Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3345990 | Current Opinion in Immunology | 2013 | 5 Pages |
•Multiple memory B-cell subsets are generated by the immune response.•IgM+ and IgG+ memory B cells fullfill different effector functions.•Early memory B cells emerge as germinal center-independent subpopulations.•Persisting germinal centers modify the outcome of the recall response.
B cell memory has long been considered the attribute of the sole IgG-positive B cell subset. Since a few years, and due to new B-cell subset identification procedures, increasing heterogeneity has been identified among the memory B cell pool. IgM-positive cells and germinal center-independent subsets are recent additions to the field. This review describes the diversity of memory B cells, as well as controversial issues on their relative contribution to the recall response. The impact of a protracted germinal center response to the specific mobilization of IgM memory B cells is proposed.