A newly identified insertion–deletion variant of the B cell activating factor (BAFF)-encoding TNFSF13B gene leads to increased levels of soluble BAFF and is associated with the development of systemic lupus erythematosus. The discovery raises a number of compelling questions for further investigation.
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Acknowledgements
The authors work is supported in part by a grant from the Alliance for Lupus Research. The author has no financial support or other benefits from commercial sources to report for the work reported in this manuscript.
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The author declares that he has acted as a consultant to Amgen (<$5,000) and Janssen Research & Development (<$5,000), has received research support from GlaxoSmithKline, and has received clinical trials support from GlaxoSmithKline and Pfizer.
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Stohl, W. BAFF emerges from the genetic shadows. Nat Rev Rheumatol 13, 456–457 (2017). https://doi.org/10.1038/nrrheum.2017.99
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DOI: https://doi.org/10.1038/nrrheum.2017.99