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IgM memory B cells: a mouse/human paradox
Authors:Reynaud Claude-Agnès  Descatoire Marc  Dogan Ismail  Huetz François  Weller Sandra  Weill Jean-Claude
Affiliation:(1) Facult? de M?decine, Site Necker-Enfants Malades, INSERM U783 “D?veloppement du syst?me immunitaire”, Universit? Paris Descartes, 156 rue de Vaugirard, 75730 Paris Cedex 15, France;(2) Unit? de Biologie des Populations Lymphocytaires, CNRS URA 1961, Institut Pasteur, 25 rue du Docteur Roux, 75724 Paris Cedex 15, France
Abstract:Humoral memory is maintained by two types of persistent cells, memory B cells and plasma cells, which have different phenotypes and functions. Long-lived plasma cells can survive for a lifespan within a complex niche in the bone marrow and provide continuous protective serum antibody levels. Memory B cells reside in secondary lymphoid organs, where they can be rapidly mobilized upon a new antigenic encounter. Surface IgG has long been taken as a surrogate marker for memory in the mouse. Recently, however, we have brought evidence for a long-lived IgM memory B cell population in the mouse, while we have also argued that, in humans, these same cells are not classical memory B cells but marginal zone (MZ) B cells which, as opposed to their mouse MZ counterpart, recirculate and carry a mutated B cell receptor. In this review, we will discuss these apparently paradoxical results.
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