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The site and stage of anti-DNA B-cell deletion
Journal article   Open access   Peer reviewed

The site and stage of anti-DNA B-cell deletion

Ching Chen, Zoltan Nagy, Marko Radic, Richard Hardy and Chaomei Chen
Nature (London), v 373(6511)
19 Jan 1995
PMID: 7816141
url
https://hdl.handle.net/2027.42/62909View

Abstract

Bone marrow Cellular biology Deoxyribonucleic acid DNA Medical immunity Rodents
Antibodies to DNA and nucleoproteins are found in sera of individuals with systemic autoimmune disease. In the population (and in the autoimmune mouse strain MRL/lpr) there is a great variety of such antinuclear antibodies, but individuals with systemic lupus erythematosus or single MRL mice express a subset only of the antinuclear specificities found in the population. These observations have been interpreted to mean that these antibodies arise by immunization. The oligoclonal nature of the autoantibody response and the evidence of selection acting on somatically mutated autoantibodies favour this interpretation. Specific activation of autoantibodies in disease implies either that autoantibodies are regulated in non-diseased individuals or that autoantigen availability is variable. The former has been demonstrated in anti-DNA transgenic mice. In normal mice, transgene-encoded antibodies against double-stranded (ds) DNA are not expressed in serum or on B cells. Here we describe modified anti-dsDNA transgenic mice which allow us to study the site and developmental stage at which such B-cell regulation occurs. This model shows that in normal mice B cells expressing anti-DNA specificity are deleted in the bone marrow at a pre-B to immature B transitional stage.

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Collaboration types
Domestic collaboration
Web of Science research areas
Immunology
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