Class-switched memory B cells remodel BCRs within secondary germinal centers

• Published in: Nature immunology Vol. 16; no. 3; pp. 296 - 305
• Main Authors: McHeyzer-Williams, Louise J, Milpied, Pierre J, Okitsu, Shinji L, McHeyzer-Williams, Michael G
• Format: Journal Article
• Language: English
• Published: New York Nature Publishing Group US 01.03.2015; Nature Publishing Group
• Subjects: 13/31; 13/51; 38/23; 38/39; 38/62; 38/77; 631/250/1619/40; 631/250/1619/40/1774; 631/250/2152; Animals; Antibodies - immunology; Antibody Formation - immunology; Antigens, CD - immunology; B cells; B-Lymphocytes - immunology; Biomedicine; CD83 Antigen; DNA-Directed DNA Polymerase - immunology; Germinal Center - immunology; Immunoglobulin Class Switching - immunology; Immunoglobulins - immunology; Immunologic Memory - immunology; Immunology; Infectious Diseases; Membrane Glycoproteins - immunology; Mice; Mice, Inbred C57BL; Physiological aspects; Physiological research; Receptors, Antigen, B-Cell - immunology; Transcription, Genetic - immunology; Vaccines
• ISSN: 1529-2908; 1529-2916
• DOI: 10.1038/ni.3095

The mechanisms of secondary changes in antibody repertoires remain unclear. McHeyzer-Williams and colleagues define the stages of reentry of class-switched memory B cells into germinal centers to remodel existing antibody specificities. Effective vaccines induce high-affinity memory B cells and durable antibody responses through accelerated mechanisms of natural selection. Secondary changes in antibody repertoires after vaccine boosts suggest progressive rediversification of B cell receptors (BCRs), but the underlying mechanisms remain unresolved. Here, the integrated specificity and function of individual memory B cell progeny revealed ongoing evolution of polyclonal antibody specificities through germinal center (GC)-specific transcriptional activity. At the clonal and subclonal levels, single-cell expression of the genes encoding the costimulatory molecule CD83 and the DNA polymerase Polη segregated the secondary GC transcriptional program into four stages that regulated divergent mechanisms of memory BCR evolution. Our studies demonstrate that vaccine boosts reactivate a cyclic program of GC function in class-switched memory B cells to remodel existing antibody specificities and enhance durable immunological protection.