Fig. 1.
Fig. 1. Schematic representation of different types of cytotoxicity assays employed in this study. (A) Shows conventional ADCC against haptenized SK-BR–3 breast cancer cells via NIP-directed antibodies. FcR blocking antibodies served to identify trigger molecules involved in IgA-mediated ADCC. In (B), a novel reverse ADCC assay is shown using hybridoma target cells, which were selected for high membrane expression of their surface Ig directed to mouse κ light chains. In the presence of Fc receptor antibodies, these hybridoma cells are sensitized for reverse ADCC. (C) Shows recruitment of Fc receptor positive effector cells via BsAbs.

Schematic representation of different types of cytotoxicity assays employed in this study. (A) Shows conventional ADCC against haptenized SK-BR–3 breast cancer cells via NIP-directed antibodies. FcR blocking antibodies served to identify trigger molecules involved in IgA-mediated ADCC. In (B), a novel reverse ADCC assay is shown using hybridoma target cells, which were selected for high membrane expression of their surface Ig directed to mouse κ light chains. In the presence of Fc receptor antibodies, these hybridoma cells are sensitized for reverse ADCC. (C) Shows recruitment of Fc receptor positive effector cells via BsAbs.

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