封锁
免疫检查点
免疫系统
癌症研究
抗体
生物
免疫疗法
聚糖
细胞周期检查点
癌症免疫疗法
癌症
凝集素
T细胞
西格莱克
癌细胞
免疫学
体内
计算生物学
体外
细胞
细胞生物学
单克隆抗体
化学
PD-L1
调解人
嵌合抗原受体
小分子
作者
Jessica C. Stark,Melissa A. Gray,Itziar Ibarlucea-Benitez,Marta Lustig,Annalise Bond,B. Cho,Ishika Govil,T Luu,Megan Priestley,Tim S. Veth,Wesley J. Errington,Bence Bruncsics,Mikaela K. Ribi,L W Williams,Casim A. Sarkar,Simon Wisnovsky,Nicholas M. Riley,Meghan A. Morrissey,Thomas Valerius,Jeffrey V. Ravetch
标识
DOI:10.1038/s41587-025-02884-6
摘要
Despite the curative potential of checkpoint blockade immunotherapy, many patients remain unresponsive to existing treatments. Glyco-immune checkpoints, which involve interactions of cell-surface glycans with lectin, or glycan-binding, immunoreceptors, have emerged as prominent mechanisms of immune evasion and therapeutic resistance in cancer. Here, we describe antibody-lectin chimeras (AbLecs), a modular system for glyco-immune checkpoint blockade. AbLecs are bispecific antibody-like molecules comprising a cell-targeting antibody domain and a lectin 'decoy receptor' domain that directly binds glycans and blocks their ability to engage inhibitory lectin receptors. AbLecs potentiate cancer cell destruction by primary human immune cells in vitro and reduce tumour burden in a humanized, immunocompetent mouse model, outperforming most existing therapies and combinations tested. By targeting a distinct axis of immunological regulation, AbLecs synergize with blockade of established immune checkpoints. AbLecs can be readily designed to target numerous tumours and immune cell subsets as well as glyco-immune checkpoints, thus representing a potential modality for cancer immunotherapy.
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