“…Originating from progenitor cells in the fetal liver and the adult bone marrow, B lymphocytes undergo multiple stages of development, and complex maturation in the peripheral lymphoid organs ( LeBien and Tedder, 2008 ; Maddaly et al, 2010 ). The broad diversity of B cell populations has increasingly been recognized, and while conventional follicular B cells are the predominant recirculating B cell population and the main source of antibody production, a variety of non-canonical B cell subsets have been described ( Haas, 2023 ) ( Figure 2 ). These include B-1 cells, an innate population of B cells found mostly in serosal cavities; marginal zone (MZ) B cells, innate B cells which can respond rapidly, in a T-cell independent manner, to blood-borne and commensal pathogens through the production of IgM and class-switched immunoglobulin G (IgG) and IgA antibodies; regulatory B cells (Bregs), a broad spectrum of B cells characterized by their ability to produce immunosuppressive cytokines; killer B cells, which express high levels of Fas-ligand and can induce apoptosis in T cells and other cell types; and age-associated B cells (ABCs), atypical memory B cell populations, characterized by expression of T-bet and CD11c, and thought to promote inflammatory responses ( Cerutti et al, 2013 ; Haas, 2023 ).…”