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体外经 LacO/LacI 调控网络加速的抗体发现。

Antibody discovery ex vivo accelerated by the LacO/LacI regulatory network.

机构信息

Department of Immunology, University of Washington School of Medicine, Seattle, Washington, USA.

出版信息

PLoS One. 2012;7(4):e36032. doi: 10.1371/journal.pone.0036032. Epub 2012 Apr 27.

Abstract

Monoclonal antibodies (mAbs) can be potent and highly specific therapeutics, diagnostics and research reagents. Nonetheless, mAb discovery using current in vivo or in vitro approaches can be costly and time-consuming, with no guarantee of success. We have established a platform for rapid discovery and optimization of mAbs ex vivo. This DTLacO platform derives from a chicken B cell line that has been engineered to enable rapid selection and seamless maturation of high affinity mAbs. We have validated the DTLacO platform by generation of high affinity and specific mAbs to five cell surface targets, the receptor tyrosine kinases VEGFR2 and TIE2, the glycoprotein TROP2, the small TNF receptor family member FN14, and the G protein-coupled receptor FZD10. mAb discovery is rapid and humanization is straightforward, establishing the utility of the DTLacO platform for identification of mAbs for therapeutic and other applications.

摘要

单克隆抗体(mAbs)可以是强效且高度特异的治疗药物、诊断试剂和研究试剂。尽管如此,使用当前的体内或体外方法进行 mAb 发现可能成本高昂且耗时,并且不能保证成功。我们已经建立了一个用于快速发现和优化体外 mAbs 的平台。这个 DTLacO 平台源自经过工程改造的鸡 B 细胞系,可实现高亲和力 mAbs 的快速选择和无缝成熟。我们通过生成针对五个细胞表面靶标的高亲和力和特异性 mAbs 验证了 DTLacO 平台的有效性,这些靶标包括受体酪氨酸激酶 VEGFR2 和 TIE2、糖蛋白 TROP2、小 TNF 受体家族成员 FN14 和 G 蛋白偶联受体 FZD10。mAb 的发现速度很快,并且易于人源化,这证明了 DTLacO 平台对于鉴定治疗和其他应用的 mAbs 的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc7b/3338700/45f282d03728/pone.0036032.g001.jpg

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