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Functional diversity within the memory B cell pool is established through interactions between memory B cells and the environment in which they develop and reside. This review will discuss novel insights into the role of cytokines encountered in the microenvironment in modulating memory B cell transcriptomic, epigenetic, and phenotypic identity. Specifically, it will focus on how interferons can prime unique memory B cell subpopulations upregulated in chronic viral infection, autoimmunity, and cancer. 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