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Human germline-like monoclonal antibody against 5T4 enables potent ADC and CAR-T therapies for solid tumors

Yi-qing Jiang1, Xiao-jie Ma1, Yin-man Wang2,3, Yi Feng1, Yu Kong1,4, Ai-ling Huang1,4, Zi-xuan Jin1, Tian-lei Ying1,4, Yan-ling Wu1,4
1 Key Laboratory of Medical Molecular Virology (MOE/NHC/CAMS) and Shanghai Institute of Infectious Disease and Biosecurity, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China
2 Department of Cardiology, Zhongshan Hospital, Fudan University (Xiamen Branch), Xiamen 361015, China
3 Department of Cardiology, Zhongshan Hospital, Fudan University, Shanghai Institute of Cardiovascular Diseases, State Key Laboratory of Cardiovascular Diseases, National Clinical Research Center for Interventional Medicine, Shanghai 200032, China
4 Shanghai Engineering Research Center for Synthetic Immunology, Shanghai 200032, China
Correspondence to: Yin-man Wang: wang.yinman@zs-hospital.sh.cn, Tian-lei Ying: tlying@fudan.edu.cn, Yan-ling Wu: yanlingwu@fudan.edu.cn,
DOI: 10.1038/s41401-025-01731-3
Received: 31 May 2025
Accepted: 4 December 2025
Advance online: 27 January 2026

Abstract

5T4 is an oncofetal antigen overexpressed in a wide range of solid tumors with minimal presence in normal adult tissues, highlighting its promise as a therapeutic target. In this study, we identified germline-like human monoclonal antibodies targeting human 5T4 with high affinity, among which antibody m603 exhibits superior cell binding activity to various cancer cells including breast, pancreatic, ovarian, lung and liver cancer cell lines. Subsequently, we constructed antibody-drug conjugates (ADCs) and chimeric antigen receptor (CAR)-T cell based on m603. By conjugating the antibody with cytotoxic payload DM4 or MMAE, the resulting ADCs demonstrated potent and antigen-dependent cell killing activity in vitro. The ADC conjugated with MMAE payload elicited durable tumor suppression in pancreatic cancer xenograft models. Furthermore, third-generation CAR-T cells derived from m603 (603z-CAR-T), incorporating 4-1BB and CD28 costimulatory domains, effectively induced IFN-γ and IL-2 secretion and remarkable tumor eradication. The germline-like antibody as a versatile platform for 5T4-targeted therapies offers promising immunotherapies for treating solid tumors.
Keywords: solid tumors; 5T4; germline-like monoclonal antibody; antibody-drug conjugate; chimeric antigen receptor T cell; pancreatic cancer

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