The classical pathway is the dominant complement pathway required for innate immunity toStreptococcus pneumoniaeinfection in mice

• DOI: 10.1073/pnas.012669199
• Publication Date: 2002-12-23T18:14:48Z
• Authors: Jeremy S. Brown; Tracy Hussell; Sarah M. Gilliland; David W. Holden; James C. Paton; Michael R. Ehrens...; Mark J. Walport; Marina Botto
• Keywords: Alternative; 570; Complement C1q; Complement Pathway, Alternative; Immunity; Complement C3; Inbred C57BL; Immunity, Innate; Pneumococcal Infections; Classical; 3. Good health; Mice, Inbred C57BL; Mice; 03 medical and health sciences; Streptococcus pneumoniae; 0302 clinical medicine; Immunoglobulin M; Complement Pathway; Immunoglobulin G; Innate; Animals; Complement Pathway, Classical

The complement system is an important component of the innate immune response to bacterial pathogens, includingStreptococcus pneumoniae. The classical complement pathway is activated by antibody–antigen complexes on the bacterial surface and has been considered predominately to be an effector of the adaptive immune response, whereas the alternative and mannose-binding lectin pathways are activated directly by bacterial cell surface components and are considered effectors of the innate immune response. Recently, a role has been suggested for the classical pathway during innate immunity that is activated by natural IgM or components of the acute-phase response bound to bacterial pathogens. However, the functional importance of the classical pathway for innate immunity toS. pneumoniaeand other bacterial pathogens, and its relative contribution compared with the alternative and mannose-binding lectin pathways has not been defined. By using strains of mice with genetic deficiencies of complement components and secretory IgM we have investigated the role of each complement pathway and natural IgM for innate immunity toS. pneumoniae. Our results show that the proportion of a population ofS. pneumoniaebound by C3 depends mainly on the classical pathway, whereas the intensity of C3 binding depends on the alternative pathway. Furthermore, the classical pathway, partially targeted by the binding of natural IgM to bacteria, is the dominant pathway for activation of the complement system during innate immunity toS. pneumoniae, loss of which results in rapidly progressing septicemia and impaired macrophage activation. These data demonstrate the vital role of the classical pathway for innate immunity to a bacterial pathogen.