Kundu P K, Prasad N S, Datta D
School of Biomedical Engineering, Indian Institute of Technology-Bombay, India.
Indian J Exp Biol. 1998 Feb;36(2):125-35.
Getting higher yields of monoclonal antibody (MAb) is a problem in Hybridoma Technology which has two major bottlenecks--(a) poor yield of hybridized cells; and (b) low cellular productivity of MAb in culture. There are three ways of obtaining high MAb yield in vitro--(a) large scale culture of hybrid cells; (b) high density culture; and (c) enhancing individual cellular productivity in culture. Currently, focus is on correct synergistic combination of fortified nutrient media, bioreactor design and mode of operation. Maximisation of cell culture longevity, maintenance of high specific antibody secretion rates, nutrient supplementation, waste product minimization and control of environmental conditions are important parameters for improvement of large scale production of MAb. Though, MAb yield has enhanced rapidly over the decade, there is a growing concern for decrease in quality of MAb secreted. Further research is therefore necessary to take full advantage of MAb as a potential diagnostic agent for in vivo therapy.
获得更高产量的单克隆抗体(MAb)是杂交瘤技术中的一个问题,该技术存在两个主要瓶颈——(a)杂交细胞产量低;(b)培养物中MAb的细胞生产力低。在体外获得高MAb产量有三种方法——(a)杂交细胞的大规模培养;(b)高密度培养;(c)提高培养物中单个细胞的生产力。目前,重点在于强化营养培养基、生物反应器设计和操作模式的正确协同组合。细胞培养寿命的最大化、高特异性抗体分泌率的维持、营养补充、废物最小化以及环境条件的控制是提高MAb大规模生产的重要参数。尽管在过去十年中MAb产量迅速提高,但人们越来越担心所分泌MAb质量的下降。因此,有必要进行进一步研究,以充分利用MAb作为体内治疗的潜在诊断剂。