MacLean, A. J.; Deimel, L. P.; Zhou, P.; ElTanbouly, M. A.; Merkenschlager, J.; Ramos, V.; Santos, G. S.; Hagglof, T.; Mayer, C. T.; Hernandez, B.; Gazumyan, A.; Nussenzweig, M. C.

Increased antibody affinity over time after vaccination, known as affinity maturation, is a prototypical feature of immune responses. Recent studies have shown that a diverse collection of B cells, producing antibodies with a wide spectrum of different affinities, are selected into the plasma cell (PC) pathway. How affinity-permissive selection enables PC affinity maturation remains unknown. Here we report that PC precursors (prePC) expressing high affinity antibodies receive higher levels of T follicular helper (Tfh)-derived help and divide at higher rates than their lower affinity counterparts once they leave the GC. Thus, differential cell division by selected prePCs accounts for how diverse precursors develop into a PC compartment that mediates serological affinity maturation.