After antigen contact, B cells rapidly differentiate and cycle through several phenotypical intermediaries before entering 1 of 2 longer-lived stages, the memory B cell or the plasma cell. In this issue of Blood, van Keimpema et al identify a role for the forkhead transcription factor FOXP1 in inhibiting the very last differentiation stage: plasma cell differentiation. They show that FOXP1 directly represses several key regulators of plasma cell differentiation. Although FOXP1 is strongly expressed in naïve B cells, it is lost as B cells enter germinal center differentiation. However, it is re-expressed in memory B cells where it correlates with immunoglobulin class switch recombination status, with immunoglobulin (Ig)G-switched memory B cells expressing lower levels of FOXP1. Interestingly, this correlates with a trait of IgG-switched memory B cells to being more likely to enter plasma cell differentiation3 (see figure).
CITATION STYLE
Toellner, K. M. (2015, October 29). FOXP1 inhibits plasma cell differentiation. Blood. American Society of Hematology. https://doi.org/10.1182/blood-2015-09-666529
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