PO.IM01.13 · 免疫学

利用新型TCR模拟抗体偶联药物(TCRm-ADC)靶向细胞内KRAS G12D/HLA-A11 pMHC,在临床前模型中展现出强效抗肿瘤活性

Targeting intracellular KRAS G12D /HLA-A11 pMHC with a novel TCR-mimic antibody-drug conjugate (TCRm-ADC) demonstrates potent antitumor activity in preclinical models

海报缩略图:利用新型TCR模拟抗体偶联药物(TCRm-ADC)靶向细胞内KRAS G12D/HLA-A11 pMHC,在临床前模型中展现出强效抗肿瘤活性
编号 6929 展板 10 时间 4/22 09:00–12:00 区域 Section 6 主讲 Chia-Chun Chao
分会场 Antibody-Drug Conjugates 2
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作者与单位 Authors & Affiliations

Chia-Chun Chao1, Wei-Ze Hong1, Hsin-Yu Chang2, Jhen-Yu Chen3, Yi-Wen Jiang3, K.S. Clifford Chao3, Kevin Chih-Yang Huang3

1NDV Therapeutics Corp., Hsinchu, Taiwan,2National Yang Ming Chiao Tung University, Hsinchu, Taiwan,3China Medical University, Taichung, Taiwan

摘要 Abstract

中文摘要
靶向肿瘤相关抗原(TAA)的抗体偶联药物(ADC)常引起靶向、脱瘤的副作用。TCR模拟抗体(TCRm)模仿T细胞受体(TCR)与肽-MHC复合物(pMHC)相互作用的能力,为靶向此前不可成药的细胞内癌症抗原(如KRAS突变)提供了解决方案。在此,我们利用噬菌体展示、ELISA及基于细胞的实验,筛选并鉴定出一种对KRAS G12D/HLA-A*11 pMHC复合物具有高特异性和高亲和力的TCRm。我们进一步在体外和体内验证了该TCRm抗体的特异性和安全性。此外,靶向KRAS G12D/HLA-A*11 pMHC复合物的TCRm-ADC——NDV-ADC01-exatecan,在肺癌、胰腺癌和结直肠癌异种移植模型中于体外和体内介导了特异性抗肿瘤活性,且无明显毒性。另外,在人源化HLA-A*11/hB2M转基因模型中,NDV-ADC01-exatecan与低剂量放疗联合时,显著诱导了抗肿瘤免疫并重塑了肿瘤微环境。总之,这些筛选和工程改造过程为靶向不可成药的KRAS G12D突变癌症提供了一种新的治疗策略。
查看英文原文 English abstract
Antibody-drug conjugates (ADCs) targeting tumor-associated antigens (TAAs) frequently cause on-target, off-tumor side effects. TCR-mimic antibodies (TCRms) imitate the capacity of T cell receptors (TCRs) to interact with peptide-MHC complexes (pMHCs), offering a solution to target previously undruggable intracellular cancer antigens, such as KRAS mutations. Here, we screened and identified a TCRm with high specificity and affinity for the KRAS G12D /HLA-A*11 pMHC complex using phage display, ELISA, and cell-based assays. We further confirmed the specificity and safety of the TCRm antibody in vitro and in vivo . Furthermore, the TCRm-ADC, NDV-ADC01-exatecan, which targets the KRAS G12D /HLA-A*11 pMHC complex, mediated specific antitumor activity in vitro and in vivo without obvious toxicity in xenograft models of lung, pancreatic, and colorectal cancer. Additionally, NDV-ADC01-exatecan significantly elicited antitumor immunity and reshaped the tumor microenvironment when combined with low-dose radiotherapy in a humanized HLA-A*11/hB2M transgenic model. Together, these screening and engineering processes provide a novel therapeutic strategy to target undruggable KRAS G12D -mutated cancers.
利益披露 Disclosure
C. Chao, NDV Therapeutics Corp. Employment. W. Hong, NDV Therapeutics Corp. Employment. H. Chang, NDV Therapeutics Corp. Employment. J. Chen, None.. Y. Jiang, None.. K. Chao, None.. K. Huang, None.

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