TUB-010是一种基于tub标签技术的新型抗cd30抗体-药物偶联物,通过降低毒性同时保持高效率,拓宽了治疗窗口。

IF 5.5 2区 医学 Q1 ONCOLOGY
Marcus Gerlach, Saskia Schmitt, Philipp Cyprys, Marc-André Kasper, Isabelle Mai, Magdalena Klanova, Andreas Maiser, Heinrich Leonhardt, Christian P R Hackenberger, Günter R Fingerle-Rowson, Annette M Vogl, Dominik Schumacher, Jonas Helma
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引用次数: 0

摘要

TUB-010是新一代抗体-药物偶联物(ADC),靶向多种造血恶性肿瘤(如霍奇金淋巴瘤)中表达的CD30。在复发和难治性cd30阳性癌症患者的治疗选择中,brentuximab vedotin (Adcetris)是一种mmae递送抗cd30 ADC,平均药抗体比(DAR)为4。Adcetris表现出高响应率,但代价是显著的毒性,可能是由有效载荷MMAE和马来酰亚胺偶联化学的不稳定性驱动的。TUB-010使用与Adcetris相同的抗体和有效载荷,但基于Tub-tag偶联策略,通过化学酶偶联将MMAE稳定地附着在轻链上的亲水Tub-tag肽上。这项新技术能够生成具有独特生物物理特性的同质和位点特异性DAR 2 ADC。TUB-010表现出与Adcetris相似的结合和溶酶体释放特性,当归一化到MMAE浓度时,对cd30阳性细胞系的体外细胞毒性相当。重要的是,与Adcetris相比,TUB-010表现出更高的稳定性,在循环中可以忽略不计过早脱偶和减少聚集,并且对靶阴性细胞具有更低的非特异性细胞毒性。因此,与Adcetris相比,在体内以相同的MMAE浓度给药时,TUB-010可诱导更好的肿瘤控制,并且在啮齿动物和非人灵长类动物中毒性更低,耐受性更高。综上所述,TUB-010是一种新型的、潜在的同类最佳抗cd30 ADC,具有改进的生物物理特性,旨在提供比使用tub标签技术的Adcetris更高精度的MMAE和更宽的治疗窗口。因此,TUB-010可能会增加抗cd30 ADC治疗的临床获益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TUB-010, a novel anti-CD30 antibody-drug conjugate based on Tub-tag technology, widens the therapeutic window by reducing toxicity while maintaining high efficacy.

TUB-010 is a next-generation antibody-drug conjugate (ADC) targeting CD30 expressed on various hematopoietic malignancies such as Hodgkin lymphoma. Among the therapeutic options for patients with relapsed and refractory CD30-positive cancers is brentuximab vedotin (Adcetris), an MMAE-delivering anti-CD30 ADC with a mean drug-to antibody ratio (DAR) of 4. Adcetris exhibits a high response rate at the cost of significant toxicities, likely driven by the payload MMAE and instability of the maleimide conjugation chemistry. TUB-010 uses the same antibody and payload as Adcetris, but is based on the Tub-tag conjugation strategy, which stably attaches MMAE to the hydrophilic Tub-tag peptides on the light chains via chemoenzymatic conjugation. This new technology enables the generation of a homogenous and site-specific DAR 2 ADC with unique biophysical properties. TUB-010 demonstrates similar binding and lysosomal release characteristics as Adcetris, which translates into comparable in vitro cytotoxicity on CD30-positive cell lines when normalized to the MMAE concentration. Importantly, TUB-010 exhibits higher stability with neglectable premature deconjugation in circulation and reduced aggregation as well as lower non-specific cytotoxicity on target-negative cells compared to Adcetris. As a consequence, TUB-010 induces superior tumor control compared to Adcetris when dosed at equal MMAE concentrations in vivo and also lower toxicity and higher tolerability in rodents and non-human primates. Taken together, TUB-010 is a novel, potential best-in-class anti-CD30 ADC with improved biophysical properties designed to deliver MMAE with higher precision and a wider therapeutic window than Adcetris using Tub-tag technology. Therefore, TUB-010 may increase the clinical benefit of anti-CD30 ADC therapies.

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来源期刊
CiteScore
11.20
自引率
1.80%
发文量
331
审稿时长
3 months
期刊介绍: Molecular Cancer Therapeutics will focus on basic research that has implications for cancer therapeutics in the following areas: Experimental Cancer Therapeutics, Identification of Molecular Targets, Targets for Chemoprevention, New Models, Cancer Chemistry and Drug Discovery, Molecular and Cellular Pharmacology, Molecular Classification of Tumors, and Bioinformatics and Computational Molecular Biology. The journal provides a publication forum for these emerging disciplines that is focused specifically on cancer research. Papers are stringently reviewed and only those that report results of novel, timely, and significant research and meet high standards of scientific merit will be accepted for publication.
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