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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:
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.
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页数:14
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