Department of Cell Biology and Immunology, Intercollegiate Faculty of Biotechnology of UG nad MUG, Medical University of Gdańsk, Gdańsk, Poland.
Acta Biochim Pol. 2021 Aug 31;68(3):353-358. doi: 10.18388/abp.2020_5762.
Technical advances that lead to the era of targeted therapeutics demanded several milestones that were reached in the second half of the previous century. Professor Wacław Szybalski was the first one to perform a stable gene transfer in eukaryotic cells. To do so, he used his own designed system consisting of HPRT-deficient cells and HAT selective medium. Moreover, the first-ever hybridoma cells were also constructed by Wacław Szybalski's team. These spectacular achievements made him not only a forerunner of gene therapy, but also became a foundation for immunotherapy, as hybridoma and their selection by the HPRT-HAT system turned into a crucial technical step during production of monoclonal antibodies (mAbs). Herein, we present a story of anti-CD20 mAbs, one of the most successful lines of anticancer drugs. When looking back into history, the prototypic mAb rituximab was considered the biggest step forward in the therapy of B-cell malignancies. Nowadays, the second and third generations of anti-CD20 mAbs are approved in clinical use and numerous breakthrough studies on immune effector mechanisms were conducted with the aforementioned immunotherapeutics as a model.
技术进步使得靶向治疗时代成为可能,这需要在上个世纪后半叶达到几个里程碑。瓦乌拉斯·斯齐巴尔斯基教授是第一个在真核细胞中进行稳定基因转移的人。为此,他使用了自己设计的系统,该系统由 HPRT 缺陷细胞和 HAT 选择性培养基组成。此外,第一个杂交瘤细胞也是由瓦乌拉斯·斯齐巴尔斯基的团队构建的。这些卓越的成就使他不仅成为基因治疗的先驱,而且也成为免疫疗法的基础,因为杂交瘤及其通过 HPRT-HAT 系统的选择成为生产单克隆抗体 (mAb) 过程中的关键技术步骤。在这里,我们介绍了一种抗 CD20 mAb 的故事,这是最成功的抗癌药物之一。回顾历史,原型 mAb 利妥昔单抗被认为是 B 细胞恶性肿瘤治疗的最大进步。如今,第二代和第三代抗 CD20 mAb 已获准在临床使用,并且许多关于免疫效应机制的突破性研究都以上述免疫疗法为模型进行。