Department of Chemical Engineering, University of Almería, Almería, Spain.
Cytotechnology. 2013 Aug;65(4):655-62. doi: 10.1007/s10616-013-9593-z. Epub 2013 Jun 14.
The cell growth and monoclonal antibody production of the 55-6 hybridoma cell co-cultured with the murine thymoma cell line EL-4 at different initial 55-6:EL-4 ratios were investigated. Both populations were seeded in co-culture without previous stimulation and therefore with low constitutive CD40 and CD40 ligand (CD154) expression levels, and in the absence of exogenous co-stimuli. Viable cell density and growth rate data seem to suggest a competition for nutrients, which is detrimental for both cells in terms of biomass production and also of growth rate for 55-6. Final concentrations of antibody and specific antibody production rates were affected by the initial 55-6:EL-4 ratio. The 4:1 ratio yielded the highest IgG2a concentration, whereas the highest specific antibody production rate was obtained at the 2:1 ratio. Changes mainly in CD154 and also in CD40 expression in co-cultures could suggest cross-talk between both populations. In conclusion, different types of interactions are probably present in this co-culture system: competition for nutrients, cognate interaction and/or autocrine or paracrine interactions that influence the proliferation of both cells and the hybridoma antibody secretion. We are hereby presenting a pre-scale-up process that could speed up the optimization of large-scale monoclonal antibodies production in bioreactors by emulating the in vivo cell-cell interaction between B and T cells without previous stimulation or the addition of co-stimulatory molecules.
研究了不同初始 55-6:EL-4 比例下,55-6 杂交瘤细胞与小鼠胸腺瘤细胞系 EL-4 共培养时细胞生长和单克隆抗体产生的情况。两种细胞均未经预先刺激共培养,因此 CD40 和 CD40 配体(CD154)的组成性表达水平较低,且无外源共刺激物。活细胞密度和生长速率数据似乎表明存在营养物质竞争,这对两种细胞的生物量产生和 55-6 的生长速率都不利。抗体的最终浓度和特异性抗体产生速率受初始 55-6:EL-4 比例的影响。4:1 比例产生的 IgG2a 浓度最高,而 2:1 比例获得的特异性抗体产生速率最高。共培养物中 CD154 和 CD40 表达的变化可能表明两种细胞群之间存在串扰。总之,在这种共培养系统中可能存在不同类型的相互作用:营养物质竞争、同源相互作用和/或自分泌或旁分泌相互作用,影响两种细胞的增殖和杂交瘤抗体的分泌。我们在此介绍了一种预放大过程,通过模拟体内 B 和 T 细胞之间的细胞-细胞相互作用,无需预先刺激或添加共刺激分子,从而加速生物反应器中大规模单克隆抗体生产的优化。