Chimeric antigen receptor (CAR) T cell therapy has achieved remarkable success in hematological malignancies. However, its efficacy in hepatocellular carcinoma (HCC) remains limited. One major challenge is the lack of reliable tumor antigens for CAR T cell recognition. CD44E, a unique alternative splicing (AS) variant of CD44 transmembrane protein that is highly expressed in HCC tumors compared to adjacent non-tumoral liver tissues, holds promise as a potential therapeutic target. Here, we successfully developed a CD44E-specific monoclonal antibody derived from the S431 hybridoma clone. Using this antibody, we confirmed CD44E protein expression in patient-derived HCC cell lines, organoids, and primary tumor tissues. A second-generation CAR was designed by incorporating the single-chain variable fragment (scFv) of the S431 antibody. These anti-CD44E CAR T cells exhibited specific cytotoxicity against CD44-positive HCC cells in both in vitro and in vivo models and importantly, did not induce detectable toxicity in vital organs in animal models. Our findings suggested that CD44E-targeting CAR T cell therapy might represent a promising therapeutic approach for HCC treatment.
Chimeric antigen receptor T cell targeting CD44E variant in HCC holds therapeutic potential.
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作者:Liao Rui, Chan Cecilia Ka Wing, Cui Yuanbin, Li Shanglin, Ma Ruiying, Peng Dongdong, Mei Piaorong, Xu Mingjing, Li Peng, Wong Nathalie
| 期刊: | Molecular Therapy Oncology | 影响因子: | 5.300 |
| 时间: | 2026 | 起止号: | 2026 Mar 18; 34(2):201181 |
| doi: | 10.1016/j.omton.2026.201181 | ||
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