Local BLyS production by T follicular cells mediates retention of high affinity B cells during affinity maturation

Author:

Goenka Radhika1,Matthews Andrew H.1,Zhang Bochao2,O’Neill Patrick J.1,Scholz Jean L.1,Migone Thi-Sau3,Leonard Warren J.4,Stohl William5,Hershberg Uri2,Cancro Michael P.1

Affiliation:

1. Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104

2. School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA 19104

3. Human Genome Sciences, Inc., Rockville, MD 20850

4. Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, Bethesda, MD 20892

5. Division of Rheumatology, University of Southern California Keck School of Medicine, Los Angeles, CA 90033

Abstract

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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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