Hiller Gregory W, Ovalle Ana Maria, Gagnon Matthew P, Curran Meredith L, Wang Wenge
Pfizer, Inc., 1 Burtt Road, Andover, Massachusetts, 01810.
Biotechnol Bioeng. 2017 Jul;114(7):1438-1447. doi: 10.1002/bit.26259. Epub 2017 Feb 9.
A simple method originally designed to control lactate accumulation in fed-batch cultures of Chinese Hamster Ovary (CHO) cells has been modified and extended to allow cells in culture to control their own rate of perfusion to precisely deliver nutritional requirements. The method allows for very fast expansion of cells to high density while using a minimal volume of concentrated perfusion medium. When the short-duration cell-controlled perfusion is performed in the production bioreactor and is immediately followed by a conventional fed-batch culture using highly concentrated feeds, the overall productivity of the culture is approximately doubled when compared with a highly optimized state-of-the-art fed-batch process. The technology was applied with near uniform success to five CHO cell processes producing five different humanized monoclonal antibodies. The increases in productivity were due to the increases in sustained viable cell densities. Biotechnol. Bioeng. 2017;114: 1438-1447. © 2017 Wiley Periodicals, Inc.
一种最初设计用于控制中国仓鼠卵巢(CHO)细胞补料分批培养中乳酸积累的简单方法已被改进和扩展,以使培养中的细胞能够控制自身的灌注速率,从而精确提供营养需求。该方法允许细胞非常快速地扩增至高密度,同时使用最少体积的浓缩灌注培养基。当在生产生物反应器中进行短时间的细胞控制灌注,并紧接着使用高浓度补料进行传统的补料分批培养时,与高度优化的先进补料分批工艺相比,培养物的整体生产力大约提高了一倍。该技术几乎成功地应用于五个生产五种不同人源化单克隆抗体的CHO细胞工艺。生产力的提高归因于持续活细胞密度的增加。《生物技术与生物工程》2017年;114: 1438 - 1447。© 2017威利期刊公司