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Diversification of memory B cells drives the continuous adaptation of secretory antibodies to gut microbiota
Diversification of memory B cells drives the continuous adaptation of secretory antibodies to gut microbiota
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Diversification of memory B cells drives the continuous adaptation of secretory antibodies to gut microbiota
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Diversification of memory B cells drives the continuous adaptation of secretory antibodies to gut microbiota
Diversification of memory B cells drives the continuous adaptation of secretory antibodies to gut microbiota

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Diversification of memory B cells drives the continuous adaptation of secretory antibodies to gut microbiota
Diversification of memory B cells drives the continuous adaptation of secretory antibodies to gut microbiota
Journal Article

Diversification of memory B cells drives the continuous adaptation of secretory antibodies to gut microbiota

2015
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Overview
Secretory IgA (SIgA) shapes the gut microbial composition. Pabst and colleagues show that the IgA-secreting plasma cell repertoire, once established, is remarkably resilient to changes in microbial populations that occur upon infection or antibiotic treatment. Secretory immunoglobulin A (SIgA) shields the gut epithelium from luminal antigens and contributes to host-microbe symbiosis. However, how antibody responses are regulated to achieve sustained host-microbe interactions is unknown. We found that mice and humans exhibited longitudinal persistence of clonally related B cells in the IgA repertoire despite major changes in the microbiota during antibiotic treatment or infection. Memory B cells recirculated between inductive compartments and were clonally related to plasma cells in gut and mammary glands. Our findings suggest that continuous diversification of memory B cells constitutes a central process for establishing symbiotic host-microbe interactions and offer an explanation of how maternal antibodies are optimized throughout life to protect the newborn.