2021
DOI: 10.1016/j.crimmu.2021.03.002
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Hybridoma technology: is it still useful?

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Cited by 27 publications
(25 citation statements)
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“…16 However, the traditional antibodies have limitations including the unstable quality of pAbs caused by the batch-tobatch variation of immunized animals or the specificity loss of mAbs during thawing of hybridoma when it expressed additional functional variable regions. 17 Therefore, a novel type of antibody with more excellent characteristics would be urgently demanded.…”
Section: ■ Introductionmentioning
confidence: 99%
“…16 However, the traditional antibodies have limitations including the unstable quality of pAbs caused by the batch-tobatch variation of immunized animals or the specificity loss of mAbs during thawing of hybridoma when it expressed additional functional variable regions. 17 Therefore, a novel type of antibody with more excellent characteristics would be urgently demanded.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Despite the advent of many in vitro display technologies, the development of mAbs also relies on ex vivo single B cell interrogation (Box 1) [22,110]. Among the plethora of techniques enabling this process, the hybridoma technology is still used in new discovery pipelines because it is easy, cheap, and familiar to many scientists (Table 1).…”
Section: Discussionmentioning
confidence: 99%
“…Newer protocols accommodate several improvements, including some additional tissue culture measures such as the addition of cytokines and peritoneal macrophages to remove dead cells [20]. Some protocols also attempt to go beyond the PEG-based cell fusion step, implementing either electrofusion-based systems, or making use of fusogenic viruses such as Sendai virus or vesicular stomatitis virus to potentially increase the fusion efficiency between ASCs and myeloma cells, which represents one of the most relevant downsides of generating hybridomas [17,21,22].…”
Section: Glossarymentioning
confidence: 99%
“…Monoclonal antibody therapy has added great therapeutic value and enhanced the treatment efficacy for many diseases including cancer ( 106 ), infectious disease ( 107 ) and immunosuppression ( 108 ) in recent years. The credit to this success undeniably goes to the advances in technology such as hybridoma and phage display technology ( 109 ). The generated therapeutic monoclonal antibody is able to perform similar effector mechanisms as a typical human antibody which includes neutralization, activation of the complement cascade, antibody-dependent cellular cytotoxicity (ADCC) and antibody-dependent phagocytosis (ADP) ( 110 ).…”
Section: Antibody Therapymentioning
confidence: 99%