Institute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, Darmstadt, Germany.
Centre for Synthetic Biology, Technical University of Darmstadt, Darmstadt, Germany.
Front Immunol. 2023 Sep 28;14:1258700. doi: 10.3389/fimmu.2023.1258700. eCollection 2023.
Cancerous B cells are almost indistinguishable from their non-malignant counterparts regarding their surface antigen expression. Accordingly, the challenge to be faced consists in elimination of the malignant B cell population while maintaining a functional adaptive immune system. Here, we present an IgM-specific antibody-drug conjugate masked by fusion of the epitope-bearing IgM constant domain. Antibody masking impaired interaction with soluble pentameric as well as cell surface-expressed IgM molecules rendering the antibody cytotoxically inactive. Binding capacity of the anti-IgM antibody drug conjugate was restored upon conditional protease-mediated demasking which consequently enabled target-dependent antibody internalization and subsequent induction of apoptosis in malignant B cells. This easily adaptable approach potentially provides a novel mechanism of clonal B cell lymphoma eradication to the arsenal available for non-Hodgkin's lymphoma treatment.
在表面抗原表达方面,癌细胞 B 与非恶性细胞 B 几乎无法区分。因此,面临的挑战是在保留功能性适应性免疫系统的同时消除恶性 B 细胞群体。在这里,我们展示了一种 IgM 特异性抗体 - 药物偶联物,通过融合带有表位的 IgM 恒定结构域进行掩蔽。抗体掩蔽会削弱与可溶性五聚体以及细胞表面表达的 IgM 分子的相互作用,从而使抗体细胞毒性失活。条件性蛋白酶介导的去掩蔽恢复了抗 IgM 抗体药物偶联物的结合能力,从而能够使抗体依赖于靶标内化,并随后诱导恶性 B 细胞凋亡。这种易于适应的方法可能为非霍奇金淋巴瘤治疗提供了一种新的克隆性 B 细胞淋巴瘤消除机制。