Gavrilov-Yusim Natalie, Hahiashvili Ekaterina, Tashker Marina, Yavelsky Victoria, Karnieli Ohad, Lobel Leslie
Department of Virology and Developmental Genetics, Ben Gurion University of the Negev, Beersheva 84105, Israel.
BMC Biotechnol. 2008 Jan 14;8:3. doi: 10.1186/1472-6750-8-3.
The isolation and production of human monoclonal antibodies is becoming an increasingly important pursuit as biopharmaceutical companies migrate their drug pipelines away from small organic molecules. As such, optimization of monoclonal antibody technologies is important, as this is becoming the new rate-limiting step for discovery and development of new pharmaceuticals. The major limitations of this system are the efficiency of isolating hybridoma clones, the process of stabilizing these clones and optimization of hybridoma cell secretion, especially for large-scale production. Many previous studies have demonstrated how perturbations in the aqueous environment can impact upon cell biology. In particular, radio frequency (RF) irradiation of solutions can have dramatic effects on behavior of solutions, cells and in particular membrane proteins, although this effect decays following removal of the RF. Recently, it was shown that nanoparticle doping of RF irradiated water (NPD water) produced a stabilized aqueous medium that maintained the characteristic properties of RF irradiated water for extended periods of time. Therefore, the ordering effect in water of the RF irradiation can now be studied in systems that required prolonged periods for analysis, such as eukaryotic cell culture. Since the formation of hybridoma cells involves the formation of a new membrane, a process that is affected by the surrounding aqueous environment, we tested these nanoparticle doped aqueous media formulations on hybridoma cell production.
In this study, we tested the entire process of isolation and production of human monoclonal antibodies in NPD water as a means for further enhancing human monoclonal antibody isolation and production. Our results indicate an overall enhancement of hybridoma yield, viability, clonability and secretion. Furthermore, we have demonstrated that immortal cells proliferate faster whereas primary human fibroblasts proliferate slower in NPD water.
Overall, these studies indicate that NPD water can enhance cell proliferation, clonability and secretion. Furthermore, the results support the hypothesis that NPD water is effectively composed of stable microenvironments.
随着生物制药公司将其药物研发管线从小有机分子转向其他领域,人源单克隆抗体的分离与生产正变得愈发重要。因此,单克隆抗体技术的优化至关重要,因为这正成为新药物发现与开发的新限速步骤。该系统的主要局限性在于杂交瘤克隆的分离效率、这些克隆的稳定过程以及杂交瘤细胞分泌的优化,尤其是在大规模生产方面。此前许多研究已证明水环境中的扰动如何影响细胞生物学。特别是,溶液的射频(RF)照射可对溶液、细胞尤其是膜蛋白的行为产生显著影响,尽管在去除射频后这种影响会衰减。最近,研究表明对射频照射水进行纳米颗粒掺杂(NPD水)可产生一种稳定的水介质,该介质能长时间保持射频照射水的特性。因此,现在可以在需要长时间分析的系统(如真核细胞培养)中研究射频照射在水中的有序效应。由于杂交瘤细胞的形成涉及新膜的形成,而这一过程会受到周围水环境的影响,我们在杂交瘤细胞生产中测试了这些纳米颗粒掺杂的水介质配方。
在本研究中,我们测试了在NPD水中人源单克隆抗体的整个分离与生产过程,以此作为进一步提高人源单克隆抗体分离与生产的一种方法。我们的结果表明杂交瘤的产量、活力、克隆能力和分泌能力总体上有所提高。此外,我们已证明永生细胞在NPD水中增殖更快,而原代人成纤维细胞增殖更慢。
总体而言,这些研究表明NPD水可增强细胞增殖、克隆能力和分泌能力。此外,结果支持了NPD水有效由稳定微环境组成的假设。