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Predominant Autoantibody Production by Early Human B Cell Precursors

Wardemann, Hedda, Yurasov, Sergey, Schaefer, Anne, Young, James W., Meffre, Eric, Nussenzweig, Michel C.·2003·Science

Abstract

During B lymphocyte development, antibodies are assembled by random gene segment reassortment to produce a vast number of specificities. A potential disadvantage of this process is that some of the antibodies produced are self-reactive. We determined the prevalence of self-reactive antibody formation and its regulation in human B cells. A majority (55 to 75%) of all antibodies expressed by early immature B cells displayed self-reactivity, including polyreactive and anti-nuclear specificities. Most of these autoantibodies were removed from the population at two discrete checkpoints during B cell development. Inefficient checkpoint regulation would lead to substantial increases in circulating autoantibodies.

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Metadata

Authors
Wardemann, H., Yurasov, S., Schaefer, A., Young, J. W., Meffre, E., & Nussenzweig, M. C.
Venue
Science
Published
2003-09-05
Volume
301
Issue
5638
Pages
1374-1377
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2076198413
Cited by
2,083
References
0
FWCI
16.54
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Predominant Autoantibody Production by Early Human B Cell Precursors. https://app.cochat.ai/papers/10.1126/science.1086907
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Wardemann, H., Yurasov, S., Schaefer, A., Young, J. W., Meffre, E., & Nussenzweig, M. C. (2003). Predominant Autoantibody Production by Early Human B Cell Precursors. Science. https://doi.org/10.1126/science.1086907

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.