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17 Apr 2024

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Academics

Scientists discovered first ligand of CD3 as target for cancer immunotherapy

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Recently, the research team led by Dr. Jie Xu from Institutes of Biomedical Sciences, Fudan University has shed light on CD3L1 (CD3 ligand 1), revealing it as a crucial mechanism in tumor immune evasion, particularly in patients who respond poorly to PD-1/PD-L1 inhibitory therapies. Results of the study have been published in Cell.

The expression of CD3L1 (or ITPRIPL1) exhibits several intriguing characteristics, including its mutual exclusivity with PD-L1 expression in most tumors, its prevalence in tumors resistant to PD-1/PD-L1 blockade, and enrichment in immune-privileged organs. These features suggest alternative immune evasion pathways and highlight the role of CD3L1 in maintaining immune privilege.

Furthermore, knockout studies in mice have demonstrated that CD3L1 plays a pivotal role in maintaining immune privilege, as its absence led to substantial autoimmune reactions in the testis. Additionally, a wide range of tumors express high levels of CD3L1, hindering T cell activity and enabling tumor immune evasion. The interaction of CD3L1 with CD3ε, a receptor, results in a sustained binding of Nck to the intracellular domain of CD3ε. This binding competitively inhibits the recruitment and phosphorylation of Zap70, effectively dampening T cell activation in its initial stages.

Previous research on TCR/CD3 receptor complex focused on TCR as the sole receptor for MHC ligands, while CD3 was thought to merely transduce TCR signals. This study reveals the existence of natural ligands for CD3, challenging the TCR-dominant model and introducing a bipolar mode where both TCR and CD3 can receive natural input signals. This groundbreaking discovery could significantly impact tumor immunotherapy drug development.

Image: The “jigsaw of target expression”, assembled by IHC staining of CD3L1 in various tumor tissue samples.

Dr. Jie Xu, a researcher of Institutes of Biomedical science, Fudan University, is the corresponding author of this paper. BioTroy Therapeutics participated in the collaborative research. This project was funded by key projects of the National Natural Science Foundation of China, national science and technology innovation leading talents research funds, Shanghai Science and Technology Innovation Action Plan, Fudan University Start-up Foundation. 

Currently the CD3L1 antibody is in phase I clinical trial, after obtaining the IND approval from FDA and China NMPA. Tumor patients interested in participating this clinical trial can contact BioTroy by e-mail (clin.oper@biotroy.cn).

Original article linkhttps://doi.org/10.1016/j.cell.2024.03.019

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Presented by Fudan University Media Center

Source: Institute of Biomedical Sciences, Fudan University

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