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用于先导治疗性抗体早期发现与开发的植物表达系统。

Plant expression systems for early stage discovery and development of lead therapeutic antibodies.

作者信息

Virdi Vikram, Juarez Paloma, Depicker Ann

机构信息

Department of Plant Systems Biology, VIB, Ghent, Belgium.

Department of Plant Biotechnology and Bioinformatics, Ghent University, Ghent, Belgium.

出版信息

Hum Antibodies. 2015 Dec 23;23(3-4):37-43. doi: 10.3233/HAB-150285.

Abstract

BACKGROUND

Antibodies for human clinical applications are predominantly produced in mammalian expression systems, with Chinese hamster ovary (CHO) cells being the gold standard. CHO cells are ideal for the manufacturing of the IgG class of antibodies, but not for the production of complex antibodies like secretory IgAs (SIgAs) and IgMs, which remain unavailable for clinical use. In contrast, plant seeds and leaves hold the promise to produce SIgAs, IgMs and similar complex antibody formats to scalable amounts. Using transient transformation of Nicotiana benthamiana leaves, complex antibody formats can be produced up to milligram amounts in less than a month.

OBJECTIVE

Based on these merits, we propose a model for early-phase exploration and designing of innovative antibody formats for therapeutic application. Further in this essay, we elaborate how the model was followed during the selection of novel antibodies for seed-based production.

RESULT

This exploratory model led to the engineering of novel light-chain devoid porcinized-llama antibodies (VHH-Fc) of the IgG (VHH-IgG) and IgA (VHH-IgA) isotypes and also tetravalent dimeric and SIgAs.

CONCLUSION

The proposed strategy may lead to plant-based rapid engineering of innovative antibodies more apt and efficacious for therapy, and in the coarse also add to the understanding of their mode of action.

摘要

背景

用于人类临床应用的抗体主要在哺乳动物表达系统中产生,中国仓鼠卵巢(CHO)细胞是金标准。CHO细胞是生产IgG类抗体的理想选择,但不适合生产分泌型IgA(SIgA)和IgM等复杂抗体,这些抗体仍无法用于临床。相比之下,植物种子和叶片有望大量生产SIgA、IgM和类似的复杂抗体形式。利用本氏烟草叶片的瞬时转化,可在不到一个月的时间内生产出毫克量的复杂抗体形式。

目的

基于这些优点,我们提出了一种用于治疗应用的创新抗体形式的早期探索和设计模型。在本文中,我们进一步阐述了在选择基于种子生产的新型抗体时如何遵循该模型。

结果

该探索性模型导致了IgG(VHH-IgG)和IgA(VHH-IgA)同种型的新型无轻链猪源化骆驼抗体(VHH-Fc)以及四价二聚体和SIgA的工程化。

结论

所提出的策略可能导致基于植物的快速工程化创新抗体,这些抗体更适合且有效地用于治疗,并且在粗略层面上也有助于理解其作用模式。

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