We have assessed the role of B lymphocyte stimulator (BLyS) and its receptors in the germinal center (GC) reaction and affinity maturation. Despite ample BLyS retention on B cells in follicular (FO) regions, the GC microenvironment lacks substantial BLyS. This reflects IL-21-mediated down-regulation of the BLyS receptor TACI (transmembrane activator and calcium modulator and cyclophilin ligand interactor) on GC B cells, thus limiting their capacity for BLyS binding and retention. Within the GC, FO helper T cells (TFH cells) provide a local source of BLyS. Whereas T cell-derived BLyS is dispensable for normal GC cellularity and somatic hypermutation, it is required for the efficient selection of high affinity GC B cell clones. These findings suggest that during affinity maturation, high affinity clones rely on TFH-derived BLyS for their persistence. © 2014 Goenka et al.
CITATION STYLE
Goenka, R., Matthews, A. H., Zhang, B., O’Neill, P. J., Scholz, J. L., Migone, T. S., … Cancro, M. P. (2014). Local BLyS production by T follicular cells mediates retention of high affinity B cells during affinity maturation. Journal of Experimental Medicine, 211(1), 45–56. https://doi.org/10.1084/jem.20130505
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