The development of methods for obtaining monoclonal antibody-producing cells

被引:0
作者
Skowicki, Michal [1 ,2 ]
Lipinski, Tomasz [1 ,2 ]
机构
[1] Inst Immunol & Terapii Doswiadczalnej PAN L Hirsz, Ul R Weigla 12, PL-53114 Wroclaw, Poland
[2] Wroclawskie Ctr Badan EIT, Wroclaw, Poland
来源
POSTEPY HIGIENY I MEDYCYNY DOSWIADCZALNEJ | 2016年 / 70卷
关键词
monoclonal antibodies; hybridoma; cell fusion; clone selection; ASCITES TUMOR-FORMATION; SURFACE EXPRESSION; ANTIGEN RECEPTOR; HYBRIDOMA CELLS; PLASMID DNA; FUSION; GEL; IMMUNIZATION; IMMUNOGLOBULIN; FLUORESCENCE;
D O I
10.5604/17322693.1200552
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Monoclonal antibodies (mAbs) are biomolecules of great scientific and practical significance. In contrast to polyclonal antibodies from immune sera, they are homogeneous and monospecific, since they are produced by hybridoma cells representing a clone arising from a single cell. The successful technology was described for the first time in 1975; the inventors were later awarded the Nobel Prize. Currently, mAbs are broadly used as a research tool, in diagnostics and medicine in particular for the treatment of cancer or in transplantology. About 47 therapeutics based on monoclonal antibodies are now available in the US and Europe, and the number is still growing. Production of monoclonal antibodies is a multistage, time-consuming and costly process. Growing demand for these molecules creates space for research focused on improvements in hybridoma technology. Lower costs, human labor, and time are important goals of these attempts. In this article, a brief review of current methods and their advances is given.
引用
收藏
页码:367 / 379
页数:13
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