Agnostic B cell selection approach identifies antibodies against K. pneumoniae that synergistically drive complement activation.

Abstract

Abstract Antibody-dependent complement activation plays a key role in the natural human immune response to infections. Currently, the understanding of which antibody-antigen combinations drive a potent complement response on bacteria is limited. Here, we develop an antigen-agnostic approach to stain and single-cell sort human IgG memory B cells recognizing intact bacterial cells, keeping surface antigens in their natural context. With this method we successfully identified 29 unique antibodies against K. pneumoniae, a dominant cause of hospital-acquired infections with increasing antibiotic resistance. Combining genetic tools and functional analyses, we reveal that the capacity of antibodies to activate complement on K. pneumoniae critically depends on their antigenic target. Furthermore, we find that certain antibody combinations can act synergistically to activate complement on K. pneumoniae. Understanding the molecular basis of effective complement activation by monoclonals or combining antibodies to mimic a polyclonal response could accelerate the development of antibody-based therapies against problematic infections.