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Cancer Biol Ther. 2017 May 4;18(5):347-357. doi: 10.1080/15384047.2017.1312232. Epub 2017 Apr 10.
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本文引用的文献

1
Engineering humanized antibody framework sequences for optimal site-specific conjugation of cytotoxins.设计人源化抗体框架序列以实现细胞毒素的最佳位点特异性偶联。
MAbs. 2017 Aug/Sep;9(6):907-915. doi: 10.1080/19420862.2017.1330734. Epub 2017 May 25.
2
Humanization of rabbit monoclonal antibodies via grafting combined Kabat/IMGT/Paratome complementarity-determining regions: Rationale and examples.通过移植组合的Kabat/IMGT/Paratome互补决定区实现兔单克隆抗体人源化:原理与实例
MAbs. 2017 Apr;9(3):419-429. doi: 10.1080/19420862.2017.1289302. Epub 2017 Feb 6.
3
Brentuximab vedotin for treatment of non-Hodgkin lymphomas: A systematic review.用于治疗非霍奇金淋巴瘤的维布妥昔单抗:一项系统评价。
Crit Rev Oncol Hematol. 2017 Jan;109:42-50. doi: 10.1016/j.critrevonc.2016.11.009. Epub 2016 Nov 21.
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Mesothelin Immunotherapy for Cancer: Ready for Prime Time?间皮素免疫疗法治疗癌症:准备好进入黄金时代了吗?
J Clin Oncol. 2016 Dec;34(34):4171-4179. doi: 10.1200/JCO.2016.68.3672. Epub 2016 Oct 31.
5
Antibody-drug conjugates: recent advances in conjugation and linker chemistries.抗体偶联药物:偶联和连接子化学的最新进展。
Protein Cell. 2018 Jan;9(1):33-46. doi: 10.1007/s13238-016-0323-0. Epub 2016 Oct 14.
6
Rapid high-throughput cloning and stable expression of antibodies in HEK293 cells.抗体在HEK293细胞中的快速高通量克隆与稳定表达。
J Immunol Methods. 2016 Dec;439:50-58. doi: 10.1016/j.jim.2016.09.007. Epub 2016 Sep 24.
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Antibody drug conjugates.抗体药物偶联物
Biotechnol Lett. 2016 Oct;38(10):1655-64. doi: 10.1007/s10529-016-2160-x. Epub 2016 Jun 22.
8
One-Step Conjugation Method for Site-Specific Antibody-Drug Conjugates through Reactive Cysteine-Engineered Antibodies.通过反应性半胱氨酸工程化抗体实现位点特异性抗体-药物偶联物的一步偶联方法。
Bioconjug Chem. 2016 May 18;27(5):1324-31. doi: 10.1021/acs.bioconjchem.6b00133. Epub 2016 Apr 28.
9
Cysteinylation of a monoclonal antibody leads to its inactivation.单克隆抗体的半胱氨酸化会导致其失活。
MAbs. 2016 May-Jun;8(4):718-25. doi: 10.1080/19420862.2016.1160179. Epub 2016 Apr 6.
10
New developments for antibody-drug conjugate-based therapeutic approaches.抗体药物偶联物治疗方法的新进展。
Curr Opin Immunol. 2016 Jun;40:14-23. doi: 10.1016/j.coi.2016.02.008. Epub 2016 Mar 7.

通过利用穴兔轻链框架中的天然半胱氨酸的残基特异性偶联技术(RESPECT)生成治疗性免疫偶联物。

Generation of therapeutic immunoconjugates via Residue-Specific Conjugation Technology (RESPECT) utilizing a native cysteine in the light chain framework of Oryctolagus cuniculus.

作者信息

Albone Earl F, Spidel Jared L, Cheng Xin, Park Young Chul, Jacob Sara, Milinichik Andrew Z, Vaessen Ben, Butler Janet, Kline J Bradford, Grasso Luigi

机构信息

a Morphotek Inc. , Exton , PA , USA.

出版信息

Cancer Biol Ther. 2017 May 4;18(5):347-357. doi: 10.1080/15384047.2017.1312232. Epub 2017 Apr 10.

DOI:10.1080/15384047.2017.1312232
PMID:28394698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5499757/
Abstract

The conjugation of toxins, dyes, peptides, or proteins to monoclonal antibodies is often performed via free thiol groups generated by either partial reduction methods or engineering free cysteine residues into the antibody sequence. Antibodies from the rabbit Oryctolagus cuniculus have an additional intrachain disulfide bond, whereby the light chain variable kappa domain is bridged to the constant kappa region between cysteine residues at positions 80 and 171, respectively. Chimerization of rabbit antibodies with human constant domains allows for the generation of a free thiol group at the light chain position 80 (C80) that can be used for site-specific conjugation. An efficient process for the purification and simultaneous removal of cysteinylation at the C80 site was developed. The unpaired C80 was shown to be efficiently conjugated using several different maleimido-based ligands. REsidue SPEcific Conjugation Technology (RESPECT) antibody-drug conjugates prepared using rabbit-human chimeric anti-human mesothelin rabbit antibodies and maleimido-PEG-auristatin conjugated to C80 were shown to be highly potent and specific in vitro and effective in vivo in reduction of tumor growth in a highly aggressive mesothelin-expressing xenograft tumor model.

摘要

毒素、染料、肽或蛋白质与单克隆抗体的缀合通常通过部分还原方法产生的游离硫醇基团或在抗体序列中引入游离半胱氨酸残基来进行。来自兔穴兔的抗体具有一个额外的链内二硫键,由此轻链可变κ结构域分别在第80位和第171位的半胱氨酸残基之间桥接到恒定κ区域。将兔抗体与人恒定结构域进行嵌合可在轻链第80位(C80)产生一个可用于位点特异性缀合的游离硫醇基团。开发了一种高效的纯化方法,可同时去除C80位点的半胱氨酸化修饰。使用几种不同的基于马来酰亚胺的配体已证明未配对的C80能够有效地进行缀合。使用兔-人嵌合抗人间皮素兔抗体和与C80缀合的马来酰亚胺-聚乙二醇-奥瑞他汀制备的残基特异性缀合技术(RESPECT)抗体-药物缀合物在体外表现出高效力和特异性,并且在高度侵袭性的表达间皮素的异种移植肿瘤模型中,在体内对肿瘤生长的抑制有效。