Conditional activation of an anti-IgM antibody-drug conjugate for precise B cell lymphoma targeting

被引:6
|
作者
Schoenfeld, Katrin [1 ]
Harwardt, Julia [1 ]
Habermann, Jan [1 ]
Elter, Adrian [1 ]
Kolmar, Harald [1 ,2 ]
机构
[1] Tech Univ Darmstadt, Inst Organ Chem & Biochem, Darmstadt, Germany
[2] Tech Univ Darmstadt, Ctr Synthet Biol, Darmstadt, Germany
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
B cell receptor; antibody-drug conjugate; masked antibody; conditional activated antibody; MMP-9; matriptase; B cell lymphoma; BISPECIFIC ANTIBODY; PHASE-I; V-H; SURFACE; GENERATION; PHOSPHORYLATION; THERAPEUTICS; RESISTANCE; EXPRESSION; LIBRARIES;
D O I
10.3389/fimmu.2023.1258700
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页数:14
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