PO.ET02.04 · 实验与分子治疗

YB-811:一种靶向肿瘤选择性人神经元五聚体蛋白受体的新型抗体药物偶联物,在实验性肿瘤模型中显示出显著疗效

YB-811, a novel antibody drug conjugate targeting the tumor-selective human neuronal pentraxin receptor shows pronounced efficacy in experimental tumor models

编号 5633 展板 3 时间 4/21 02:00–05:00 区域 Section 10 主讲 Peter Schiemann, PhD
分会场 Antibody-Drug Conjugates and Linker Engineering 4
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作者与单位 Authors & Affiliations

Peter Schiemann1, Michel Janicot1, Gunther Wennemuth2, Mykola Lyndin2

1Ymmunobio AG, Riehen, Switzerland,2University Hospital Essen, Essen, Germany

摘要 Abstract

中文摘要
人神经元五聚体蛋白受体(NPTXR)基因编码一种II型跨膜蛋白,其作为跨突触组织者发挥功能,并将神经元五聚体蛋白复合物锚定于海马和大脑皮层一部分神经元细胞的质膜上。除其在脑内的突触功能外,NPTXR不存在于其他器官,因此不具有任何生理作用;因此NPTXR−/−小鼠在生殖、发育、代谢或运动功能方面未显示异常。近期使用一种以高亲和力靶向NPTXR的全人源化单克隆抗体(YB-800)进行的免疫组织化学研究揭示,膜相关NPTXR蛋白在多种多样的实体瘤中表达(但不在邻近健康组织和健康组织样本中表达),具有高流行率(高达98%)和H评分(高达300);例如在膀胱、宫颈、非TNBC、NSCLC和胰腺肿瘤样本中。这些结果有力地支持了设计基于YB-800的抗体药物偶联物(ADC)作为肿瘤学中安全治疗干预新选择的理论依据。设计了一种新型ADC(YB-811),将YB-800与4个单甲基auristatin F分子(通过不可裂解连接子)和4个exatecan分子(通过可裂解连接子)连接。YB-811在多个实验性肿瘤模型中通过基于细胞的测定和体内肿瘤研究进行了评估。结果清楚地表明对肿瘤细胞增殖和存活具有浓度和时间依赖性效应,以及在已建立的荷瘤裸鼠中具有显著的抗肿瘤活性——肿瘤生长抑制/消退。综上所述,这些结果有力地支持进一步探索YB-811潜在的治疗益处。
查看英文原文 English abstract
The human neuronal pentraxin receptor (NPTXR) gene encodes a type II transmembrane protein that functions as a trans-synaptic organizer and anchors neuronal pentraxin complexes to plasma membranes in a subset of neuronal cells of the hippocampus and cerebral cortex. Beside its synaptic functions in the brain, NPTXR is not present in other organs and therefore does not have any physiological role; hence NPTXR −/− mice showed no abnormalities in reproduction, development, metabolism, or motor function. Recent immunohistochemistry studies performed with a fully humanized monoclonal antibody (YB-800) targeting NPTXR with high affinity have revealed expression of membrane-associated NPTXR protein in a wide variety of solid tumors (but not in adjacent healthy tissues and healthy tissue samples) with a high prevalence (up to 98%) and H-scores (up to 300); e.g., in bladder, cervix, non-TNBC, NSCLC, and pancreas tumor samples. These results strongly support the rationale for the design of a YB-800-based antibody drug conjugate (ADC) as novel option for safe therapeutic intervention in Oncology. A novel ADC (YB-811) was engineered with YB-800 linked to 4 monomethylauristatin F molecules ( via non-cleavable linkers), and 4 exatecan molecules ( via cleavable linkers). YB-811 was evaluated in multiple experimental tumor models in both cell-based assays and in vivo tumor studies. Results clearly indicate concentration- and time-dependent effect on tumor cell proliferation and survival, as well as pronounced anti-tumor activity - tumor growth inhibition/regression - in established tumor-bearing athymic mice. Taken together, these results strongly support further exploration of the potential therapeutic benefit of YB-811.
利益披露 Disclosure
P. Schiemann, None.. M. Janicot, None.. G. Wennemuth, None.. M. Lyndin, None.

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