Early preplasma cells define a tolerance checkpoint for autoreactive B cells
DA Culton, BP O'Conner, KL Conway, R Diz… - The Journal of …, 2006 - journals.aai.org
DA Culton, BP O'Conner, KL Conway, R Diz, J Rutan, BJ Vilen, SH Clarke
The Journal of Immunology, 2006•journals.aai.orgAb-secreting plasma cells (PCs) are the effectors of humoral immunity. In this study, we
describe regulation of autoreactive B cells specific for the ribonucleoprotein Smith (Sm) at an
early pre-PC stage. These cells are defined by the expression of the PC marker CD138 and
normal levels of CD19 and B220. They are present at a high frequency in normal mouse
spleen and bone marrow, are Ag dependent, and are located predominantly along the T cell-
B cell border and near bridging channels. Anti-Sm pre-PCs also occur at a high frequency in …
describe regulation of autoreactive B cells specific for the ribonucleoprotein Smith (Sm) at an
early pre-PC stage. These cells are defined by the expression of the PC marker CD138 and
normal levels of CD19 and B220. They are present at a high frequency in normal mouse
spleen and bone marrow, are Ag dependent, and are located predominantly along the T cell-
B cell border and near bridging channels. Anti-Sm pre-PCs also occur at a high frequency in …
Abstract
Ab-secreting plasma cells (PCs) are the effectors of humoral immunity. In this study, we describe regulation of autoreactive B cells specific for the ribonucleoprotein Smith (Sm) at an early pre-PC stage. These cells are defined by the expression of the PC marker CD138 and normal levels of CD19 and B220. They are present at a high frequency in normal mouse spleen and bone marrow, are Ag dependent, and are located predominantly along the T cell-B cell border and near bridging channels. Anti-Sm pre-PCs also occur at a high frequency in nonautoimmune mice and show additional phenotypic characteristics of PC differentiation. However, while some of these pre-PCs are Ab-secreting cells, those specific for Sm are not, indicating regulation. Consistent with this, anti-Sm pre-PCs have a higher turnover rate and higher frequency of cell death than those that do not bind Sm. Regulation of anti-Sm pre-PCs occurs upstream of the transcriptional repressor, B lymphocyte-induced maturation protein-1, expression. Regulation at this stage is overcome in autoimmune MRL/lpr mice and is accompanied by an altered B lymphocyte stimulator receptor profile. These data reveal a new B cell tolerance checkpoint that is overcome in autoimmunity.
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