Shen Ying, Wei Xiaoyue, Jin Shijie, Wu Yue, Zhao Wenbin, Xu Yingchun, Pan Liqiang, Zhou Zhan, Chen Shuqing
College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.
Huabo Biopharm Co., Ltd., Shanghai 201203, China.
Asian J Pharm Sci. 2020 Nov;15(6):777-785. doi: 10.1016/j.ajps.2020.01.002. Epub 2020 Mar 5.
Limited clinical application of antibody-drug conjugates (ADCs) targeting tumor associated antigens (TAAs) is usually caused by on-target off-tumor side effect. Tumor-specific mutant antigens (TSMAs) only expressed in tumor cells which are ideal targets for ADCs. In addition, intracellular somatic mutant proteins can be presented on the cell surface by human leukocyte antigen class I (HLA I)molecules forming tumor-specific peptide/HLA I complexes. KRAS G12V mutation frequently occurred in varied cancer and was verified as a promising target for cancer therapy. In this study, we generated two TCR-mimic antibody-drug conjugates (TCRm-ADCs), 2E8-MMAE and 2A5-MMAE, targeting KRAS G12V/HLA-A*0201 complex, which mediated specific antitumor activity and without obvious toxicity. Our findings are the first time validate the strategy of TCRm-ADCs targeting intracellular TSMAs, which improves the safety of antibody-based drugs and provides novel strategy for precision medicine in cancer therapy.
靶向肿瘤相关抗原(TAA)的抗体药物偶联物(ADC)临床应用受限通常是由靶上非肿瘤副作用引起的。肿瘤特异性突变抗原(TSMA)仅在肿瘤细胞中表达,是ADC的理想靶点。此外,细胞内体细胞突变蛋白可通过人类白细胞抗原I类(HLA I)分子呈递到细胞表面,形成肿瘤特异性肽/HLA I复合物。KRAS G12V突变在多种癌症中频繁发生,并被证实是癌症治疗的一个有前景的靶点。在本研究中,我们制备了两种靶向KRAS G12V/HLA-A*0201复合物的T细胞受体模拟抗体药物偶联物(TCRm-ADC),即2E8-MMAE和2A5-MMAE,它们介导了特异性抗肿瘤活性且无明显毒性。我们的研究结果首次验证了TCRm-ADC靶向细胞内TSMA的策略,该策略提高了基于抗体药物的安全性,并为癌症治疗中的精准医学提供了新策略。