this study, the behavior of M2139 cells in two-dimensional cultures on multiwell plate surfaces was also investigated. The effect of three different medium such as basal medium Dulbecco's modified Eagle's medium (D-MEM) containing L-glutamine or L-glutamine + 2 mM alpha-ketoglutarate or L-alanyl-glutamine (GlutaMAX (TM) ) was studied prior to its use in 3D cultivation. The kinetics of cell growth in basal medium containing L-glutamine + alpha-ketoglutarate was similar to cells grown on Gluta- MAX containing medium, whereas D-MEM containing L-glutamine showed lower productivity. With the maximal viable cell density (6.85 x 10(6) cells mL(-1)) and highest specific mAb production rate (3.9 mu g mL(-1) 10(-4) viable cell day(-1)), D-MEM-GlutaMAX was further selected for 3D cultivation. Cells in MGPs were able to grow and secrete antibody for 30 days in packed-bed batch reactor, before a fresh medium reservoir was replaced. After being supplied with fresh medium, cells again showed continuous growth for another 30 days with mAb production efficiency of 50%. These results demonstrate that MGPs can be used efficiently as supporting carrier for long-term monoclonal antibody production.
引用
收藏
页码:1122 / 1131
页数:10
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