Cutting Edge: Low-Affinity, Smith Antigen-Specific B Cells Are Tolerized by Dendritic Cells and Macrophages1

Polyclonal B cell activation promotes immunity without the loss of tolerance. Our data show that during activation of the innate immune system, B cell tolerance to Smith Ag Sm is maintained by dendritic cells (DCs) and macrophages ( M Φ ). TLR4-activated myeloid DCs and M Φ , but not plasmacytoid or...

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Bibliographic Details
Published in:The Journal of immunology (1950) 2005-07, Vol.175 (1), p.37-41
Main Authors: Kilmon, Michelle A., Rutan, Jennifer A., Clarke, Stephen H., Vilen, Barbara J.
Format: Article
Language:English
Online Access:Get full text
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Summary:Polyclonal B cell activation promotes immunity without the loss of tolerance. Our data show that during activation of the innate immune system, B cell tolerance to Smith Ag Sm is maintained by dendritic cells (DCs) and macrophages ( M Φ ). TLR4-activated myeloid DCs and M Φ , but not plasmacytoid or lymphoid DCs, repressed autoreactive B cells through the secretion of soluble mediators, including IL-6. Although IL-6 promotes plasma cell differentiation of B cells acutely stimulated by Ag, we show that it repressed cells that were chronically exposed to self-Ag. This mechanism of tolerance was not limited to Smith Ag-specific B cells as hen egg lysozyme-and p-azophenylarsonate-specific B cells were similarly affected. Our data define a tolerogenic role for M Φ and DCs in regulating autoreactive B cells during activation of the innate immune system.
ISSN:0022-1767
1550-6606