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Germinal centre (GC) B cells undergo rapid proliferation, somatic hypermutation, and selection while delaying terminal differentiation and apoptosis. BCL6 is highly expressed in GC B cells and functions as a transcriptional repressor of genes involved in DNA damage responses, cell-cycle arrest, and plasma cell differentiation. In experimental systems where BCL6 is selectively deleted in B cells, germinal centres fail to form and antibody affinity maturation is severely impaired.
Based on these findings, what is the most likely
primary role of BCL6 in shaping B‑cell responses?