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PMID: 16916609 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Regulation of B cell self-tolerance by BAFF.

Seminars in immunology ·Vol. 18 ·No. 5 ·2006-10-00 ·Pages 276-83

Brink R

Abstract

To avoid the generation of pathogenic autoantibodies, self-reactive lymphocytes are deleted at several distinct checkpoints during B cell maturation. BAFF is required for mature B cell development and survival but causes B cell hyperplasia and autoimmunity when it is overexpressed. Self-reactive B cells have reduced responsiveness to BAFF and therefore die due to the limiting levels of BAFF available in vivo. Elevated BAFF expression subverts B cell self-tolerance by rescuing self-reactive B cells normally deleted relatively late during maturation. Strongly self-reactive B cells are deleted prior to expression of BAFF-R and are therefore resistant to rescue by BAFF.

MeSH Terms
Animals Apoptosis/physiology Autoimmune Diseases/etiology,immunology Autoimmunity/immunology B-Cell Activating Factor/genetics,immunology B-Cell Activation Factor Receptor/deficiency,genetics,immunology B-Lymphocyte Subsets/immunology Gene Rearrangement, B-Lymphocyte Humans Hyperplasia Lymphocyte Activation Lymphoid Tissue/immunology Mice Mice, Transgenic Models, Immunological NF-kappa B/metabolism Organ Specificity Recombinant Fusion Proteins/immunology Self Tolerance/immunology Signal Transduction
Chemicals
B-Cell Activating Factor B-Cell Activation Factor Receptor NF-kappa B Recombinant Fusion Proteins TNFRSF13C protein, human TNFSF13B protein, human Tnfrsf13c protein, mouse Tnfsf13b protein, mouse
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Brink Robert
Centenary Institute of Cancer Medicine and Cell Biology, Newtown, NSW, Australia. [email protected]
Article Info
Journal
Seminars in immunology
Abbr.
Semin Immunol
ISSN
1044-5323
Published
2006-10-00
Epub
2006-00-17
Pages
276-83
Language
English
Region
England
NLM ID
9009458
Subset
IM
Corrections
CommentIn
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