
The complement system of innate immunity is important in regulating humoral immunity largely through the complement receptor CR2, which forms a coreceptor on B cells during antigen-induced activation. However, CR2 also retains antigens on follicular dendritic cells (FDCs). Display of antigen on FDCs is critical for clonal selection and affinity maturation of activated B cells. This review will discuss the role of complement in adaptive immunity in general with a focus on the interplay between CR2-associated antigen on B cells with CR2 expressed on FDCs. This latter interaction provides an opportunity for memory B cells to sample antigen over prolonged periods. The cocrystal structure of CR2 with its ligand C3d provides insight into how the complement system regulates access of antigen by B cells with implications for therapeutic manipulations to modulate aberrant B cell responses in the case of autoimmunity.
CD4-Positive T-Lymphocytes, Mice, Knockout, Antigen Presentation, B-Lymphocytes, Immunology, Antigens, CD19, Autoimmunity, Lymphocyte Activation, Immunity, Innate, Immunity, Humoral, Tetraspanin 28, Mice, Infectious Diseases, Complement C3d, Immunology and Allergy, Animals, Humans, Receptors, Complement 3d, Antigens, Complement Activation, Dendritic Cells, Follicular
CD4-Positive T-Lymphocytes, Mice, Knockout, Antigen Presentation, B-Lymphocytes, Immunology, Antigens, CD19, Autoimmunity, Lymphocyte Activation, Immunity, Innate, Immunity, Humoral, Tetraspanin 28, Mice, Infectious Diseases, Complement C3d, Immunology and Allergy, Animals, Humans, Receptors, Complement 3d, Antigens, Complement Activation, Dendritic Cells, Follicular
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