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pubmed-article:17306569pubmed:abstractTextMore than half of the nascent B cells in humans initially express autoreactive antibodies. However, most of these autoantibodies are removed from the repertoire at two checkpoints before maturation into naive B cells. A third checkpoint excludes remaining autoantibodies from the antigen-experienced IgM(+) memory B cell pool. Nevertheless, low-affinity self-reactive antibodies are frequently found in the serum of normal humans. To determine the source of these antibodies, we cloned and expressed antibodies from circulating human IgG(+) memory B cells. Surprisingly, we found that self-reactive antibodies including anti-nuclear antibodies were frequently expressed by IgG(+) memory B cells in healthy donors. Most of these antibodies were created de novo by somatic hypermutation during the transition between mature naive and IgG(+) memory B cells. We conclude that deregulation of self-reactive IgG(+) memory B cells may be associated with autoimmunity.lld:pubmed
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pubmed-article:17306569pubmed:authorpubmed-author:NussenzweigMi...lld:pubmed
pubmed-article:17306569pubmed:authorpubmed-author:WardemannHedd...lld:pubmed
pubmed-article:17306569pubmed:authorpubmed-author:TsuijiMakotoMlld:pubmed
pubmed-article:17306569pubmed:authorpubmed-author:VelinzonKlara...lld:pubmed
pubmed-article:17306569pubmed:authorpubmed-author:YurasovSergey...lld:pubmed
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pubmed-article:17306569pubmed:dateRevised2011-6-1lld:pubmed
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pubmed-article:17306569pubmed:articleTitleAutoreactivity in human IgG+ memory B cells.lld:pubmed
pubmed-article:17306569pubmed:affiliationMax-Planck-Institute for Infection Biology, D-10117 Berlin, Germany.lld:pubmed
pubmed-article:17306569pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:17306569pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
pubmed-article:17306569pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed