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利用位点特异性生物偶联拓宽抗体药物偶联物的治疗窗口:以靶向CD79b的抗体药物偶联物中含MMAE的肽接头为例

Broadening the Therapeutic Window of ADCs Using Site-Specific Bioconjugation Showcased by an MMAE-Containing Peptide Linker in a CD79b-Targeting ADC.

作者信息

Probst Philipp, Attinger-Toller Isabella, Bertrand Romain, Stark Ramona, Santimaria Roger, Schlereth Bernd, Grabulovski Dragan, Spycher Philipp René

机构信息

Araris Biotech AG, Au ZH, Switzerland.

出版信息

Mol Cancer Ther. 2025 Jun 4;24(6):803-815. doi: 10.1158/1535-7163.MCT-24-0983.

Abstract

The limitations of first-generation antibody-drug conjugate (ADC) technologies include suboptimal stability and efficacy, poor safety profiles, and challenging manufacturing processes. In this study, we describe an anti-CD79b-monomethyl auristatin E (MMAE) ADC generated using a novel peptide-based linker technology that allows for site-specific linker-payload conjugation to native antibodies in only one step. The ADC comprises native polatuzumab as the targeting antibody and a linker-payload consisting of a RKAA-peptide linker and MMAE. We compared our anti-CD79b-RKAA-MMAE ADC with polatuzumab vedotin (PV), the FDA-approved ADC for diffuse large B-cell lymphoma. In the clinic, PV shows significant instability in circulation, leading to strong and dose-limiting side effects, including neutropenia and peripheral neuropathy. The anti-CD79b-RKAA-MMAE ADC showed optimal biophysical properties with a well-defined drug-to-antibody ratio of 2. It demonstrated potent cytotoxicity in multiple cancer cell lines and was very stable in mouse, cynomolgus monkey, and human sera. The anti-CD79b-RKAA-MMAE conjugate showed equal antitumor efficacy at half the payload dose compared with PV in different xenograft models. At equal MMAE concentrations, greater tumor growth inhibition and a considerably longer duration of response were observed. Ultimately, the highest nonseverely toxic dose of 30 mg/kg was determined in a 4-week repeat-dose toxicology study in rats, which is a 3-fold higher ADC dose than reported for PV. In summary, the data show that our novel site-specific bioconjugation technology enabled the generation of an anti-CD79b-RKAA-MMAE ADC with highly favorable biophysical properties and a greatly improved therapeutic index by a factor of 4 to 6 compared with PV. The ADC may therefore represent a safe and efficacious alternative for patients with diffuse large B-cell lymphoma.

摘要

第一代抗体药物偶联物(ADC)技术的局限性包括稳定性和疗效欠佳、安全性较差以及生产工艺具有挑战性。在本研究中,我们描述了一种使用基于新型肽的连接子技术生成的抗CD79b-单甲基奥瑞他汀E(MMAE)ADC,该技术仅需一步即可实现连接子-载荷与天然抗体的位点特异性偶联。该ADC包含天然泊洛妥珠单抗作为靶向抗体以及由RKAA肽连接子和MMAE组成的连接子-载荷。我们将我们的抗CD79b-RKAA-MMAE ADC与泊洛妥珠单抗(PV)进行了比较,PV是FDA批准用于弥漫性大B细胞淋巴瘤的ADC。在临床上,PV在循环中表现出显著的不稳定性,导致强烈的剂量限制性副作用,包括中性粒细胞减少和周围神经病变。抗CD79b-RKAA-MMAE ADC显示出最佳的生物物理性质,药物与抗体的比例明确为2。它在多种癌细胞系中表现出强大的细胞毒性,并且在小鼠、食蟹猴和人血清中非常稳定。在不同的异种移植模型中,抗CD79b-RKAA-MMAE偶联物在载荷剂量减半时显示出与PV相当的抗肿瘤疗效。在MMAE浓度相等的情况下,观察到更大的肿瘤生长抑制和显著更长的反应持续时间。最终,在大鼠的4周重复剂量毒理学研究中确定了最高非严重毒性剂量为30 mg/kg,这是报道的PV的ADC剂量的3倍。总之,数据表明我们的新型位点特异性生物偶联技术能够生成具有高度有利生物物理性质的抗CD79b-RKAA-MMAE ADC,并且与PV相比,治疗指数提高了4至6倍。因此,该ADC可能是弥漫性大B细胞淋巴瘤患者的一种安全有效的替代方案。

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