Abstract

Harnessing complement-mediated cytotoxicity by therapeutic antibodies has been limited because of dependency on size and density of antigen, structural constraints resulting from orientation of antibody binding, and blockade of complement activation by inhibitors expressed on target cells. We developed a modular bispecific antibody platform that directs the complement-initiating protein C1q to target cells, increases local complement deposition and induces cytotoxicity against target antigens with a wide-range of expression. The broad utility of this approach to eliminate both prokaryotic and eukaryotic cells was demonstrated by pairing a unique C1q-recruiting arm with multiple targeting arms specific for Staphylococcus aureus, Pseudomonas aeruginosa, B-cells and T-cells, indicating applicability for diverse indications ranging from infectious diseases to cancer. Generation of C1q humanized mice allowed for demonstration of the efficacy of this approach to clear disease-inducing cells in vivo. In summary, we present a novel, broadly applicable, and versatile therapeutic modality for targeted cell depletion.

Highlights

  • Therapeutics that direct powerful effector functions of the immune system towards target cells hold great promise in settings of therapeutic resistance of infectious diseases and cancer

  • We demonstrate that S. aureus is sensitive to the bactericidal activity of serum, and this activity is enhanced by the C1q-recruiting bispecific antibodies (bsAbs) in vitro and in vivo

  • These results demonstrate that anti-iron-regulated surface determinant protein B (IsdB) x anti-C1q enhances killing of S. aureus and supports a C1q-recruiting bsAb approach to augment complement activity

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Summary

Introduction

Therapeutics that direct powerful effector functions of the immune system towards target cells hold great promise in settings of therapeutic resistance of infectious diseases and cancer. We measured C1q deposition on the surface of S. aureus Newman (a methicillin-sensitive strain, MSSA) resulting www.nature.com/scientificreports from binding of anti-IsdB x anti-C1q bsAb, the bivalent IsdB antibody or an isotype control antibody.

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