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Colonization by the microbiota significantly stimulates B cells and induces immunoglobulin production. Mammals colonized with various taxa develop highly complex and individualized immunoglobulin repertoires (IgA and IgG Repertoire).
The IgA repertoire, which predominantly targets cell-surface antigens, did not expand after baxterial dose escalation.
Increased systemic exposure broadened the IgG repertoire to include both microbial cytoplasmic and cell-surface antigens.
Microbial exposures induced characteristic immunoglobulin heavy-chain repertoires in B cells, primarily at the memory and plasma cell stages. The responses varied based on the type of exposure: