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Fc-engineered monoclonal antibodies to reduce off-target liver uptake
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Fc-engineered monoclonal antibodies to reduce off-target liver uptake
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Fc-engineered monoclonal antibodies to reduce off-target liver uptake
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Fc-engineered monoclonal antibodies to reduce off-target liver uptake
Fc-engineered monoclonal antibodies to reduce off-target liver uptake
Journal Article

Fc-engineered monoclonal antibodies to reduce off-target liver uptake

2023
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Overview
BackgroundRadiolabeled-antibodies usually display non-specific liver accumulation that may impair image analysis and antibody biodistribution. Here, we investigated whether Fc silencing influenced antibody biodistribution. We compared recombinant 89Zr-labeled antibodies (human IgG1 against different targets) with wild-type Fc and with mutated Fc (LALAPG triple mutation to prevent binding to Fc gamma receptors; FcγR). After antibody injection in mice harboring xenografts of different tumor cell lines or of immortalized human myoblasts, we analyzed antibody biodistribution by PET-CT and conventional biodistribution analysis.ResultsAccumulation in liver was strongly reduced and tumor-specific targeting was increased for the antibodies with mutated Fc compared with wild-type Fc.ConclusionAntibodies with reduced binding to FcγR display lower liver accumulation and better tumor-to-liver ratios. These findings need to be taken into account to improve antibody-based theragnostic approaches.

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