Plasma cell differentiation during the germinal center reaction
Wataru Ise, Tomohiro Kurosaki
Abstract
Wataru Ise, Tomohiro Kurosaki
Abstract
Germinal centers (GCs) are formed in secondary lymphoid tissues upon immunization with T-dependent antigens. In GCs, somatic hypermutation generates B cells with increased antibody affinity and these high-affinity B cells preferentially differentiate into plasma cells, which home to bone marrow and confer long-lived humoral immunity. Recent studies have shed new light on the cellular and molecular basis for initiating the transition from a GC B cell to a plasma cell. Here, we review recent progress in our understanding of how plasma cell generation during the GC reaction is regulated for inducing effective long-term protective immunity and for preventing harmful autoimmunity.
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Germinal centers (GCs) are formed in secondary lymphoid tissues upon immunization with T-dependent antigens. In GCs, somatic hypermutation generates B cells with increased antibody affinity and these high-affinity B cells preferentially differentiate into plasma cells, which home to bone marrow and confer long-lived humoral immunity. Recent studies have shed new light on the cellular and molecular basis for initiating the transition from a GC B cell to a plasma cell. Here, we review recent progress in our understanding of how plasma cell generation during the GC reaction is regulated for inducing effective long-term protective immunity and for preventing harmful autoimmunity.
Key concepts: Germinal center, Somatic hypermutation, Plasma cell, Biology, B cell, Autoimmunity, Immunology, Antibody